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Null and Alternative Hypotheses | Definitions & Examples

Published on 5 October 2022 by Shaun Turney . Revised on 6 December 2022.

The null and alternative hypotheses are two competing claims that researchers weigh evidence for and against using a statistical test :

  • Null hypothesis (H 0 ): There’s no effect in the population .
  • Alternative hypothesis (H A ): There’s an effect in the population.

The effect is usually the effect of the independent variable on the dependent variable .

Table of contents

Answering your research question with hypotheses, what is a null hypothesis, what is an alternative hypothesis, differences between null and alternative hypotheses, how to write null and alternative hypotheses, frequently asked questions about null and alternative hypotheses.

The null and alternative hypotheses offer competing answers to your research question . When the research question asks “Does the independent variable affect the dependent variable?”, the null hypothesis (H 0 ) answers “No, there’s no effect in the population.” On the other hand, the alternative hypothesis (H A ) answers “Yes, there is an effect in the population.”

The null and alternative are always claims about the population. That’s because the goal of hypothesis testing is to make inferences about a population based on a sample . Often, we infer whether there’s an effect in the population by looking at differences between groups or relationships between variables in the sample.

You can use a statistical test to decide whether the evidence favors the null or alternative hypothesis. Each type of statistical test comes with a specific way of phrasing the null and alternative hypothesis. However, the hypotheses can also be phrased in a general way that applies to any test.

The null hypothesis is the claim that there’s no effect in the population.

If the sample provides enough evidence against the claim that there’s no effect in the population ( p ≤ α), then we can reject the null hypothesis . Otherwise, we fail to reject the null hypothesis.

Although “fail to reject” may sound awkward, it’s the only wording that statisticians accept. Be careful not to say you “prove” or “accept” the null hypothesis.

Null hypotheses often include phrases such as “no effect”, “no difference”, or “no relationship”. When written in mathematical terms, they always include an equality (usually =, but sometimes ≥ or ≤).

Examples of null hypotheses

The table below gives examples of research questions and null hypotheses. There’s always more than one way to answer a research question, but these null hypotheses can help you get started.

*Note that some researchers prefer to always write the null hypothesis in terms of “no effect” and “=”. It would be fine to say that daily meditation has no effect on the incidence of depression and p 1 = p 2 .

The alternative hypothesis (H A ) is the other answer to your research question . It claims that there’s an effect in the population.

Often, your alternative hypothesis is the same as your research hypothesis. In other words, it’s the claim that you expect or hope will be true.

The alternative hypothesis is the complement to the null hypothesis. Null and alternative hypotheses are exhaustive, meaning that together they cover every possible outcome. They are also mutually exclusive, meaning that only one can be true at a time.

Alternative hypotheses often include phrases such as “an effect”, “a difference”, or “a relationship”. When alternative hypotheses are written in mathematical terms, they always include an inequality (usually ≠, but sometimes > or <). As with null hypotheses, there are many acceptable ways to phrase an alternative hypothesis.

Examples of alternative hypotheses

The table below gives examples of research questions and alternative hypotheses to help you get started with formulating your own.

Null and alternative hypotheses are similar in some ways:

  • They’re both answers to the research question
  • They both make claims about the population
  • They’re both evaluated by statistical tests.

However, there are important differences between the two types of hypotheses, summarized in the following table.

To help you write your hypotheses, you can use the template sentences below. If you know which statistical test you’re going to use, you can use the test-specific template sentences. Otherwise, you can use the general template sentences.

The only thing you need to know to use these general template sentences are your dependent and independent variables. To write your research question, null hypothesis, and alternative hypothesis, fill in the following sentences with your variables:

Does independent variable affect dependent variable ?

  • Null hypothesis (H 0 ): Independent variable does not affect dependent variable .
  • Alternative hypothesis (H A ): Independent variable affects dependent variable .

Test-specific

Once you know the statistical test you’ll be using, you can write your hypotheses in a more precise and mathematical way specific to the test you chose. The table below provides template sentences for common statistical tests.

Note: The template sentences above assume that you’re performing one-tailed tests . One-tailed tests are appropriate for most studies.

The null hypothesis is often abbreviated as H 0 . When the null hypothesis is written using mathematical symbols, it always includes an equality symbol (usually =, but sometimes ≥ or ≤).

The alternative hypothesis is often abbreviated as H a or H 1 . When the alternative hypothesis is written using mathematical symbols, it always includes an inequality symbol (usually ≠, but sometimes < or >).

A research hypothesis is your proposed answer to your research question. The research hypothesis usually includes an explanation (‘ x affects y because …’).

A statistical hypothesis, on the other hand, is a mathematical statement about a population parameter. Statistical hypotheses always come in pairs: the null and alternative hypotheses. In a well-designed study , the statistical hypotheses correspond logically to the research hypothesis.

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9.1: Null and Alternative Hypotheses

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The actual test begins by considering two hypotheses . They are called the null hypothesis and the alternative hypothesis . These hypotheses contain opposing viewpoints.

\(H_0\): The null hypothesis: It is a statement of no difference between the variables—they are not related. This can often be considered the status quo and as a result if you cannot accept the null it requires some action.

\(H_a\): The alternative hypothesis: It is a claim about the population that is contradictory to \(H_0\) and what we conclude when we reject \(H_0\). This is usually what the researcher is trying to prove.

Since the null and alternative hypotheses are contradictory, you must examine evidence to decide if you have enough evidence to reject the null hypothesis or not. The evidence is in the form of sample data.

After you have determined which hypothesis the sample supports, you make a decision. There are two options for a decision. They are "reject \(H_0\)" if the sample information favors the alternative hypothesis or "do not reject \(H_0\)" or "decline to reject \(H_0\)" if the sample information is insufficient to reject the null hypothesis.

\(H_{0}\) always has a symbol with an equal in it. \(H_{a}\) never has a symbol with an equal in it. The choice of symbol depends on the wording of the hypothesis test. However, be aware that many researchers (including one of the co-authors in research work) use = in the null hypothesis, even with > or < as the symbol in the alternative hypothesis. This practice is acceptable because we only make the decision to reject or not reject the null hypothesis.

Example \(\PageIndex{1}\)

  • \(H_{0}\): No more than 30% of the registered voters in Santa Clara County voted in the primary election. \(p \leq 30\)
  • \(H_{a}\): More than 30% of the registered voters in Santa Clara County voted in the primary election. \(p > 30\)

Exercise \(\PageIndex{1}\)

A medical trial is conducted to test whether or not a new medicine reduces cholesterol by 25%. State the null and alternative hypotheses.

  • \(H_{0}\): The drug reduces cholesterol by 25%. \(p = 0.25\)
  • \(H_{a}\): The drug does not reduce cholesterol by 25%. \(p \neq 0.25\)

Example \(\PageIndex{2}\)

We want to test whether the mean GPA of students in American colleges is different from 2.0 (out of 4.0). The null and alternative hypotheses are:

  • \(H_{0}: \mu = 2.0\)
  • \(H_{a}: \mu \neq 2.0\)

Exercise \(\PageIndex{2}\)

We want to test whether the mean height of eighth graders is 66 inches. State the null and alternative hypotheses. Fill in the correct symbol \((=, \neq, \geq, <, \leq, >)\) for the null and alternative hypotheses.

  • \(H_{0}: \mu \_ 66\)
  • \(H_{a}: \mu \_ 66\)
  • \(H_{0}: \mu = 66\)
  • \(H_{a}: \mu \neq 66\)

Example \(\PageIndex{3}\)

We want to test if college students take less than five years to graduate from college, on the average. The null and alternative hypotheses are:

  • \(H_{0}: \mu \geq 5\)
  • \(H_{a}: \mu < 5\)

Exercise \(\PageIndex{3}\)

We want to test if it takes fewer than 45 minutes to teach a lesson plan. State the null and alternative hypotheses. Fill in the correct symbol ( =, ≠, ≥, <, ≤, >) for the null and alternative hypotheses.

  • \(H_{0}: \mu \_ 45\)
  • \(H_{a}: \mu \_ 45\)
  • \(H_{0}: \mu \geq 45\)
  • \(H_{a}: \mu < 45\)

Example \(\PageIndex{4}\)

In an issue of U. S. News and World Report , an article on school standards stated that about half of all students in France, Germany, and Israel take advanced placement exams and a third pass. The same article stated that 6.6% of U.S. students take advanced placement exams and 4.4% pass. Test if the percentage of U.S. students who take advanced placement exams is more than 6.6%. State the null and alternative hypotheses.

  • \(H_{0}: p \leq 0.066\)
  • \(H_{a}: p > 0.066\)

Exercise \(\PageIndex{4}\)

On a state driver’s test, about 40% pass the test on the first try. We want to test if more than 40% pass on the first try. Fill in the correct symbol (\(=, \neq, \geq, <, \leq, >\)) for the null and alternative hypotheses.

  • \(H_{0}: p \_ 0.40\)
  • \(H_{a}: p \_ 0.40\)
  • \(H_{0}: p = 0.40\)
  • \(H_{a}: p > 0.40\)

COLLABORATIVE EXERCISE

Bring to class a newspaper, some news magazines, and some Internet articles . In groups, find articles from which your group can write null and alternative hypotheses. Discuss your hypotheses with the rest of the class.

In a hypothesis test , sample data is evaluated in order to arrive at a decision about some type of claim. If certain conditions about the sample are satisfied, then the claim can be evaluated for a population. In a hypothesis test, we:

  • Evaluate the null hypothesis , typically denoted with \(H_{0}\). The null is not rejected unless the hypothesis test shows otherwise. The null statement must always contain some form of equality \((=, \leq \text{or} \geq)\)
  • Always write the alternative hypothesis , typically denoted with \(H_{a}\) or \(H_{1}\), using less than, greater than, or not equals symbols, i.e., \((\neq, >, \text{or} <)\).
  • If we reject the null hypothesis, then we can assume there is enough evidence to support the alternative hypothesis.
  • Never state that a claim is proven true or false. Keep in mind the underlying fact that hypothesis testing is based on probability laws; therefore, we can talk only in terms of non-absolute certainties.

Formula Review

\(H_{0}\) and \(H_{a}\) are contradictory.

  • If \(\alpha \leq p\)-value, then do not reject \(H_{0}\).
  • If\(\alpha > p\)-value, then reject \(H_{0}\).

\(\alpha\) is preconceived. Its value is set before the hypothesis test starts. The \(p\)-value is calculated from the data.References

Data from the National Institute of Mental Health. Available online at http://www.nimh.nih.gov/publicat/depression.cfm .

Null Hypothesis Examples

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In statistical analysis, the null hypothesis assumes there is no meaningful relationship between two variables. Testing the null hypothesis can tell you whether your results are due to the effect of manipulating ​a dependent variable or due to chance. It's often used in conjunction with an alternative hypothesis, which assumes there is, in fact, a relationship between two variables.

The null hypothesis is among the easiest hypothesis to test using statistical analysis, making it perhaps the most valuable hypothesis for the scientific method. By evaluating a null hypothesis in addition to another hypothesis, researchers can support their conclusions with a higher level of confidence. Below are examples of how you might formulate a null hypothesis to fit certain questions.

What Is the Null Hypothesis?

The null hypothesis states there is no relationship between the measured phenomenon (the dependent variable ) and the independent variable , which is the variable an experimenter typically controls or changes. You do not​ need to believe that the null hypothesis is true to test it. On the contrary, you will likely suspect there is a relationship between a set of variables. One way to prove that this is the case is to reject the null hypothesis. Rejecting a hypothesis does not mean an experiment was "bad" or that it didn't produce results. In fact, it is often one of the first steps toward further inquiry.

To distinguish it from other hypotheses , the null hypothesis is written as ​ H 0  (which is read as “H-nought,” "H-null," or "H-zero"). A significance test is used to determine the likelihood that the results supporting the null hypothesis are not due to chance. A confidence level of 95% or 99% is common. Keep in mind, even if the confidence level is high, there is still a small chance the null hypothesis is not true, perhaps because the experimenter did not account for a critical factor or because of chance. This is one reason why it's important to repeat experiments.

Examples of the Null Hypothesis

To write a null hypothesis, first start by asking a question. Rephrase that question in a form that assumes no relationship between the variables. In other words, assume a treatment has no effect. Write your hypothesis in a way that reflects this.

Other Types of Hypotheses

In addition to the null hypothesis, the alternative hypothesis is also a staple in traditional significance tests . It's essentially the opposite of the null hypothesis because it assumes the claim in question is true. For the first item in the table above, for example, an alternative hypothesis might be "Age does have an effect on mathematical ability."

Key Takeaways

  • In hypothesis testing, the null hypothesis assumes no relationship between two variables, providing a baseline for statistical analysis.
  • Rejecting the null hypothesis suggests there is evidence of a relationship between variables.
  • By formulating a null hypothesis, researchers can systematically test assumptions and draw more reliable conclusions from their experiments.
  • Difference Between Independent and Dependent Variables
  • Examples of Independent and Dependent Variables
  • What Is a Hypothesis? (Science)
  • What 'Fail to Reject' Means in a Hypothesis Test
  • Definition of a Hypothesis
  • Null Hypothesis Definition and Examples
  • Scientific Method Vocabulary Terms
  • Null Hypothesis and Alternative Hypothesis
  • Hypothesis Test for the Difference of Two Population Proportions
  • How to Conduct a Hypothesis Test
  • What Is a P-Value?
  • What Are the Elements of a Good Hypothesis?
  • What Is the Difference Between Alpha and P-Values?
  • Understanding Path Analysis
  • Hypothesis Test Example
  • An Example of a Hypothesis Test

Null Hypothesis

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  • pp 3267–3270
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null hypothesis on research

  • Tom Booth 3 ,
  • Alex Doumas 3 &
  • Aja Louise Murray 4  

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In formal hypothesis testing, the null hypothesis ( H 0 ) is the hypothesis assumed to be true in the population and which gives rise to the sampling distribution of the test statistic in question (Hays 1994 ). The critical feature of the null hypothesis across hypothesis testing frameworks is that it is stated with enough precision that it can be tested.

Introduction

A hypothesis is a statement or explanation about the nature or causes of some phenomena of interest. In the process of scientific study, we can distinguish two forms of hypotheses. A research hypothesis poses the question of interest, and if well stated, will include the variables under study and the expected relationship between them. A statistical hypothesis translates the research hypothesis into a mathematically precise, statistically testable statement concerning the assumed value of a parameter of interest in the population. The null hypothesis is an example of a statistical hypothesis.

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Fisher, R. (1925). Statistical methods for research workers (1st ed.). Edinburgh: Oliver and Boyd.

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Gigerenzer, G. (2004). Mindless statistics. The Journal of Socio-Economics, 33 , 587–606.

Article   Google Scholar  

Hays, W. L. (1994). Statistics (5th ed.). Belmont: Wadsworth.

Neyman, J., & Pearson, E. S. (1933). On the problem of the most efficient tests of statistical hypotheses. Philosophical Transactions of the Royal Society of London, Series A, 231 , 289–337.

Szucs, D., & Ioannidis, J. P. A. (2016). When null hypothesis significance testing is unsuitable for research: A reassessment. bioRxiv . https://doi.org/10.1101/095570 .

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Booth, T., Doumas, A., Murray, A.L. (2020). Null Hypothesis. In: Zeigler-Hill, V., Shackelford, T.K. (eds) Encyclopedia of Personality and Individual Differences. Springer, Cham. https://doi.org/10.1007/978-3-319-24612-3_1335

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What is Null Hypothesis? What Is Its Importance in Research?

' src=

Scientists begin their research with a hypothesis that a relationship of some kind exists between variables. The null hypothesis is the opposite stating that no such relationship exists. Null hypothesis may seem unexciting, but it is a very important aspect of research. In this article, we discuss what null hypothesis is, how to make use of it, and why you should use it to improve your statistical analyses.

What is the Null Hypothesis?

The null hypothesis can be tested using statistical analysis  and is often written as H 0 (read as “H-naught”). Once you determine how likely the sample relationship would be if the H 0   were true, you can run your analysis. Researchers use a significance test to determine the likelihood that the results supporting the H 0 are not due to chance.

The null hypothesis is not the same as an alternative hypothesis. An alternative hypothesis states, that there is a relationship between two variables, while H 0 posits the opposite. Let us consider the following example.

A researcher wants to discover the relationship between exercise frequency and appetite. She asks:

Q: Does increased exercise frequency lead to increased appetite? Alternative hypothesis: Increased exercise frequency leads to increased appetite. H 0 assumes that there is no relationship between the two variables: Increased exercise frequency does not lead to increased appetite.

Let us look at another example of how to state the null hypothesis:

Q: Does insufficient sleep lead to an increased risk of heart attack among men over age 50? H 0 : The amount of sleep men over age 50 get does not increase their risk of heart attack.

Why is Null Hypothesis Important?

Many scientists often neglect null hypothesis in their testing. As shown in the above examples, H 0 is often assumed to be the opposite of the hypothesis being tested. However, it is good practice to include H 0 and ensure it is carefully worded. To understand why, let us return to our previous example. In this case,

Alternative hypothesis: Getting too little sleep leads to an increased risk of heart attack among men over age 50.

H 0 : The amount of sleep men over age 50 get has no effect on their risk of heart attack.

Note that this H 0 is different than the one in our first example. What if we were to conduct this experiment and find that neither H 0 nor the alternative hypothesis was supported? The experiment would be considered invalid . Take our original H 0 in this case, “the amount of sleep men over age 50 get, does not increase their risk of heart attack”. If this H 0 is found to be untrue, and so is the alternative, we can still consider a third hypothesis. Perhaps getting insufficient sleep actually decreases the risk of a heart attack among men over age 50. Because we have tested H 0 , we have more information that we would not have if we had neglected it.

Do I Really Need to Test It?

The biggest problem with the null hypothesis is that many scientists see accepting it as a failure of the experiment. They consider that they have not proven anything of value. However, as we have learned from the replication crisis , negative results are just as important as positive ones. While they may seem less appealing to publishers, they can tell the scientific community important information about correlations that do or do not exist. In this way, they can drive science forward and prevent the wastage of resources.

Do you test for the null hypothesis? Why or why not? Let us know your thoughts in the comments below.

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The following null hypotheses were formulated for this study: Ho1. There are no significant differences in the factors that influence urban gardening when respondents are grouped according to age, sex, household size, social status and average combined monthly income.

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Once you have developed a clear and focused research question or set of research questions, you’ll be ready to conduct further research, a literature review, on the topic to help you make an educated guess about the answer to your question(s). This educated guess is called a hypothesis.

In research, there are two types of hypotheses: null and alternative. They work as a complementary pair, each stating that the other is wrong.

  • Null Hypothesis (H 0 ) – This can be thought of as the implied hypothesis. “Null” meaning “nothing.”  This hypothesis states that there is no difference between groups or no relationship between variables. The null hypothesis is a presumption of status quo or no change.
  • Alternative Hypothesis (H a ) – This is also known as the claim. This hypothesis should state what you expect the data to show, based on your research on the topic. This is your answer to your research question.

Null Hypothesis:   H 0 : There is no difference in the salary of factory workers based on gender. Alternative Hypothesis :  H a : Male factory workers have a higher salary than female factory workers.

Null Hypothesis :  H 0 : There is no relationship between height and shoe size. Alternative Hypothesis :  H a : There is a positive relationship between height and shoe size.

Null Hypothesis :  H 0 : Experience on the job has no impact on the quality of a brick mason’s work. Alternative Hypothesis :  H a : The quality of a brick mason’s work is influenced by on-the-job experience.

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Chapter 13: Inferential Statistics

Understanding Null Hypothesis Testing

Learning Objectives

  • Explain the purpose of null hypothesis testing, including the role of sampling error.
  • Describe the basic logic of null hypothesis testing.
  • Describe the role of relationship strength and sample size in determining statistical significance and make reasonable judgments about statistical significance based on these two factors.

The Purpose of Null Hypothesis Testing

As we have seen, psychological research typically involves measuring one or more variables for a sample and computing descriptive statistics for that sample. In general, however, the researcher’s goal is not to draw conclusions about that sample but to draw conclusions about the population that the sample was selected from. Thus researchers must use sample statistics to draw conclusions about the corresponding values in the population. These corresponding values in the population are called  parameters . Imagine, for example, that a researcher measures the number of depressive symptoms exhibited by each of 50 clinically depressed adults and computes the mean number of symptoms. The researcher probably wants to use this sample statistic (the mean number of symptoms for the sample) to draw conclusions about the corresponding population parameter (the mean number of symptoms for clinically depressed adults).

Unfortunately, sample statistics are not perfect estimates of their corresponding population parameters. This is because there is a certain amount of random variability in any statistic from sample to sample. The mean number of depressive symptoms might be 8.73 in one sample of clinically depressed adults, 6.45 in a second sample, and 9.44 in a third—even though these samples are selected randomly from the same population. Similarly, the correlation (Pearson’s  r ) between two variables might be +.24 in one sample, −.04 in a second sample, and +.15 in a third—again, even though these samples are selected randomly from the same population. This random variability in a statistic from sample to sample is called  sampling error . (Note that the term error  here refers to random variability and does not imply that anyone has made a mistake. No one “commits a sampling error.”)

One implication of this is that when there is a statistical relationship in a sample, it is not always clear that there is a statistical relationship in the population. A small difference between two group means in a sample might indicate that there is a small difference between the two group means in the population. But it could also be that there is no difference between the means in the population and that the difference in the sample is just a matter of sampling error. Similarly, a Pearson’s  r  value of −.29 in a sample might mean that there is a negative relationship in the population. But it could also be that there is no relationship in the population and that the relationship in the sample is just a matter of sampling error.

In fact, any statistical relationship in a sample can be interpreted in two ways:

  • There is a relationship in the population, and the relationship in the sample reflects this.
  • There is no relationship in the population, and the relationship in the sample reflects only sampling error.

The purpose of null hypothesis testing is simply to help researchers decide between these two interpretations.

The Logic of Null Hypothesis Testing

Null hypothesis testing  is a formal approach to deciding between two interpretations of a statistical relationship in a sample. One interpretation is called the   null hypothesis  (often symbolized  H 0  and read as “H-naught”). This is the idea that there is no relationship in the population and that the relationship in the sample reflects only sampling error. Informally, the null hypothesis is that the sample relationship “occurred by chance.” The other interpretation is called the  alternative hypothesis  (often symbolized as  H 1 ). This is the idea that there is a relationship in the population and that the relationship in the sample reflects this relationship in the population.

Again, every statistical relationship in a sample can be interpreted in either of these two ways: It might have occurred by chance, or it might reflect a relationship in the population. So researchers need a way to decide between them. Although there are many specific null hypothesis testing techniques, they are all based on the same general logic. The steps are as follows:

  • Assume for the moment that the null hypothesis is true. There is no relationship between the variables in the population.
  • Determine how likely the sample relationship would be if the null hypothesis were true.
  • If the sample relationship would be extremely unlikely, then reject the null hypothesis  in favour of the alternative hypothesis. If it would not be extremely unlikely, then  retain the null hypothesis .

Following this logic, we can begin to understand why Mehl and his colleagues concluded that there is no difference in talkativeness between women and men in the population. In essence, they asked the following question: “If there were no difference in the population, how likely is it that we would find a small difference of  d  = 0.06 in our sample?” Their answer to this question was that this sample relationship would be fairly likely if the null hypothesis were true. Therefore, they retained the null hypothesis—concluding that there is no evidence of a sex difference in the population. We can also see why Kanner and his colleagues concluded that there is a correlation between hassles and symptoms in the population. They asked, “If the null hypothesis were true, how likely is it that we would find a strong correlation of +.60 in our sample?” Their answer to this question was that this sample relationship would be fairly unlikely if the null hypothesis were true. Therefore, they rejected the null hypothesis in favour of the alternative hypothesis—concluding that there is a positive correlation between these variables in the population.

A crucial step in null hypothesis testing is finding the likelihood of the sample result if the null hypothesis were true. This probability is called the  p value . A low  p  value means that the sample result would be unlikely if the null hypothesis were true and leads to the rejection of the null hypothesis. A high  p  value means that the sample result would be likely if the null hypothesis were true and leads to the retention of the null hypothesis. But how low must the  p  value be before the sample result is considered unlikely enough to reject the null hypothesis? In null hypothesis testing, this criterion is called  α (alpha)  and is almost always set to .05. If there is less than a 5% chance of a result as extreme as the sample result if the null hypothesis were true, then the null hypothesis is rejected. When this happens, the result is said to be  statistically significant . If there is greater than a 5% chance of a result as extreme as the sample result when the null hypothesis is true, then the null hypothesis is retained. This does not necessarily mean that the researcher accepts the null hypothesis as true—only that there is not currently enough evidence to conclude that it is true. Researchers often use the expression “fail to reject the null hypothesis” rather than “retain the null hypothesis,” but they never use the expression “accept the null hypothesis.”

The Misunderstood  p  Value

The  p  value is one of the most misunderstood quantities in psychological research (Cohen, 1994) [1] . Even professional researchers misinterpret it, and it is not unusual for such misinterpretations to appear in statistics textbooks!

The most common misinterpretation is that the  p  value is the probability that the null hypothesis is true—that the sample result occurred by chance. For example, a misguided researcher might say that because the  p  value is .02, there is only a 2% chance that the result is due to chance and a 98% chance that it reflects a real relationship in the population. But this is incorrect . The  p  value is really the probability of a result at least as extreme as the sample result  if  the null hypothesis  were  true. So a  p  value of .02 means that if the null hypothesis were true, a sample result this extreme would occur only 2% of the time.

You can avoid this misunderstanding by remembering that the  p  value is not the probability that any particular  hypothesis  is true or false. Instead, it is the probability of obtaining the  sample result  if the null hypothesis were true.

Role of Sample Size and Relationship Strength

Recall that null hypothesis testing involves answering the question, “If the null hypothesis were true, what is the probability of a sample result as extreme as this one?” In other words, “What is the  p  value?” It can be helpful to see that the answer to this question depends on just two considerations: the strength of the relationship and the size of the sample. Specifically, the stronger the sample relationship and the larger the sample, the less likely the result would be if the null hypothesis were true. That is, the lower the  p  value. This should make sense. Imagine a study in which a sample of 500 women is compared with a sample of 500 men in terms of some psychological characteristic, and Cohen’s  d  is a strong 0.50. If there were really no sex difference in the population, then a result this strong based on such a large sample should seem highly unlikely. Now imagine a similar study in which a sample of three women is compared with a sample of three men, and Cohen’s  d  is a weak 0.10. If there were no sex difference in the population, then a relationship this weak based on such a small sample should seem likely. And this is precisely why the null hypothesis would be rejected in the first example and retained in the second.

Of course, sometimes the result can be weak and the sample large, or the result can be strong and the sample small. In these cases, the two considerations trade off against each other so that a weak result can be statistically significant if the sample is large enough and a strong relationship can be statistically significant even if the sample is small. Table 13.1 shows roughly how relationship strength and sample size combine to determine whether a sample result is statistically significant. The columns of the table represent the three levels of relationship strength: weak, medium, and strong. The rows represent four sample sizes that can be considered small, medium, large, and extra large in the context of psychological research. Thus each cell in the table represents a combination of relationship strength and sample size. If a cell contains the word  Yes , then this combination would be statistically significant for both Cohen’s  d  and Pearson’s  r . If it contains the word  No , then it would not be statistically significant for either. There is one cell where the decision for  d  and  r  would be different and another where it might be different depending on some additional considerations, which are discussed in Section 13.2 “Some Basic Null Hypothesis Tests”

Although Table 13.1 provides only a rough guideline, it shows very clearly that weak relationships based on medium or small samples are never statistically significant and that strong relationships based on medium or larger samples are always statistically significant. If you keep this lesson in mind, you will often know whether a result is statistically significant based on the descriptive statistics alone. It is extremely useful to be able to develop this kind of intuitive judgment. One reason is that it allows you to develop expectations about how your formal null hypothesis tests are going to come out, which in turn allows you to detect problems in your analyses. For example, if your sample relationship is strong and your sample is medium, then you would expect to reject the null hypothesis. If for some reason your formal null hypothesis test indicates otherwise, then you need to double-check your computations and interpretations. A second reason is that the ability to make this kind of intuitive judgment is an indication that you understand the basic logic of this approach in addition to being able to do the computations.

Statistical Significance Versus Practical Significance

Table 13.1 illustrates another extremely important point. A statistically significant result is not necessarily a strong one. Even a very weak result can be statistically significant if it is based on a large enough sample. This is closely related to Janet Shibley Hyde’s argument about sex differences (Hyde, 2007) [2] . The differences between women and men in mathematical problem solving and leadership ability are statistically significant. But the word  significant  can cause people to interpret these differences as strong and important—perhaps even important enough to influence the college courses they take or even who they vote for. As we have seen, however, these statistically significant differences are actually quite weak—perhaps even “trivial.”

This is why it is important to distinguish between the  statistical  significance of a result and the  practical  significance of that result.  Practical significance refers to the importance or usefulness of the result in some real-world context. Many sex differences are statistically significant—and may even be interesting for purely scientific reasons—but they are not practically significant. In clinical practice, this same concept is often referred to as “clinical significance.” For example, a study on a new treatment for social phobia might show that it produces a statistically significant positive effect. Yet this effect still might not be strong enough to justify the time, effort, and other costs of putting it into practice—especially if easier and cheaper treatments that work almost as well already exist. Although statistically significant, this result would be said to lack practical or clinical significance.

Key Takeaways

  • Null hypothesis testing is a formal approach to deciding whether a statistical relationship in a sample reflects a real relationship in the population or is just due to chance.
  • The logic of null hypothesis testing involves assuming that the null hypothesis is true, finding how likely the sample result would be if this assumption were correct, and then making a decision. If the sample result would be unlikely if the null hypothesis were true, then it is rejected in favour of the alternative hypothesis. If it would not be unlikely, then the null hypothesis is retained.
  • The probability of obtaining the sample result if the null hypothesis were true (the  p  value) is based on two considerations: relationship strength and sample size. Reasonable judgments about whether a sample relationship is statistically significant can often be made by quickly considering these two factors.
  • Statistical significance is not the same as relationship strength or importance. Even weak relationships can be statistically significant if the sample size is large enough. It is important to consider relationship strength and the practical significance of a result in addition to its statistical significance.
  • Discussion: Imagine a study showing that people who eat more broccoli tend to be happier. Explain for someone who knows nothing about statistics why the researchers would conduct a null hypothesis test.
  • The correlation between two variables is  r  = −.78 based on a sample size of 137.
  • The mean score on a psychological characteristic for women is 25 ( SD  = 5) and the mean score for men is 24 ( SD  = 5). There were 12 women and 10 men in this study.
  • In a memory experiment, the mean number of items recalled by the 40 participants in Condition A was 0.50 standard deviations greater than the mean number recalled by the 40 participants in Condition B.
  • In another memory experiment, the mean scores for participants in Condition A and Condition B came out exactly the same!
  • A student finds a correlation of  r  = .04 between the number of units the students in his research methods class are taking and the students’ level of stress.

Long Descriptions

“Null Hypothesis” long description: A comic depicting a man and a woman talking in the foreground. In the background is a child working at a desk. The man says to the woman, “I can’t believe schools are still teaching kids about the null hypothesis. I remember reading a big study that conclusively disproved it years ago.” [Return to “Null Hypothesis”]

“Conditional Risk” long description: A comic depicting two hikers beside a tree during a thunderstorm. A bolt of lightning goes “crack” in the dark sky as thunder booms. One of the hikers says, “Whoa! We should get inside!” The other hiker says, “It’s okay! Lightning only kills about 45 Americans a year, so the chances of dying are only one in 7,000,000. Let’s go on!” The comic’s caption says, “The annual death rate among people who know that statistic is one in six.” [Return to “Conditional Risk”]

Media Attributions

  • Null Hypothesis by XKCD  CC BY-NC (Attribution NonCommercial)
  • Conditional Risk by XKCD  CC BY-NC (Attribution NonCommercial)
  • Cohen, J. (1994). The world is round: p < .05. American Psychologist, 49 , 997–1003. ↵
  • Hyde, J. S. (2007). New directions in the study of gender similarities and differences. Current Directions in Psychological Science, 16 , 259–263. ↵

Values in a population that correspond to variables measured in a study.

The random variability in a statistic from sample to sample.

A formal approach to deciding between two interpretations of a statistical relationship in a sample.

The idea that there is no relationship in the population and that the relationship in the sample reflects only sampling error.

The idea that there is a relationship in the population and that the relationship in the sample reflects this relationship in the population.

When the relationship found in the sample would be extremely unlikely, the idea that the relationship occurred “by chance” is rejected.

When the relationship found in the sample is likely to have occurred by chance, the null hypothesis is not rejected.

The probability that, if the null hypothesis were true, the result found in the sample would occur.

How low the p value must be before the sample result is considered unlikely in null hypothesis testing.

When there is less than a 5% chance of a result as extreme as the sample result occurring and the null hypothesis is rejected.

Research Methods in Psychology - 2nd Canadian Edition Copyright © 2015 by Paul C. Price, Rajiv Jhangiani, & I-Chant A. Chiang is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License , except where otherwise noted.

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Research Hypothesis In Psychology: Types, & Examples

Saul Mcleod, PhD

Editor-in-Chief for Simply Psychology

BSc (Hons) Psychology, MRes, PhD, University of Manchester

Saul Mcleod, PhD., is a qualified psychology teacher with over 18 years of experience in further and higher education. He has been published in peer-reviewed journals, including the Journal of Clinical Psychology.

Learn about our Editorial Process

Olivia Guy-Evans, MSc

Associate Editor for Simply Psychology

BSc (Hons) Psychology, MSc Psychology of Education

Olivia Guy-Evans is a writer and associate editor for Simply Psychology. She has previously worked in healthcare and educational sectors.

On This Page:

A research hypothesis, in its plural form “hypotheses,” is a specific, testable prediction about the anticipated results of a study, established at its outset. It is a key component of the scientific method .

Hypotheses connect theory to data and guide the research process towards expanding scientific understanding

Some key points about hypotheses:

  • A hypothesis expresses an expected pattern or relationship. It connects the variables under investigation.
  • It is stated in clear, precise terms before any data collection or analysis occurs. This makes the hypothesis testable.
  • A hypothesis must be falsifiable. It should be possible, even if unlikely in practice, to collect data that disconfirms rather than supports the hypothesis.
  • Hypotheses guide research. Scientists design studies to explicitly evaluate hypotheses about how nature works.
  • For a hypothesis to be valid, it must be testable against empirical evidence. The evidence can then confirm or disprove the testable predictions.
  • Hypotheses are informed by background knowledge and observation, but go beyond what is already known to propose an explanation of how or why something occurs.
Predictions typically arise from a thorough knowledge of the research literature, curiosity about real-world problems or implications, and integrating this to advance theory. They build on existing literature while providing new insight.

Types of Research Hypotheses

Alternative hypothesis.

The research hypothesis is often called the alternative or experimental hypothesis in experimental research.

It typically suggests a potential relationship between two key variables: the independent variable, which the researcher manipulates, and the dependent variable, which is measured based on those changes.

The alternative hypothesis states a relationship exists between the two variables being studied (one variable affects the other).

A hypothesis is a testable statement or prediction about the relationship between two or more variables. It is a key component of the scientific method. Some key points about hypotheses:

  • Important hypotheses lead to predictions that can be tested empirically. The evidence can then confirm or disprove the testable predictions.

In summary, a hypothesis is a precise, testable statement of what researchers expect to happen in a study and why. Hypotheses connect theory to data and guide the research process towards expanding scientific understanding.

An experimental hypothesis predicts what change(s) will occur in the dependent variable when the independent variable is manipulated.

It states that the results are not due to chance and are significant in supporting the theory being investigated.

The alternative hypothesis can be directional, indicating a specific direction of the effect, or non-directional, suggesting a difference without specifying its nature. It’s what researchers aim to support or demonstrate through their study.

Null Hypothesis

The null hypothesis states no relationship exists between the two variables being studied (one variable does not affect the other). There will be no changes in the dependent variable due to manipulating the independent variable.

It states results are due to chance and are not significant in supporting the idea being investigated.

The null hypothesis, positing no effect or relationship, is a foundational contrast to the research hypothesis in scientific inquiry. It establishes a baseline for statistical testing, promoting objectivity by initiating research from a neutral stance.

Many statistical methods are tailored to test the null hypothesis, determining the likelihood of observed results if no true effect exists.

This dual-hypothesis approach provides clarity, ensuring that research intentions are explicit, and fosters consistency across scientific studies, enhancing the standardization and interpretability of research outcomes.

Nondirectional Hypothesis

A non-directional hypothesis, also known as a two-tailed hypothesis, predicts that there is a difference or relationship between two variables but does not specify the direction of this relationship.

It merely indicates that a change or effect will occur without predicting which group will have higher or lower values.

For example, “There is a difference in performance between Group A and Group B” is a non-directional hypothesis.

Directional Hypothesis

A directional (one-tailed) hypothesis predicts the nature of the effect of the independent variable on the dependent variable. It predicts in which direction the change will take place. (i.e., greater, smaller, less, more)

It specifies whether one variable is greater, lesser, or different from another, rather than just indicating that there’s a difference without specifying its nature.

For example, “Exercise increases weight loss” is a directional hypothesis.

hypothesis

Falsifiability

The Falsification Principle, proposed by Karl Popper , is a way of demarcating science from non-science. It suggests that for a theory or hypothesis to be considered scientific, it must be testable and irrefutable.

Falsifiability emphasizes that scientific claims shouldn’t just be confirmable but should also have the potential to be proven wrong.

It means that there should exist some potential evidence or experiment that could prove the proposition false.

However many confirming instances exist for a theory, it only takes one counter observation to falsify it. For example, the hypothesis that “all swans are white,” can be falsified by observing a black swan.

For Popper, science should attempt to disprove a theory rather than attempt to continually provide evidence to support a research hypothesis.

Can a Hypothesis be Proven?

Hypotheses make probabilistic predictions. They state the expected outcome if a particular relationship exists. However, a study result supporting a hypothesis does not definitively prove it is true.

All studies have limitations. There may be unknown confounding factors or issues that limit the certainty of conclusions. Additional studies may yield different results.

In science, hypotheses can realistically only be supported with some degree of confidence, not proven. The process of science is to incrementally accumulate evidence for and against hypothesized relationships in an ongoing pursuit of better models and explanations that best fit the empirical data. But hypotheses remain open to revision and rejection if that is where the evidence leads.
  • Disproving a hypothesis is definitive. Solid disconfirmatory evidence will falsify a hypothesis and require altering or discarding it based on the evidence.
  • However, confirming evidence is always open to revision. Other explanations may account for the same results, and additional or contradictory evidence may emerge over time.

We can never 100% prove the alternative hypothesis. Instead, we see if we can disprove, or reject the null hypothesis.

If we reject the null hypothesis, this doesn’t mean that our alternative hypothesis is correct but does support the alternative/experimental hypothesis.

Upon analysis of the results, an alternative hypothesis can be rejected or supported, but it can never be proven to be correct. We must avoid any reference to results proving a theory as this implies 100% certainty, and there is always a chance that evidence may exist which could refute a theory.

How to Write a Hypothesis

  • Identify variables . The researcher manipulates the independent variable and the dependent variable is the measured outcome.
  • Operationalized the variables being investigated . Operationalization of a hypothesis refers to the process of making the variables physically measurable or testable, e.g. if you are about to study aggression, you might count the number of punches given by participants.
  • Decide on a direction for your prediction . If there is evidence in the literature to support a specific effect of the independent variable on the dependent variable, write a directional (one-tailed) hypothesis. If there are limited or ambiguous findings in the literature regarding the effect of the independent variable on the dependent variable, write a non-directional (two-tailed) hypothesis.
  • Make it Testable : Ensure your hypothesis can be tested through experimentation or observation. It should be possible to prove it false (principle of falsifiability).
  • Clear & concise language . A strong hypothesis is concise (typically one to two sentences long), and formulated using clear and straightforward language, ensuring it’s easily understood and testable.

Consider a hypothesis many teachers might subscribe to: students work better on Monday morning than on Friday afternoon (IV=Day, DV= Standard of work).

Now, if we decide to study this by giving the same group of students a lesson on a Monday morning and a Friday afternoon and then measuring their immediate recall of the material covered in each session, we would end up with the following:

  • The alternative hypothesis states that students will recall significantly more information on a Monday morning than on a Friday afternoon.
  • The null hypothesis states that there will be no significant difference in the amount recalled on a Monday morning compared to a Friday afternoon. Any difference will be due to chance or confounding factors.

More Examples

  • Memory : Participants exposed to classical music during study sessions will recall more items from a list than those who studied in silence.
  • Social Psychology : Individuals who frequently engage in social media use will report higher levels of perceived social isolation compared to those who use it infrequently.
  • Developmental Psychology : Children who engage in regular imaginative play have better problem-solving skills than those who don’t.
  • Clinical Psychology : Cognitive-behavioral therapy will be more effective in reducing symptoms of anxiety over a 6-month period compared to traditional talk therapy.
  • Cognitive Psychology : Individuals who multitask between various electronic devices will have shorter attention spans on focused tasks than those who single-task.
  • Health Psychology : Patients who practice mindfulness meditation will experience lower levels of chronic pain compared to those who don’t meditate.
  • Organizational Psychology : Employees in open-plan offices will report higher levels of stress than those in private offices.
  • Behavioral Psychology : Rats rewarded with food after pressing a lever will press it more frequently than rats who receive no reward.

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9.1 Null and Alternative Hypotheses

The actual test begins by considering two hypotheses . They are called the null hypothesis and the alternative hypothesis . These hypotheses contain opposing viewpoints.

H 0 : The null hypothesis: It is a statement of no difference between the variables—they are not related. This can often be considered the status quo and as a result if you cannot accept the null it requires some action.

H a : The alternative hypothesis: It is a claim about the population that is contradictory to H 0 and what we conclude when we reject H 0 . This is usually what the researcher is trying to prove.

Since the null and alternative hypotheses are contradictory, you must examine evidence to decide if you have enough evidence to reject the null hypothesis or not. The evidence is in the form of sample data.

After you have determined which hypothesis the sample supports, you make a decision. There are two options for a decision. They are "reject H 0 " if the sample information favors the alternative hypothesis or "do not reject H 0 " or "decline to reject H 0 " if the sample information is insufficient to reject the null hypothesis.

Mathematical Symbols Used in H 0 and H a :

H 0 always has a symbol with an equal in it. H a never has a symbol with an equal in it. The choice of symbol depends on the wording of the hypothesis test. However, be aware that many researchers (including one of the co-authors in research work) use = in the null hypothesis, even with > or < as the symbol in the alternative hypothesis. This practice is acceptable because we only make the decision to reject or not reject the null hypothesis.

Example 9.1

H 0 : No more than 30% of the registered voters in Santa Clara County voted in the primary election. p ≤ .30 H a : More than 30% of the registered voters in Santa Clara County voted in the primary election. p > 30

A medical trial is conducted to test whether or not a new medicine reduces cholesterol by 25%. State the null and alternative hypotheses.

Example 9.2

We want to test whether the mean GPA of students in American colleges is different from 2.0 (out of 4.0). The null and alternative hypotheses are: H 0 : μ = 2.0 H a : μ ≠ 2.0

We want to test whether the mean height of eighth graders is 66 inches. State the null and alternative hypotheses. Fill in the correct symbol (=, ≠, ≥, <, ≤, >) for the null and alternative hypotheses.

  • H 0 : μ __ 66
  • H a : μ __ 66

Example 9.3

We want to test if college students take less than five years to graduate from college, on the average. The null and alternative hypotheses are: H 0 : μ ≥ 5 H a : μ < 5

We want to test if it takes fewer than 45 minutes to teach a lesson plan. State the null and alternative hypotheses. Fill in the correct symbol ( =, ≠, ≥, <, ≤, >) for the null and alternative hypotheses.

  • H 0 : μ __ 45
  • H a : μ __ 45

Example 9.4

In an issue of U. S. News and World Report , an article on school standards stated that about half of all students in France, Germany, and Israel take advanced placement exams and a third pass. The same article stated that 6.6% of U.S. students take advanced placement exams and 4.4% pass. Test if the percentage of U.S. students who take advanced placement exams is more than 6.6%. State the null and alternative hypotheses. H 0 : p ≤ 0.066 H a : p > 0.066

On a state driver’s test, about 40% pass the test on the first try. We want to test if more than 40% pass on the first try. Fill in the correct symbol (=, ≠, ≥, <, ≤, >) for the null and alternative hypotheses.

  • H 0 : p __ 0.40
  • H a : p __ 0.40

Collaborative Exercise

Bring to class a newspaper, some news magazines, and some Internet articles . In groups, find articles from which your group can write null and alternative hypotheses. Discuss your hypotheses with the rest of the class.

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  • Authors: Barbara Illowsky, Susan Dean
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  • Book title: Introductory Statistics 2e
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Why we habitually engage in null-hypothesis significance testing: A qualitative study

Jonah stunt.

1 Department of Health Sciences, Section of Methodology and Applied Statistics, Vrije Universiteit, Amsterdam, The Netherlands

2 Department of Radiation Oncology, Erasmus Medical Center, Rotterdam, The Netherlands

Leonie van Grootel

3 Rathenau Institute, The Hague, The Netherlands

4 Department of Philosophy, Vrije Universiteit, Amsterdam, The Netherlands

5 Department of Epidemiology and Data Science, Amsterdam University Medical Centers, Amsterdam, The Netherlands

David Trafimow

6 Psychology Department, New Mexico State University, Las Cruces, New Mexico, United States of America

Trynke Hoekstra

Michiel de boer.

7 Department of General Practice and Elderly Care, University Medical Center Groningen, Groningen, The Netherlands

Associated Data

A full study protocol, including a detailed data analysis plan, was preregistered ( https://osf.io/4qg38/ ). At the start of this study, preregistration forms for qualitative studies were not developed yet. Therefore, preregistration for this study is based on an outdated form. Presently, there is a preregistration form available for qualitative studies. Information about data collection, data management, data sharing and data storage is described in a Data Management Plan. Sensitive data is stored in Darkstor, an offline archive for storing sensitive information or data (information that involves i.e., privacy or copyright). As the recordings and transcripts of the interviews and focus groups contain privacy-sensitive data, these files are archived in Darkstor and can be accessed only on request by authorized individuals (i.e., the original researcher or a research coordinator)1. Non-sensitive data is stored in DANS ( https://doi.org/10.17026/dans-2at-nzfs ) (Data Archiving and Networked Services; the Netherlands institute for permanent access to digital research resources). 1. Data requests can be send to ln.uv@mdr .

Null Hypothesis Significance Testing (NHST) is the most familiar statistical procedure for making inferences about population effects. Important problems associated with this method have been addressed and various alternatives that overcome these problems have been developed. Despite its many well-documented drawbacks, NHST remains the prevailing method for drawing conclusions from data. Reasons for this have been insufficiently investigated. Therefore, the aim of our study was to explore the perceived barriers and facilitators related to the use of NHST and alternative statistical procedures among relevant stakeholders in the scientific system.

Individual semi-structured interviews and focus groups were conducted with junior and senior researchers, lecturers in statistics, editors of scientific journals and program leaders of funding agencies. During the focus groups, important themes that emerged from the interviews were discussed. Data analysis was performed using the constant comparison method, allowing emerging (sub)themes to be fully explored. A theory substantiating the prevailing use of NHST was developed based on the main themes and subthemes we identified.

Twenty-nine interviews and six focus groups were conducted. Several interrelated facilitators and barriers associated with the use of NHST and alternative statistical procedures were identified. These factors were subsumed under three main themes: the scientific climate, scientific duty, and reactivity. As a result of the factors, most participants feel dependent in their actions upon others, have become reactive, and await action and initiatives from others. This may explain why NHST is still the standard and ubiquitously used by almost everyone involved.

Our findings demonstrate how perceived barriers to shift away from NHST set a high threshold for actual behavioral change and create a circle of interdependency between stakeholders. By taking small steps it should be possible to decrease the scientific community’s strong dependence on NHST and p-values.

Introduction

Empirical studies often start from the idea that there might be an association between a specific factor and a certain outcome within a population. This idea is referred to as the alternative hypothesis (H1). Its complement, the null hypothesis (H0), typically assumes no association or effect (although it is possible to test other effect sizes than no effect with the null hypothesis). At the stage of data-analysis, the probability of obtaining the observed, or a more extreme, association is calculated under the assumption of no effect in the population (H0) and a number of inferential assumptions [ 1 ]. The probability of obtaining the observed, or more extreme, data is known as ‘the p-value’. The p-value demonstrates the compatibility between the observed data and the expected data under the null hypothesis, where 0 is complete incompatibility and 1 is perfect compatibility [ 2 ]. When the p-value is smaller than a prespecified value (labelled as alpha, usually set at 5% (0.05)), results are generally declared to be statistically significant. At this point, researchers commonly reject the null hypothesis and accept the alternative hypothesis [ 2 ]. Assessing statistical significance by means of contrasting the data with the null hypothesis is called Null Hypothesis Significance Testing (NHST). NHST is the best known and most widely used statistical procedure for making inferences about population effects. The procedure has become the prevailing paradigm in empirical science [ 3 ], and reaching and being able to report statistically significant results has become the ultimate goal for many researchers.

Despite its widespread use, NHST and the p-value have been criticized since its inception. Numerous publications have addressed problems associated with NHST and p-values. Arguably the most important drawback is the fact that NHST is a form of indirect or inverse inference: researchers usually want to know if the null or alternative hypothesis can be accepted and use NHST to conclude either way. But with NHST, the probability of a finding, or more extreme findings, given the null hypothesis is calculated [ 4 ]. Ergo, NHST doesn’t tell us what we want to know. In fact, p-values were never meant to serve as a basis to draw conclusions, but as a continuous measure of incompatibility between empirical findings and a statistical model [ 2 ]. Moreover, the procedure promotes a dichotomous way of thinking, by using the outcome of a significance test as a dichotomous indicator for an effect (p<0.05: effect, p>0.05: no effect). Reducing empirical findings to two categories also results in a great loss of information. Further, a significant outcome is often unjustly interpreted as relevant, but a p-value does not convey any information about the strength or importance of the association. Worse yet, the p-values on which NHST is based confound effect size and sample size. A trivial effect size may nevertheless result in statistical significance provided a sufficiently large sample size. Or an important effect size may fail to result in statistical significance if the sample size is too small. P-values do not validly index the size, relevance, or precision of an effect [ 5 ]. Furthermore, statistical models include not only null hypotheses, but additional assumptions, some of which are wrong, such as the ubiquitous assumption of random and independent sampling from a defined population [ 1 ]. Therefore, although p-values validly index the incompatibility of data with models, p-values do not validly index incompatibility of data with hypotheses that are embedded in wrong models. These are important drawbacks rendering NHST unsuitable as the default procedure for drawing conclusions from empirical data [ 2 , 3 , 5 – 13 ].

A number of alternatives have been developed that overcome these pitfalls, such as Bayesian inference methods [ 7 , 11 , 14 , 15 ], informative hypothesis testing [ 9 , 16 ] and a priori inferential statistics [ 4 , 17 ]. These alternatives build on the idea that research usually starts with a more informed research-question than one merely assuming the null hypothesis of no effect. These methods overcome the problem of inverse inference, although the first two might still lead to dichotomous thinking with the use of thresholds. Despite the availability of alternatives, statistical behavior in the research community has hardly changed. Researchers have been slow to adopt alternative methods and NHST is still the prevailing paradigm for making inferences about population effects [ 3 ].

Until now, reasons for the continuous and ubiquitous use of NHST and the p-value have scarcely been investigated. One explanation is that NHST provides a very simple means for drawing conclusions from empirical data, usually based on the 5% cut-off. Secondly, most researchers are unaware of the pitfalls of NHST; it has been shown that NHST and the p-value are often misunderstood and misinterpreted [ 2 , 3 , 8 , 11 , 18 , 19 ]. Thirdly, NHST has a central role in most methods and statistics courses in higher education. Courses on alternative methods are increasingly being offered but are usually not mandatory. To our knowledge, there is a lack of in depth, empirical research, aimed at elucidating why NHST nevertheless remains the dominant approach, or what actions can be taken to shift the sciences away from NHST. Therefore, the aim of our study was to explore the perceived barriers and facilitators, as well as behavioral intentions related to the use of NHST and alternatives statistical procedures, among all relevant stakeholders in the scientific system.

Theoretical framework

In designing our study, we used two theories. Firstly, we used the ‘diffusion of innovation theory’ of Rogers [ 20 ]. This theory describes the dissemination of an innovation as a process consisting of four elements: 1) an innovation is 2) communicated through certain channels 3) over time 4) among the members of a social system [ 20 ]. In the current study, the innovation consists of the idea that we should stop with the default use of NHST and instead consider using alternative methods for drawing conclusions from empirical data. The science system forms the social structure in which the innovation should take place. The most important members, and potential adopters of the innovation, we identified are researchers, lecturers, editors of scientific journals and representatives of funding agencies. Rogers describes phases in the adoption process, which coincide with characteristics of the (potential) adopters of the idea: 1) innovators, 2) early adopters, 3) early majority adopters, 4) late majority adopters and 5) laggards. Innovators are the first to adopt an innovation. There are few innovators but these few are very important for bringing in new ideas. Early adopters form the second group to adopt an innovation. This group includes opinion leaders and role models for other stakeholders. The largest group consists of the early and late majority who follow the early adopters, and then there is a smaller group of laggards who resist the innovation until they are certain the innovation will not fail. The process of innovation adoption by individuals is described as a normal distribution ( Fig 1 ). For these five groups, the adoption of a new idea is influenced by the following five characteristics of the innovative idea and 1) its relative advantage, 2) its compatibility with current experiences, 3) its complexity, 4) its flexibility, and 5) its visibility [ 20 ]. Members of all four stakeholder groups could play an important role in the diffusion of the innovation of replacing NHST by its alternatives.

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The innovativeness dimension, measured by the time at which an individual from an adopter category adopts an innovation. Each category is one of more standard deviations removed from the average time of adoption [ 20 ].

Another important theory for our study is the ‘theory of planned behavior’, that was developed in the 1960s [ 21 ]. This theory describes how human behavior in a certain context can be predicted and explained. The theory was updated in 2010, under the name ‘the reasoned action approach’ [ 22 ]. A central factor in this theory is the intention to perform a certain behavior, in this case, to change the default use of NHST. According to the theory, people’s intentions determine their behaviors. An intention indexes to what extent someone is motivated to perform the behavior. Intentions are determined by three independent determinants: the person’s attitudes toward the behavior—the degree to which a person sees the behavior as favorable or unfavorable, perceived subjective norms regarding the behavior—the perceived social pressure to perform the behavior or not, and perceptions of control regarding the behavior—the perceived ease or difficulty of performing the behavior. Underlying (i.e. responsible for) these three constructs are corresponding behavioral, normative, and control beliefs [ 21 , 22 ] (see Fig 2 ).

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Both theories have served as a lens for both data collection and analysis. We used sensitizing concepts [ 23 ] within the framework of the grounded theory approach [ 24 ] from both theories as a starting point for this qualitative study, and more specifically, for the topic list for the interviews and focus groups, providing direction and guidance for the data collection and data analysis.

Many of the concepts of Rogers’ and Fishbein and Ajzen’s theory can be seen as facilitators and barriers for embracing and implementing innovation in the scientific system.

A qualitative study among stakeholders using semi-structured interviews and focus groups was performed. Data collection and analysis were guided by the principle of constant comparison traditional to the grounded theory approach we followed [ 24 ]. The grounded theory is a methodology that uses inductive reasoning, and aims to construct a theory through the collection and analysis of data. Constant comparison is the iterative process whereby each part of the data that emerges from the data analysis is compared with other parts of the data to thoroughly explore and validate the data. Concepts that have been extracted from the data are tagged with codes that are grouped into categories. These categories constitute themes, which (may) become the basis for a new theory. Data collection and analysis were continued until no new information was gained and data saturation had likely occurred within the identified themes.

The target population consisted of stakeholders relevant to our topic: junior and senior researchers, lecturers in statistics, editors of scientific journals and program leaders of funding agencies (see Tables ​ Tables1 1 and ​ and2). 2 ). We approached participants in the field of medical sciences, health- and life sciences and psychology. In line with the grounded theory approach, theoretical sampling was used to identify and recruit eligible participants. Theoretical sampling is a form of purposive sampling. This means that we aimed to purposefully select participants, based on their characteristics that fit the parameters of the research questions [ 25 ]. Recruitment took place by approaching persons in our professional networks and or the networks of the approached persons.

*The numbers between brackets represents the number of participants that were also interviewed.

Data collection

We conducted individual semi-structured interviews followed by focus groups. The aim of the interviews was to gain insight into the views of participants on the use of NHST and alternative methods and to examine potential barriers and facilitators related to these methods. The aim of the focus groups was to validate and further explore interview findings and to develop a comprehensive understanding of participants’ views and beliefs.

For the semi-structured interviews, we used a topic list (see Appendix 1 in S1 Appendix ). Questions addressed participants’ knowledge and beliefs about the concept of NHST, their familiarity with NHST, perceived attractiveness and drawbacks of the use of NHST, knowledge of the current NHST debate, knowledge of and views on alternative procedures and their views on the future of NHST. The topic list was slightly adjusted based on the interviews with editors and representatives from funding agencies (compared to the topic list for interviews with researchers and lecturers). Questions particularly focused on research and education were replaced by questions focused on policy (see Appendix 1 in S1 Appendix ).

The interviews were conducted between October 2017 and June 2018 by two researchers (L.v.G. and J.S.), both trained in qualitative research methods. Interviews lasted about one hour (range 31–86 minutes) and were voice-recorded. One interview was conducted by telephone; all others were face to face and took place at a location convenient for the participants, in most cases the participants’ work location.

Focus groups

During the focus groups, important themes that emerged from the interviews were discussed and explored. These include perceptions on NHST and alternatives and essential conditions to shift away from the default use of NHST.

Five focus groups included representatives from the different stakeholder groups. One focus group was homogenous, including solely lecturers. The focus groups consisted of ‘old’ as well as ‘new’ participants, that is, some of the participants of the focus groups were also in the interview sample. We also selected persons that were open for further contribution to the NHST debate and were willing to help think about (implementing) alternatives for NHST.

The focus groups were conducted between September and December 2018 by three researchers (L.v.G., J.S. and A.d.K.), all trained in qualitative research methods. The focus groups lasted about one-and-a-half hours (range 86–100 minutes).

Data analysis

All interviews and focus groups were transcribed verbatim. Atlas.ti 8.0 software was used for data management and analysis. All transcripts were read thoroughly several times to identify meaningful and relevant text fragments and analyzed by two researchers (J.S. and L.v.G.). Deductive predefined themes and theoretical concepts were used to guide the development of the topic list for the semi-structured interviews and focus groups, and were used as sensitizing concepts [ 23 ] in data collection and data analysis. Inductive themes were identified during the interview process and analysis of the data [ 26 ].

Transcripts were open-, axial- and selectively coded by two researchers (J.S. and L.v.G.). Open coding is the first step in the data-analysis, whereby phenomena found in the text are identified and named (coded). With axial coding, connections between codes are drawn. Selective coding is the process of selecting one central category and relating all other categories to that category, capturing the essence of the research. The constant comparison method [ 27 ] was applied allowing emerging (sub)themes to be fully explored. First, the two researchers independently developed a set of initial codes. Subsequently, findings were discussed until consensus was reached. Codes were then grouped into categories that were covered under subthemes, belonging to main themes. Finally, a theory substantiating the prevailing use of NHST was developed based on the main themes and subthemes.

Ethical issues

This research was conducted in accordance with the Dutch "General Data Protection Regulation" and the “Netherland’s code of conduct for research integrity”. The research protocol had been submitted for review and approved by the ethical review committee of the VU Faculty of Behavioral and Movement Sciences. In addition, the project had been submitted to the Medical Ethics Committee (METC) of the Amsterdam University Medical Centre who decided that the project is not subject to the Medical Research (Human Subjects) Act ( WMO). At the start of data collection, all participants signed an informed consent form.

A full study protocol, including a detailed data analysis plan, was preregistered ( https://osf.io/4qg38/ ). At the start of this study, preregistration forms for qualitative studies were not developed yet. Therefore, preregistration for this study is based on an outdated form. Presently, there is a preregistration form available for qualitative studies [ 28 ]. Information about data collection, data management, data sharing and data storage is described in a Data Management Plan. Sensitive data is stored in Darkstor, an offline archive for storing sensitive information or data (information that involves i.e., privacy or copyright). As the recordings and transcripts of the interviews and focus groups contain privacy-sensitive data, these files are archived in Darkstor and can be accessed only on request by authorized individuals (i.e., the original researcher or a research coordinator) (Data requests can be send to ln.uv@mdr ). Non-sensitive data is stored in DANS ( https://doi.org/10.17026/dans-2at-nzfs ) (Data Archiving and Networked Services; the Netherlands institute for permanent access to digital research resources).

Participant characteristics

Twenty-nine individual interviews and six focus groups were conducted. The focus groups included four to six participants per session. A total of 47 participants were included in the study (13 researchers, 15 lecturers, 11 editors of scientific journals and 8 representatives of funding agencies). Twenty-nine participants were interviewed. Twenty-seven participants took part in the focus group. Nine of the twenty-seven participants were both interviewed and took part in the focus groups. Some participants had multiple roles (i.e., editor and researcher, editor and lecturer or lecturer and researcher) but were classified based on their primary role (assistant professors were classified as lecturers). The lecturers in statistics in our sample were not statisticians themselves. Although they all received training in statistics, they were primarily trained as psychologists, medical doctors, or health scientists. Some lecturers in our sample taught an applied subject, with statistics as part of it. Other lectures taught Methodology and Statistics courses. Statistical skills and knowledge among lecturers varied from modest to quite advanced. Statistical skills and knowledge among participants from the other stakeholder groups varied from poor to quite advanced. All participants were working in the Netherlands. A general overview of the participants is presented in Table 1 . Participant characteristics split up by interviews and focus groups are presented in Table 2 .

Three main themes with sub-themes and categories emerged ( Fig 3 ): the green-colored compartments hold the three main themes: The scientific climate , The scientific duty and Reactivity . Each of these three main themes consists of subthemes, depicted by the yellow-colored compartments. In turn, some (but not all) of the 9 subthemes also have categories. These ‘lower level’ findings are not included in the figure but will be mentioned in the elaboration on the findings and are depicted in Appendix 2 in S1 Appendix . Fig 3 shows how the themes are related to each other. The blue arrows indicate that the themes are interrelated; factors influence each other. The scientific climate affects the way stakeholders perceive and fulfil their scientific duty, the way stakeholders give substance to their scientific duty shapes and maintain the scientific climate. The scientific duty and the scientific climate cause a state of reactivity. Many participants have adopted a ’wait and see’ attitude regarding behavioral changes with respect to statistical methods. They feel dependent on someone else’s action. This leads to a reactive (instead of a proactive) attitude and a low sense of responsibility. ‘Reactivity’ is the core theme, explaining the most critical problem with respect to the continuous and ubiquitous use of NHST.

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Main themes and subthemes are numbered. Categories are mentioned in the body of the text in bold. ‘P’ stands for participant; ‘I’ stands for interviewer.

1. The scientific climate

The theme, ‘the scientific climate’, represents researchers’ (Dutch) perceptions of the many written and unwritten rules they face in the research environment. This theme concerns the opportunities and challenges participants encounter when working in the science system. Dutch academics feel pressured to publish fast and regularly, and to follow conventions and directions of those on whom they depend. They feel this comes at the expense of the quality of their work. Thus, the scientific climate in the Netherlands has a strong influence on the behavior of participants regarding how they set their priorities and control the quality of their work.

1 . 1 Quality control . Monitoring the quality of research is considered very important. Researchers, funding agencies and editors indicate they rely on their own knowledge, expertise, and insight, and those of their colleagues, to guarantee this quality. However, editors or funding agencies are often left with little choice when it comes to compiling an evaluation committee or a review panel. The choice is often like-knows-like-based. Given the limited choice, they are forced to trust the opinion of their consultants, but the question is whether this is justified.

I: “The ones who evaluate the statistics, do they have sufficient statistical knowledge?” P: “Ehhr, no, I don’t think so.” I: “Okay, interesting. So, there are manuscripts published of which you afterwards might think….” P: “Yes yes.” (Interview 18; Professor/editor, Medical Sciences)

1 . 2 Convention . The scientific system is built on mores and conventions, as this participant describes:

P: “There is science, and there is the sociology of science, that is, how we talk to each other, what we believe, how we connect. And at some point, it was agreed upon that we would talk to each other in this way.” (Interview 28, researcher, Medical Sciences)

And to these conventions, one (naturally) conforms. Stakeholders copy behavior and actions of others within their discipline, thereby causing particular behaviors and values to become conventional or normative. One of those conventions is the use of NHST and p-values. Everyone is trained with NHST and is used to applying this method. Another convention is the fact that significant results mean ‘success’, in the sense of successful research and being a successful researcher. Everyone is aware that ‘p is smaller than 0.05’ means the desired results are achieved and that publication and citation chances are increased.

P: “You want to find a significant result so badly. (…) Because people constantly think: I must find a significant result, otherwise my study is worthless.” (Focus group 4, lecturer, Medical Sciences)

Stakeholders rigidly hold on to the above-mentioned conventions and are not inclined to deviate from existing norms; they are, in other words, quite conservative . ‘We don’t know any better’ has been brought up as a valid argument by participants from various stakeholder groups to stick to current rules and conventions. Consequently, the status quo in the scientific system is being maintained.

P: “People hold on to….” I: ‘Everyone maintains the system?’ P: ‘Yes, we kind of hang to the conservative manner. This is what we know, what someone, everyone, accepts.” (Interview 17, researcher, Health Sciences)

Everyone is trained with NHST and considers it an accessible and easy to interpret method. The familiarity and perceived simplicity of NHST, user-friendly software such as SPSS and the clear cut-off value for significance are important facilitators for the use of NHST and at the same time barriers to start using alternative methods. Applied researchers stressed the importance of the accessibility of NHST as a method to test hypotheses and draw conclusions. This accessibility also justifies the use of NHST when researchers want to communicate their study results and messages in understandable ways to their readership.

P: “It is harder, also to explain, to use an alternative. So, I think, but maybe I’m overstepping, but if you want to go in that direction [alternative methods] it needs to be better facilitated for researchers. Because at the moment… I did some research, but, you know, there are those uncommon statistical packages.” (Interview 16, researcher/editor, Medical Sciences)

1 . 3 Publication pressure . Most researchers mentioned that they perceive publication pressure. This motivates them to use NHST and hope for significant results, as ‘significant p-values’ increase publication chances. They perceive a high workload and the way the scientific reward system is constructed as barriers for behavioral change pertaining to the use of statistical methods; potential negative consequences for publication and career chances prevent researchers from deviating from (un)written rules.

P: “I would like to learn it [alternative methods], but it might very well be that I will not be able to apply it, because I will not get my paper published. I find that quite tricky.” (Interview 1, Assistant Professor, Health Sciences)

2. The scientific duty

Throughout the interviews, participants reported a sense of duty in several variations. “What does it mean to be a scientific researcher?” seemed to be a question that was reflected upon during rather than prior to the interview, suggesting that many scientists had not really thought about the moral and professional obligations of being a scientist in general—let alone what that would mean for their use of NHST. Once they had given it some thought, the opinions concerning what constitutes the scientific duty varied to a large extent. Some participants attached great importance to issues such as reproducibility and transparency in scientific research and continuing education and training for researchers. For others, these topics seemed to play a less important role. A distinction was made between moral and professional obligations that participants described concerning their scientific duty.

2 . 1 Moral obligation . The moral obligation concerns issues such as doing research in a thorough and honest way, refraining from questionable research practices (QRPs) and investing in better research. It concerns tasks and activities that are not often rewarded or acknowledged.

Throughout the interviews and the focus groups, participants very frequently touched upon the responsibility they felt for doing ‘the right thing’ and making the right choice in doing research and using NHST, in particular. The extent to which they felt responsible varied among participants. When it comes to choices during doing research—for example, drawing conclusions from data—participants felt a strong sense of responsibility to do this correctly. However, when it comes to innovation and new practices, and feeling responsible for your own research, let alone improving scientific practice in general, opinions differed. This quotation from one of the focus groups illustrates that:

P1: “If you people [statisticians, methodologists] want me to improve the statistics I use in my research, then you have to hand it to me. I am not going to make any effort to improve that myself. “P3: “No. It is your responsibility as an academic to keep growing and learning and so, also to start familiarizing yourself when you notice that your statistics might need improvement.” (Focus group 2, participant 1 (PhD researcher, Medical Sciences) and 3 (Associate Professor, Health Sciences)

The sense of responsibility for improving research practices regarding the use of NHST was strongly felt and emphasized by a small group of participants. They emphasized the responsibility of the researcher to think, interpret and be critical when interpreting the p -value in NHST. It was felt that you cannot leave that up to the reader. Moreover, scrutinizing and reflecting upon research results was considered a primary responsibility of a scientist, and failing to do so, as not living up to what your job demands you to do:

P: “Yes, and if I want to be very provocative—and I often want that, because then people tend to wake up and react: then I say that hiding behind alpha.05 is just scientific laziness. Actually, it is worse: it is scientific cowardice. I would even say it is ‘relieving yourself from your duty’, but that may sound a bit harsh…” (Interview 2, Professor, Health Sciences)

These participants were convinced that scientists have a duty to keep scientific practice in general at the highest level possible.

The avoidance of questionable research practices (QRPs) was considered a means or a way to keep scientific practices high level and was often touched upon during the interviews and focus groups as being part of the scientific duty. Statisticians saw NHST as directly facilitating QRPs and providing ample examples of how the use of NHST leads to QRPs, whereas most applied researchers perceived NHST as the common way of doing research and were not aware of the risks related to QRPs. Participants did mention the violation of assumptions underlying NHST as being a QRP. Then, too, participants considered overinterpreting results as a QRP, including exaggerating the degree of significance. Although participants stated they were careful about interpreting and reporting p-values, they ‘admitted’ that statistical significance was a starting point for them. Most researchers indicated they search for information that could get their study published, which usually includes a low p-value (this also relates to the theme ‘Scientific climate’).

P: “We all know that a lot of weight is given to the p-value. So, if it is not significant, then that’s the end of it. If it ís significant, it just begins.” (Interview 5, lecturer, Psychology)

The term ‘sloppy science’ was mentioned in relation to efforts by researchers to reduce the p -value (a.k.a. p-hacking, data-dredging, and HARKing. HARKing is an acronym that refers to the questionable research question of Hypothesizing After the Results are Known. It occurs when researchers formulate a hypothesis after the data have been collected and analyzed, but make it look like it is an a priori hypothesis [ 29 ]). Preregistration and replication were mentioned as being promising solutions for some of the problems caused by NHST.

2 . 2 . Professional obligation . The theme professional obligation reflects participants’ expressions about what methodological knowledge scientists should have about NHST. In contrast moral obligations, there appeared to be some consensus about scientists’ professional obligations. Participants considered critical evaluation of research results a core professional obligation. Also, within all the stakeholder groups, participants agreed that sufficient statistical knowledge is required for using NHST, but they varied in their insights in the principles, potential and limitations of NHST. This also applied to the extent to which participants were aware of the current debate about NHST.

Participants considered critical thinking as a requirement for fulfilling their professional obligation. It specifically refers to the process of interpreting outcomes and taking all relevant contextual information into consideration. Critical thinking was not only literally referred to by participants, but also emerged by interpreting text fragments on the emphasis within their research. Researchers differed quite strongly in where the emphasis of their research outcomes should be put and what kind of information is required when reporting study results. Participants mentioned the proven effectiveness of a particular treatment, giving a summary of the research results, effect sizes, clinical relevance, p-values, or whether you have made a considerable contribution to science or society.

P: “I come back to the point where I said that people find it arbitrary to state that two points difference on a particular scale is relevant. They prefer to hide behind an alpha of 0.05, as if it is a God given truth, that it counts for one and for all. But it is just as well an invented concept and an invented guideline, an invented cut-off value, that isn’t more objective than other methods?” (Interview 2, Professor, Health Sciences)

For some participants, especially those representing funding agencies, critical thinking was primarily seen as a prerequisite for the utility of the research. The focus, when formulating the research question and interpreting the results, should be on practical relevance and the contribution the research makes to society.

The term ‘ignorance’ arose in the context of the participants’ concern regarding the level of statistical knowledge scientists and other stakeholders have versus what knowledge they should have to adequately apply statistical analysis in their research. The more statistically competent respondents in the sample felt quite strongly about how problematic the lack of knowledge about NHST is among those who regularly use it in their research, let alone the lack of knowledge about alternative methods. They felt that regularly retraining yourself in research methods is an essential part of the professional obligation one has. Applied researchers in the sample agreed that a certain level of background knowledge on NHST was required to apply it properly to research and acknowledged their own ignorance. However, they had different opinions about what level of knowledge is required. Moreover, not all of them regarded it as part of their scientific duty to be informed about all ins and outs of NHST. Some saw it as the responsibility of statisticians to actively inform them (see also the subtheme periphery). Some participants were not aware of their ignorance or stated that some of their colleagues are not aware of their ignorance, i.e., that they are unconsciously incompetent and without realizing it, poorly understood what the p-value and associated outcome measures actually mean.

P: “The worst, and I honestly think that this is the most common, is unconsciously incompetent, people don’t even understand that…” I: “Ignorance.” P: “Yes, but worse, ignorant and not even knowing you are ignorant.” (Interview 2, Professor, Health Sciences)

The lack of proper knowledge about statistical procedures was especially prevalent in the medical sciences. Participants working in or with the medical sciences all confirmed that there is little room for proper statistical training for medical students and that the level of knowledge is fairly low. NHST is often used because of its simplicity. It is especially attractive for medical PhD students because they need their PhD to get ahead in their medical career instead of pursuing a scientific career.

P: “I am not familiar with other ways of doing research. I would really like to learn, but I do not know where I could go. And I do not know whether there are better ways. So sometimes I do read studies of which I think: ‘this is something I could investigate with a completely different test. Apparently, this is also possible, but I don’t know how.’ Yes, there are courses, but I do not know what they are. And here in the medical center, a lot of research is done by medical doctors and these people have hardly been taught any statistics. Maybe they will get one or two statistics courses, they know how to do a t-test and that is about it. (…) And the courses have a very low level of statistics, so to say.” (Interview 1, Assistant Professor, Health Sciences)

Also, the term ‘ awareness ’ arose. Firstly, it refers to being conscious about the limitations of NHST. Secondly, it refers to the awareness of the ongoing discussions about NHST and more broadly, about the replication crisis. The statisticians in the sample emphasized the importance of knowing that NHST has limitations and that it cannot be considered the holy grail of data analysis. They also emphasized the importance of being aware of the debate. A certain level of awareness was considered a necessary requirement for critical thinking. There was variation in that awareness. Some participants were quite informed and were also fairly engaged in the discussion whereas others were very new to the discussion and larger contextual factors, such as the replication crisis.

I: “Are you aware of the debate going on in academia on this topic [NHST]? P: “No, I occasionally see some article sent by a colleague passing by. I have the idea that something is going on, but I do not know how the debate is conducted and how advanced it is. (Interview 6, lecturer, Psychology)

With respect to the theme, ‘the scientific duty’, participants differed to what extent they felt responsible for better and open science, for pioneering, for reviewing, and for growing and learning as a scientist. Participants had one commonality: although they strived for adherence to the norms of good research, the rampant feeling is that this is very difficult, due to the scientific climate. Consequently, participants perceive an internal conflict : a discrepancy between what they want or believe , and what they do . Participants often found themselves struggling with the responsibility they felt they had. Making the scientifically most solid choice was often difficult due to feasibility, time constraints, or certain expectations from supervisors (this is also directly related to the themes ‘Scientific climate’ and ‘Reactivity’). Thus, the scientific climate strongly influences the behavior of scientists regarding how they set their priorities and fulfill their scientific duties. The strong sense of scientific duty was perceived by some participants as a facilitator and by others as a barrier for the use of alternative methods.

3. Reactivity

A consequence of the foregoing factors is that most stakeholders have adopted a reactive attitude and behave accordingly. People are disinclined to take responsibility and await external signals and initiatives of others. This might explain why NHST is being continuously used and remains the default procedure to make inferences about population effects.

The core theme ‘reactivity’ can be explained by the following subthemes and categories:

3 . 1 Periphery . The NHST-problem resides in the periphery in several ways. First, it is a subject that is not given much priority. Secondly, some applied researchers and editors believe that methodological knowledge, as it is not their field of expertise, should not be part of their job requirement. This also applies to the NHST debate. Thirdly, and partly related to the second point, there is a lack of cooperation within and between disciplines.

The term ‘ priority’ was mentioned often when participants were asked to what extent the topic of NHST was subject of discussion in their working environment. Participants indicated that (too) little priority is given to statistics and the problems related to the subject. There is simply a lot going on in their research field and daily work, so there are always more important or urgent issues on the agenda.

P: “Discussions take place in the periphery; many people find it complicated. Or are just a little too busy.” (Interview 5, lecturer, Psychology)

As the NHST debate is not prioritized, initiatives with respect to this issue are not forthcoming. Moreover, researchers and lecturers claim there is neither time nor money available for training in statistics in general or acquiring more insight and skills with respect to (the use of) alternative methods. Busy working schedules were mentioned as an important barrier for improving statistical knowledge and skills.

P: “Well you can use your time once, so it is an issue low on the priority list.” (Focus group 5, researcher, Medical Sciences)

The NHST debate is perceived as the domain of statisticians and methodologists. Also, cooperation between different domains and domain-specific experts is perceived as complicated, as different perceptions and ways of thinking can clash. Therefore, some participants feel that separate worlds should be kept separate; put another way: stick to what you know!

P: “This part is not our job. The editorial staff, we have the assignment to ensure that it is properly written down. But the discussion about that [alternatives], that is outside our territory.” (Interview 26, editor, Medical Sciences)

Within disciplines, individuals tend to act on their own, not being aware that others are working on the same subject and that it would be worthwhile to join forces. The interviews and focus groups exposed that a modest number of participants actively try to change the current situation, but in doing that, feel like lone voices in the wilderness.

P1: “I mean, you become a lone voice in the wilderness.” P2: “Indeed, you don’t want that.” P1: “I get it, but no one listens. There is no audience.” (Focus Group 3, P1: MD, lecturer, medical Sciences, P2: editor, Medical Sciences)

To succeed at positive change, participants emphasized that it is essential that people (interdisciplinary) cooperate and join forces, rather than operate on individual levels, focusing solely on their own working environment.

The caution people show with respect to taking initiative is reenforced by the fear of encountering resistance from their working environment when one voices that change regarding the use of NHST is needed. A condition that was mentioned as essential to bring about change was tactical implementation , that is, taking very small steps. As everyone is still using NHST, taking big steps brings the risk of losing especially the more conservative people along the way. Also, the adjustment of policy, guidelines and educational programs are processes for which we need to provide time and scope.

P: “Everyone still uses it, so I think we have to be more critical, and I think we have to look at some kind of culture change, that means that we are going to let go of it (NHST) more and we will also use other tests, that in the long term will overthrow NHST. I: and what about alternatives? P: I think you should never be too fanatic in those discussion, because then you will provoke resistance. (…) That is not how it works in communication. You will touch them on a sore spot, and they will think: ‘and who are you?’ I: “and what works?” P: “well, gradualness. Tell them to use NHST, do not burn it to the ground, you do not want to touch peoples work, because it is close to their hearts. Instead, you say: ‘try to do another test next to NHST’. Be a pioneer yourself.” (Interview 5, lecturer, Psychology)

3 . 2 . Efficacy . Most participants stated they feel they are not in the position to initiate change. On the one hand, this feeling is related to their hierarchical positions within their working environments. On the other hand, the feeling is caused by the fact that statistics is perceived as a very complex field of expertise and people feel they lack sufficient knowledge and skills, especially about alternative methods.

Many participants stated they felt little sense of empowerment, or self-efficacy. The academic system is perceived as hierarchical, having an unequal balance of power. Most participants believe that it is not in their power to take a lead in innovative actions or to stand up against establishment, and think that this responsibility lies with other stakeholders, that have more status .

P: “Ideally, there would be a kind of an emergency letter from several people whose names open up doors, in which they indicate that in the medical sciences we are throwing away money because research is not being interpreted properly. Well, if these people that we listen to send such an emergency letter to the board of The Netherlands Organization for Health Research and Development [the largest Dutch funding agency for innovation and research in healthcare], I can imagine that this will initiate a discussion.” (…) I: “and with a big name you mean someone from within the science system? P: well, you know, ideally a chairman, or chairmen of the academic medical center. At that level. If they would put a letter together. Yes, that of course would have way more impact. Or some prominent medical doctors, yes, that would have more impact, than if some other person would send a letter yes.” (Interview 19, representative from funding agency, Physical Sciences)

Some participants indicated that they did try to make a difference but encountered too much resistance and therefore gave up their efforts. PhD students feel they have insufficient power to choose their own directions and make their own choices.

P: I am dependent on funding agencies and professors. In the end, I will write a grant application in that direction that gives me the greatest chance of eventually receiving that grant. Not primarily research that I think is the most optimal (…) If I know that reviewers believe the p-value is very important, well, of course I write down a method in which the p-value is central.” (Focus group 2, PhD-student, Medical Sciences)

With a sense of imperturbability, most participants accept that they cannot really change anything.

Lastly, the complexity of the subject is an obstacle for behavioral change. Statistics is perceived as a difficult subject. Participants indicate that they have a lack of knowledge and skills and that they are unsure about their own abilities. This applies to the ‘standard’ statistical methods (NHST), but to a greater extent to alternative methods. Many participants feel that they do not have the capacity to pursue a true understanding of (alternative) statistical methods.

P: “Statistics is just very hard. Time and again, research demonstrates that scientists, even the smartest, have a hard time with statistics.” (Focus group 3, PhD researcher, Psychology)

3 . 3 . Interdependency . As mentioned, participants feel they are not in a sufficiently strong position to take initiative or to behave in an anti-establishment manner. Therefore, they await external signals from people within the scientific system with more status, power, or knowledge. This can be people within their own stakeholder group, or from other stakeholder groups. As a consequence of this attitude, a situation arises in which peoples’ actions largely depend on others. That is, a complex state of interdependency evolves: scientists argue that if the reward system does not change, they are not able to alter their statistical behavior. According to researchers, editors and funding agencies are still very much focused on NHST and especially (significant) p-values, and thus, scientists wait for editors and funders to adjust their policy regarding statistics:

P: “I wrote an article and submitted it to an internal medicine journal. I only mentioned confidence intervals. Then I was asked to also write down the p-values. So, I had to do that. This is how they [editors] can use their power. They decide.” (Interview 1, Assistant Professor, Health Sciences)

Editors and funders in their turn claim they do not maintain a strict policy. Their main position is that scientists should reach consensus about the best statistical procedure, and they will then adjust their policy and guidelines.

P: “We actually believe that the research field itself should direct the quality of its research, and thus, also the discussions.” (Interview 22, representative from funding agency, Neurosciences)

Lecturers, for their part, argue that they cannot revise their educational programs due to the academic system, and university policies are adapted to NHST and p-values.

As most participants seem not to be aware of this process, a circle of interdependency arises that is difficult to break.

P: “Yes, the stupid thing about this perpetual circle is that you are educating people, let’s say in the department of cardiology. They must of course grow, and so they need to publish. If you want to publish you must meet the norms and values of the cardiology journals, so they will write down all those p-values. These people are trained and in twenty years they are on the editorial board of those journals, and then you never get rid of it [the p-value].” (Interview 18, Professor, editor, Medical Sciences)

3 . 4 . Degree of eagerness . Exerting certain behavior or behavioral change is (partly) determined by the extent to which people want to employ particular behavior, their behavioral intention [ 22 ]. Some participants indicated they are willing to change their behavior regarding the use of statistical methods, but only if it is absolutely necessary, imposed or if they think that the current conventions have too many negative consequences. Thus, true, intrinsic will-power to change behavior is lacking among these participants. Instead, they have a rather opportunistic attitude, meaning that their behavior is mostly driven by circumstances, not by principles.

P: “If tomorrow an alternative is offered by people that make that call, than I will move along. But I am not the one calling the shots on this issue.” (Interview 26, editor, Medical Sciences)

In addition, pragmatism often outweighs the perceived urgency to change. Participants argue they ‘just want to do their jobs’ and consider the practical consequences mainly in their actions. This attitude creates a certain degree of inertia. Although participants claim they are willing to change their behavior, this would contain much more than ‘doing their jobs, and thus, in the end, the NHST-debate is subject to ‘coffee talk’. People are open to discussion, but when it comes to taking action (and motivating others to do so), no one takes action.

P: “The endless analysis of your data to get something with a p-value less than 0.05… There are people that are more critical about that, and there are people that are less critical. But that is a subject for during the coffee break.” (Interview 18, professor, editor, Medical Sciences)

The goal of our study was to acquire in-depth insight into reasons why so many stakeholders from the scientific system keep using NHST as the default method to draw conclusions, despite its many well-documented drawbacks. Furthermore, we wanted to gain insight into the reasons for their reluctance to apply alternative methods. Using a theoretical framework [ 20 , 21 ], several interrelated facilitators and barriers associated with the use of NHST and alternative methods were identified. The identified factors are subsumed under three main themes: the scientific climate, the scientific duty and reactivity. The scientific climate is dominated by conventions, behavioral rules, and beliefs, of which the use of NHST and p-values is part. At the same time, stakeholders feel they have a (moral or professional) duty. For many participants, these two sides of the same coin are incompatible, leading to internal conflicts. There is a discrepancy between what participants want and what they do . As a result of these factors, the majority feels dependent on others and have thereby become reactive. Most participants are not inclined to take responsibility themselves but await action and initiatives from others. This may explain why NHST is still the standard and used by almost everyone involved.

The current study is closely related to the longstanding debate regarding NHST which recently increased to a level not seen before. In 2015, the editors of the journal ‘Basic and Applied Social Psychology’ (BASP) prohibited the use of NHST (and p-values and confidence intervals) [ 30 ]. Subsequently, in 2016, the American Statistical Association published the so-called ‘Statement on p-values’ in the American Statistician. This statement consists of critical standpoints regarding the use of NHST and p-values and warns against the abuse of the procedure. In 2019, the American Statistician devoted an entire edition to the implementation of reforms regarding the use of NHST; in more than forty articles, scientists debated statistical significance, advocated to embrace uncertainty, and suggested alternatives such as the use of s-values, False Positive Risks, reporting results as effect sizes and confidence intervals and more holistic approaches to p-values and outcome measures [ 31 ]. In addition, in the same year, several articles appeared in which an appeal was made to stop using statistical significance testing [ 32 , 33 ]. A number of counter-reactions were published [ 34 – 36 ], stating (i.e.) that banning statistical significance and, with that, abandoning clear rules for statistical analyses may create new problems with regard to statistical interpretation, study interpretations and objectivity. Also, some methodologists expressed the view that under certain circumstances the use of NHST and p-values is not problematic and can in fact provide useful answers [ 37 ]. Until recently, the NHST-debate was limited to mainly methodologists and statisticians. However, a growing number of scientists are getting involved in this lively debate and believe that a paradigm shift is desirable or even necessary.

The aforementioned publications have constructively contributed to this debate. In fact, since the publication of the special edition of the American Statistician, numerous scientific journals published editorials or revised, to a greater or lesser extent, their author guidelines [ 38 – 45 ]. Furthermore, following the American Statistical Association (ASA), the National Institute of Statistical Sciences (NISS) in the United States has also taken up the reform issue. However, real changes are still barely visible. It takes a long time before these kinds of initiatives translate into behavioral changes, and the widespread adoption by most of the scientific community is still far from accomplished. Debate alone will not lead to real changes, and therefore, our efforts to elucidate behavioral barriers and facilitators could provide a framework for potential effective initiatives that could be taken to reduce the default use of NHST. In fact, the debate could counteract behavioral change. If there is no consensus among statisticians and methodologists (the innovators), changing behavior cannot be expected from stakeholders with less statistical and methodological expertise. In other words, without agreement among innovators, early adopters might be reluctant to adopt the innovation.

Research has recently been conducted to explore the potential of behavioral change to improve Open Science behaviors. The adoption of open science behavior has increased in the last years, but uptake has been slow, due to firm barriers such as a lack of awareness about the subject, concerns about constrainment of the creative process, worries about being “scooped” and holding on to existing working practices [ 46 ]. The development regarding open science practices and the parallels these lines of research shows with the current study, might be of benefit to subserve behavioral change regarding the use of statistical methods.

The described obstacles to change behavior are related to features of both the ‘innovative idea’ and the potential adopters of the idea. First, there are characteristics of ‘the innovation’ that form barriers. The first barrier is the complexity of the innovation: most participants perceive alternative methods as difficult to understand and to use. A second barrier concerns the feasibility of trying the innovation; most people do not feel flexible about trying out or experimenting with the new idea. There is a lack of time and monetary resources to get acquainted with alternative methods (for example, by following a course). Also, the possible negative consequences of the use of alternatives (lower publications chances, the chance that the statistical method and message is too complicated for one’s readership) is holding people back from experimenting with these alternatives. And lastly, it is unclear for most participants what the visibility of the results of the new idea are. Up until now, the debate has mainly taken place among a small group of statisticians and methodologists. Many researchers are still not aware of the NHST debate and the idea to shift away from NHST and use alternative methods instead. Therefore, the question is how easily the benefits of the innovation can be made visible for a larger part of the scientific community. Thus, our study shows that, although the compatibility of the innovation is largely consistent with existing values (participants are critical about (the use of) NHST and the p-value and believe that there are better alternatives to NHST), important attributes of the innovative idea negatively affect the rate of adoption and consequently the diffusion of the innovation.

Due to the barriers mentioned above, most stakeholders do not have the intention to change their behavior and adopt the innovative idea. From the theory of planned behavior [ 21 ], it is known that behavioral intentions directly relate to performances of behaviors. The strength of the intention is shaped by attitudes, subjective norms, and perceived power. If people evaluate the suggested behavior as positive (attitude), and if they think others want them to perform the behavior (subjective norm), this leads to a stronger intention to perform that behavior. When an individual also perceives they have enough control over the behavior, they are likely to perform it. Although most participants have a positive attitude towards the behavior, or the innovative idea at stake, many participants think that others in their working environment believe that they should not perform the behavior—i.e., they do not approve of the use of alternative methods (social normative pressure). This is expressed, for example, in lower publication chances, negative judgements by supervisors or failing the requirements that are imposed by funding agencies. Thus, the perception about a particular behavior—the use of alternative methods—is negatively influenced by the (perceived) judgment of others. Moreover, we found that many participants have a low self-efficacy, meaning that there is a perceived lack of behavioral control, i.e., their perceived ability to engage in the behavior at issue is low. Also, participants feel a lack of authority (in the sense of knowledge and skills, but also power) to initiate behavioral change. The existing subjective norms and perceived behavioral control, and the negative attitudes towards performing the behavior, lead to a lower behavioral intention, and, ultimately, a lower chance of the performance of the actual behavior.

Several participants mentioned there is a need for people of stature (belonging to the group of early adopters) to take the lead and break down perceived barriers. Early adopters serve as role models and have opinion leadership, and form the next group (after the innovators, in this case statisticians and methodologists) to adopt an innovative idea [ 20 ] ( Fig 2 ). If early adopters would stand up, conveying a positive attitude towards the innovation, breaking down the described perceived barriers and facilitating the use of alternatives (for example by adjusting policy, guidelines and educational programs and making available financial resources for further training), this could positively affect the perceived social norms and self-efficacy of the early and late majority and ultimately laggards, which could ultimately lead to behavioral change among all stakeholders within the scientific community.

A strength of our study is that it is the first empirical study on views on the use of NHST, its alternatives and reasons for the prevailing use of NHST. Another strength is the method of coding which corresponds to the thematic approach from Braun & Clarke [ 47 ], which allows the researcher to move beyond just categorizing and coding the data, but also analyze how the codes are related to each other [ 47 ]. It provides a rich description of what is studied, linked to theory, but also generating new hypotheses. Moreover, two independent researchers coded all transcripts, which adds to the credibility of the study. All findings and the coding scheme were discussed by the two researchers, until consensus was reached. Also, interview results were further explored, enriched and validated by means of (mixed) focus groups. Important themes that emanated from the interviews, such as interdependency, perceptions on the scientific duty, perceived disadvantages of alternatives or the consequences of the current scientific climate, served as starting points and main subjects of the focus groups. This set-up provided more data, and more insight about the data and validation of the data. Lastly, the use of a theoretical framework [ 20 , 21 ] to develop the topic list, guide the interviews and focus groups, and guide their analysis is a strength as it provides structure to the analysis and substantiation of the results.

A limitation of this study is its sampling method. By using the network of members of the project group, and the fact that a relatively high proportion of those invited to participate refused because they thought they knew too little about the subject to be able to contribute, our sample was biased towards participants that are (somewhat) aware of the NHST debate. Our sample may also consist of people that are relatively critical towards the use of NHST, compared to the total population of researchers. It was not easy to include participants who were indifferent about or who were pro-NHST, as those were presumably less willing to make time and participate in this study. Even in our sample we found that the majority of our participants solely used NHST and perceived it as difficult if not impossible to change their behavior. These perceptions are thus probably even stronger in the target population. Another limitation, that is inherent to qualitative research, is the risk of interviewer bias. Respondents are unable, unwilling, or afraid to answer questions in good conscience, and instead provide socially desirable answers. In the context of our research, people are aware that, especially as a scientist, it does not look good to be conservative, complacent, or ignorant, or not to be open to innovation and new ideas. Therefore, some participants might have given a too favorable view of themselves. The interviewer bias can also take the other direction when values and expectations of the interviewer consciously or unconsciously influence the answers of the respondents. Although we have tried to be as neutral and objective as possible in asking questions and interpreting answers, we cannot rule out the chance that our views and opinions on the use of NHST have at times steered the respondents somewhat, potentially leading to the foregoing desirable answers.

Generalizability is a topic that is often debated in qualitative research methodology. Many researchers do not consider generalizability the purpose of qualitative research, but rather finding in-depth insights and explanations. However, this is an unjustified simplification, as generalizing of findings from qualitative research is possible. Three types of generalization in qualitative research are described: representational generalization (whether what is found in a sample can be generalized to the parent population of the sample), inferential generalization (whether findings from the study can be generalized to other settings), and theoretical generalization (where one draws theoretical statements from the findings of the study for more general application) [ 48 ]. The extent to which our results are generalizable is uncertain, as we used a theoretical sampling method, and our study was conducted exclusively in the Netherlands. We expect that the generic themes (reactivity, the scientific duty and the scientific climate) are applicable to academia in many countries across the world (inferential generalization). However, some elements, such as the Dutch educational system, will differ to a more or lesser extent from other countries (and thus can only be representationally generalized). In the Netherlands there is, for example, only one educational route after secondary school that has an academic orientation (scientific education, equivalent to the US university level education). This route consists of a bachelor’s program (typically 3 years), and a master’s program (typically 1, 2 or 3 years). Not every study program contains (compulsory) statistical courses, and statistical courses differ in depth and difficulty levels depending on the study program. Thus, not all the results will hold for other parts of the world, and further investigation is required.

Our findings demonstrate how perceived barriers to shift away from NHST set a high threshold for behavioral change and create a circle of interdependency. Behavioral change is a complex process. As ‘the stronger the intention to engage in a behavior, the more likely should be its performance’[ 21 ], further research on this subject should focus on how to influence the intention of behavior; i.e. which perceived barriers for the use of alternatives are most promising to break down in order to increase the intention for behavioral change. The present study shows that negative normative beliefs and a lack of perceived behavioral control regarding the innovation among individuals in the scientific system is a substantial problem. When social norms change in favor of the innovation, and control over the behavior increases, then the behavioral intention becomes a sufficient predictor of behavior [ 49 ]. An important follow-up question will therefore be: how can people be enthused and empowered, to ultimately take up the use of alternative methods instead of NHST? Answering this question can, in the long run, lead to the diffusion of the innovation through the scientific system as a whole.

NHST has been the leading paradigm for many decades and is deeply rooted in our science system, despite longstanding criticism. The aim of this study was to gain insight as to why we continue to use NHST. Our findings have demonstrated how perceived barriers to make a shift away from NHST set a high threshold for actual behavioral change and create a circle of interdependency between stakeholders in the scientific system. Consequently, people find themselves in a state of reactivity, which limits behavioral change with respect to the use of NHST. The next step would be to get more insight into ways to effectively remove barriers and thereby increase the intention to take a step back from NHST. A paradigm shift within a couple of years is not realistic. However, we believe that by taking small steps, one at a time, it is possible to decrease the scientific community’s strong dependence on NHST and p-values.

Supporting information

S1 appendix, acknowledgments.

The authors are grateful to Anja de Kruif for her contribution to the design of the study and for moderating one of the focus groups.

Funding Statement

This research was funded by the NWO (Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Dutch Organization for Scientific Research) ( https://www.nwo.nl/ ) The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Data Availability

  • Open access
  • Published: 29 May 2024

Knowledge, attitudes, and practices of primary healthcare practitioners regarding pharmacist clinics: a cross-sectional study in Shanghai

  • Xinyue Zhang 1   na1 ,
  • Zhijia Tang 1   na1 ,
  • Yanxia Zhang 1   na1 ,
  • Wai Kei Tong 1 ,
  • Qian Xia 1 ,
  • Bing Han 1 &
  • Nan Guo 1  

BMC Health Services Research volume  24 , Article number:  677 ( 2024 ) Cite this article

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Pharmacist clinics offer professional pharmaceutical services that can improve public health outcomes. However, primary healthcare staff in China face various barriers and challenges in implementing such clinics. To identify existing problems and provide recommendations for the implementation of pharmacist clinics, this study aims to assess the knowledge, attitudes, and practices of pharmacist clinics among primary healthcare providers.

A cross-sectional survey based on the Knowledge-Attitude-Practice (KAP) model, was conducted in community health centers (CHCs) and private hospitals in Shanghai, China in May, 2023. Descriptive analytics and the Pareto principle were used to multiple-answer questions. Chi-square test, Fisher’s exact test, and binary logistic regression models were employed to identify factors associated with the knowledge, attitudes, and practices of pharmacist clinics.

A total of 223 primary practitioners participated in the survey. Our study revealed that most of them had limited knowledge (60.1%, n  = 134) but a positive attitude (82.9%, n  = 185) towards pharmacist clinics, with only 17.0% ( n  = 38) having implemented them. The primary goal of pharmacist clinics was to provide comprehensive medication guidance (31.5%, n  = 200), with medication education (26.3%, n  = 202) being the primary service, and special populations (24.5%, n  = 153) identified as key recipients. Logistic regression analysis revealed that education, age, occupation, position, work seniority, and institution significantly influenced their perceptions. Practitioners with bachelor’s degrees, for instance, were more likely than those with less education to recognize the importance of pharmacist clinics in medication guidance (aOR: 7.130, 95%CI: 1.809–28.099, p -value = 0.005) and prescription reviews (aOR: 4.675, 95% CI: 1.548–14.112, p -value = 0.006). Additionally, practitioners expressed positive attitudes but low confidence, with only 33.3% ( n  = 74) feeling confident in implementation. The confidence levels of male practitioners surpassed those of female practitioners ( p -value = 0.037), and practitioners from community health centers (CHCs) exhibited higher confidence compared to their counterparts in private hospitals ( p -value = 0.008). Joint physician-pharmacist clinics (36.8%, n  = 82) through collaboration with medical institutions (52.0%, n  = 116) emerged as the favored modality. Daily sessions were preferred (38.5%, n  = 86), and both registration and pharmacy service fees were considered appropriate for payment (42.2%, n  = 94). The primary challenge identified was high outpatient workload (30.9%, n  = 69).

Conclusions

Although primary healthcare practitioners held positive attitudes towards pharmacist clinics, limited knowledge, low confidence, and high workload contributed to the scarcity of their implementation. Practitioners with diverse sociodemographic characteristics, such as education, age, and institution, showed varying perceptions and practices regarding pharmacist clinics.

Peer Review reports

Pharmacist clinics are specialized healthcare facilities that offer professional pharmaceutical services, such as medication therapy management, medication reconciliation, lifestyle counseling, and immunizations, for patients with chronic diseases or managing multiple drugs [ 1 ]. Through the provision of these services, pharmacist clinics aim to improve patient access to healthcare, optimize medication use, and improve overall public health outcomes.

Pharmacist clinics originated in the 1960s in the United States and have spread globally in recent decades [ 2 ], with a growing number of countries adopting this model of care. The World Health Organization (WHO) has recognized the importance of pharmacists in primary healthcare and encouraged the integration of pharmaceutical services into broader healthcare systems [ 3 ]. This integration facilitates the rational use of medication, thereby minimizing adverse drug events and medication errors, ultimately leading to better therapeutic outcomes. Moreover, pharmacist clinics offer medication guidance and education, which adjusts optimal medication dosage [ 4 ], enhances patient adherence [ 1 , 5 ], expands access to health care [ 6 ], and reduces treatment costs [ 7 ]. These clinics effectively bridge the communication gap between physicians and pharmacists [ 8 ], fostering interdisciplinary collaboration and integrated patient care [ 1 , 9 ].

The development of pharmacist clinics in China was initiated in the late 20th century, coinciding with the introduction of healthcare reforms by the Chinese government in the early 2000s. The release of “Opinions on Deepening the Reform of the Medical and Health System” [ 10 ] in 2009 highlighted the importance of pharmacist clinics and the crucial role of pharmacists in improving the quality and accessibility of healthcare services in primary settings. In 2020, the Chinese government released a guidance document titled “Opinions on Strengthening the Pharmaceutical Management of Medical Institutions and Promoting Rational Drug Use,” encouraging provinces to actively establish pharmacist clinics [ 11 ]. However, it wasn’t until 2021 that the General Office of the National Health Commission developed the “Guidelines for Pharmaceutical Outpatient Services in Medical Institutions” to standardize these pharmacist clinics [ 12 ]. Despite the progress made, primary medical staff in both developed and developing countries face various challenges, especially in developing countries [ 13 ], including a shortage of qualified pharmacists [ 14 , 15 ], limited recognition of pharmacists’ roles among healthcare professionals and the public [ 16 , 17 ], and the need for a more standardized approach to pharmaceutical care [ 18 ]. Additionally, these clinics are predominantly located in large general hospitals or specialized medical facilities, limiting their coverage to specific areas, such as antibiotics [ 19 ] and anticoagulants [ 20 ]. In rural areas, there is scarce awareness and discussion regarding the promotion of pharmacist clinics.

To date, most research on pharmacist clinics comes from countries like the United States, the UK, Canada, and Australia, focusing primarily on the outcomes of pharmacist interventions rather than the implementation challenges [ 1 , 4 , 21 , 22 , 23 , 24 ]. In China, only a few studies have assessed the current state of pharmacist clinics. Cai et al. [ 25 ], for instance, conducted a national survey revealing that just 10.03% of hospitals had pharmacist clinics. Wu et al. [ 26 ] investigated the establishment and operational details of pharmacist-managed clinics in Taiwan. However, there is no published research exploring optimal practices for setting up pharmacist clinics in China or identifying the barriers to establishing these clinics in primary healthcare settings. In this study, we aim to assess the awareness and understanding of pharmacist clinics among primary healthcare providers. We conducted a cross-sectional survey based on the Knowledge-Attitude-Practice (KAP) model to identify knowledge gaps and develop interventions to encourage interprofessional collaboration and enhance practice efficiency. The findings may also improve patient outcomes, healthcare delivery by streamlining the implementation process, and utilization of high-quality pharmaceutical services. Our ultimate goal was to overcome barriers to advancing pharmacist clinics within China’s healthcare system and offer insights for policymakers and healthcare authorities to integrate these clinics into primary healthcare settings, not only in China but potentially in other countries as well.

Survey instrument & selection criteria

Our study employed a structural equation model based on the Knowledge, Attitude, and Practice (KAP) theory [ 27 ] and relevant literature [ 28 , 29 , 30 , 31 ] to explore the relationships between various factors. Following the KAP principles, we developed a questionnaire consisting of 21 questions across three domains: (A) knowledge of pharmacist clinics, (B) attitudes towards pharmacist clinics, and (C) practices related to pharmacist clinics. Demographic information such as gender, age, education, occupation, position, seniority, department, and institution was collected through self-reporting.

The inclusion and exclusion criteria for the sampled respondents were as follows. Inclusion criteria: (1) Full-time primary healthcare practitioners attending a continuing education course at Minhang Hospital in Shanghai, China. This included physicians, pharmacists, nurses, and other primary healthcare practitioners. (2) Willingness to participate in the study and provide informed consent. Exclusion criteria: (1) Part-time employees or interns. (2) Non-medical staff. (3) Individuals who declined to sign the informed consent form.

Study population and data source

This study used data from a cross-sectional survey conducted in May, 2023, involving primary healthcare practitioners from 10 community health centers (CHCs) and 38 private hospitals in Shanghai, China. After excluding participants from secondary or tertiary hospitals ( n  = 9), nursing homes ( n  = 6), and other facilities such as welfare homes and school clinics ( n  = 9), a total of 223 eligible subjects were included.

Data collection

The sample size was optimized to range between 105 and 210, based on the recommended ratio of 5 to 10 respondents per item [ 32 , 33 ]. We also performed a pilot study in April, 2023 to ensure linguistic clarity and readability of the questionnaire. Twenty-six student volunteers from the School of Pharmacy at Fudan University were recruited to refine the questionnaire. Additionally, face-to-face interviews were conducted to further assess their understanding of the content. The final version was electronically distributed to participants during a continuing education course using a voluntary sampling approach. The full questionnaire is available in Supplementary Table 1 , and all data were anonymized.

Statistical analysis

Categorical variables were summarized using frequency counts (weighted percentage, %). The Chi-square test and Fisher’s exact test were used to assess differences in knowledge, attitude, and practice regarding pharmacist clinics across various sociodemographic characteristics. Descriptive analytics and the Pareto principle were applied to multiple-answer questions. In case of rejection of the null hypothesis, multiple pairwise comparisons would be conducted as confirmatory post hoc analysis using Bonferroni correction. Based on the univariate analysis results, we constructed binary logistic regression models to calculate adjusted odds ratios (aOR) and 95% confidence intervals (CI) to reveal factors associated with perceived goals, service scope, and target recipients of pharmacist clinics.

All statistical analyses were performed using IBM SPSS Statistics for Windows, Version 20.0 (IBM Corp., Armonk, NY, USA). A two-sided p -value < 0.05 was considered statistically significant.

Demographics

As presented in Table  1 , a total of 223 primary healthcare practitioners participated in the survey, with 41.3% ( n  = 92) being male and 76.2% ( n  = 170) under 45 years old. The majority (84.3%, n  = 188) were physicians, while the remaining were pharmacists. Regarding educational qualifications, 82.5% ( n  = 184) of respondents held a bachelor’s degree or below. Furthermore, 91.9% ( n  = 205) held mid-level or lower positions, and 56.1% ( n  = 125) reported professional tenures of less than 10 years. Of these 223 practitioners, 36.8% ( n  = 82) were from public institutions (community health centers), and 63.2% ( n  = 141) were from private hospitals.

Knowledge of pharmacist clinics

Of primary care practitioners, 84.8% ( n  = 189) recognized pharmacist clinics, with 24.7% ( n  = 55) having strong familiarity. Figure  1 a-c showed practitioners’ views on the goals, services, and target recipients of these clinics. The primary goal was to provide comprehensive medication guidance (31.5%, n  = 200), with medication education (26.3%, n  = 202) being the primary service, and special populations (24.5%, n  = 153) identified as key recipients. Logistic regression results revealed several significant influential factors (Table  2 ).

figure 1

Pareto chart demonstrating respondents’ knowledge of pharmacist clinics

( a ) Perceived goals: A prescription reviews, B medication guidance, C time-saving, D conflict alleviation, E patient empowerment, F cost reduction, G role enhancement, H research, I training, and J no perceived value

( b ) Perceived service scope: A drug regimen adjustments, B medication reconciliation, C medication education on dosage, side effects, and interactions, D adherence interventions, E health promotion, F patient follow-ups

( c ) Perceived target recipients: A isolated/empty-nest patients, B special populations (e.g. elderly, children, pregnant, and liver/kidney-impaired), C economically disadvantaged patients, D patients suffering from adverse reactions, E patients needing test report interpretations, F frequent drug collectors (> 20 times/year), G patients with ≥ 2 chronic diseases, H patients with any chronic diseases, I patients on ≥ 5 medications, J high-risk drug users (e.g. psychotropic drugs, hormones, injections, and inhalants), K patients under contract with family physicians, and L all patients

Compared to those with less education, practitioners with bachelor’s degrees were more likely to see the role of pharmacist clinics in medication guidance (aOR: 7.130, 95%CI: 1.809–28.099, p -value = 0.005), prescription reviews (aOR: 4.675, 95% CI: 1.548–14.112, p -value = 0.006), and serving patients on high-risk drugs (aOR: 2.824, 95% CI: 1.090–7.316, p -value = 0.033).

Besides medication guidance (aOR: 7.303, 95%CI: 1.343–39.720, p -value = 0.021), practitioners with master’s or higher degrees preferred adherence interventions (aOR: 4.221, 95%CI: 1.339–13.300, p -value = 0.014), follow-up services (aOR: 3.125, 95%CI: 1.095–8.915, p -value = 0.033), and catering to patients with ≥ 2 chronic diseases (aOR: 6.401, 95%CI: 1.233–33.223, p -value = 0.027) or ≥ 5 medications (aOR: 3.987, 95%CI: 1.250-12.717, p -value = 0.019). Higher education was also inversely associated with emphasizing patients needing test report interpretations (aOR < 1, p -value < 0.05).

Younger practitioners, aged 18 to 30, considered pharmacist clinics as tools to mitigate physician-patient conflicts through improved communication compared to those aged ≥ 46 (aOR: 0.165, 95%CI: 0.028–0.988, p -value = 0.048).

Compared to physicians, pharmacists typically addressed all patients as recipients (aOR: 3.322, 95%CI: 1.031–10.703, p -value = 0.044), but were less likely to offer drug regimen adjustments (aOR: 0.210, 95%CI: 0.088-0.500, p -value < 0.001).

Junior and intermediate-level practitioners demonstrated a greater likelihood for follow-up services (aOR 1 : 5.832, 95%CI: 1.308–25.998, p -value = 0.021; aOR 2 : 3.99, 95%CI: 1.087–14.646, p -value = 0.037), and were less likely to target patients in need of test report interpretations (aOR 1 : 0.172, 95%CI: 0.038–0.781, p -value = 0.023; aOR 2 : 0.287, 95%CI: 0.082–0.997, p -value = 0.049) than their senior counterparts.

Work seniority

Practitioners with 10–19 years of work experience were significantly more likely to consider isolated/empty-nest patients as suitable recipients compared to those with < 5 years of experience (aOR: 3.328, 95%CI: 1.021–10.849, p -value = 0.046).

Institution

Practitioners from CHCs were more likely to view frequent drug collectors as suitable recipients compared to those from private hospitals (aOR: 0.359, 95%CI: 0.134–0.966, p -value = 0.043).

Attitude of pharmacist clinics

Necessity and confidence in implementing pharmacist clinics.

Table  3 showed that 82.9% ( n  = 185) of practitioners recognized the necessity of pharmacist clinics, but only 33.3% ( n  = 75) felt confident in their implementation. Male practitioners exhibited significantly higher confidence levels compared to female practitioners ( p  = 0.037), and practitioners from community health centers (CHCs) showed greater confidence relative to those practicing in private hospitals ( p  = 0.008).

Preferred mode of pharmacist clinics

As shown in Table  4 , the favored modality was found to be joint physician-pharmacist clinics (36.8%, n  = 82), through collaboration with medical institutions (52.0%, n  = 116). Daily sessions emerged as the preferred frequency ( n  = 86, 38.5%), with both registration and pharmacy service fees considered appropriate for payment (42.2%, n  = 94).

Furthermore, we explored the influence of different sociodemographic variables. Practitioners holding a master’s degree or higher demonstrated a preference for a clinic frequency of 2–4 times per week ( p -value = 0.015), along with acceptance of both registration and pharmacy service fees ( p -value < 0.001), compared to those with lower levels of education. Conversely, those with a junior college education or below were more willing to seek free services. Practitioners from CHCs exhibited a preference for weekly or 2–4 times per week clinics, whereas those from private hospitals favored daily or monthly sessions ( p -value < 0.001).

Practice of pharmacist clinics

As shown in Table  5 , there was a limited prevalence of pharmacist clinics within primary care institutions. Only 17.0% ( n  = 38) of practitioners reported the implementation of pharmacy clinics, mostly scheduled once a week (47.4%, n  = 18), with the primary challenge being a high outpatient workload (30.9%, n  = 69). Practitioners from CHCs demonstrated a significantly higher implementation frequency compared to those from private hospitals ( p -value < 0.001).

We further explored sociodemographic factors associated with challenges. Practitioners aged over 45 years ( P  = 0.020) and occupying senior/deputy senior positions ( p -value = 0.018) were more likely to consider the absence of fee collection mechanisms as the principal difficulty, as opposed to their younger counterparts and those in lower positions.

Our study aims to evaluate the perceptions, attitudes, and practices of primary healthcare practitioners regarding pharmacist clinics and to identify necessary changes. The findings unveiled a lack of knowledge and confidence among primary care providers, who are faced with barriers including high outpatient workloads and concerns related to professionalism. Collaborative models are preferred as they align with the current emphasis on multidisciplinary approaches in modern healthcare, which aim to achieve optimal population health [ 34 ]. Additionally, our findings highlight the impact of institution and gender on the perceptions of primary care providers.

In this study, more practitioners preferred joint physician-pharmacist clinics over traditional physician-led clinics (36.8%, n  = 82 vs. 24.2%, n  = 54), which is in line with a global focus on integrating pharmacists into the provision of patient-centered, coordinated, and comprehensive care [ 1 , 35 , 36 ]. Primary care physicians are in short supply, and studies unveiled that the shortage of primary care physicians has led to increased workloads and a greater demand for medication guidance services, especially among vulnerable patients aged 65 and above [ 37 , 38 , 39 , 40 ]. Our study showed the primary goals of pharmacist clinics were found to be prescription reviews (28.9%, n  = 183) and medication guidance (31.5%, n  = 200), which are critical in addressing concerns regarding poorly managed or duplicate prescriptions [ 41 , 42 ]. Integrating pharmaceutical services into primary care offers expedited access and convenience for patients, thereby releasing physicians to focus on more complex cases and reducing their workload [ 43 , 44 ]. These services also contribute to overall savings in healthcare and medication costs, as well as reduced general physician appointments, emergency department visits, and inappropriate drug use [ 45 , 46 ]. Our findings support the potential of pharmacist-led prescription reviews in reducing duplicate prescriptions [ 47 ], drug-related problems [ 48 ], and medication costs, without increasing physicians’ workload [ 49 ]. Moreover, pharmacist-led medication guidance provided to other professionals has been shown to reduce medication errors and inappropriate prescriptions compared to standard care [ 50 , 51 ]. The development of joint physician-pharmacist clinics may be an advantageous choice for the development of pharmacist clinics in the future.

Current evidence highlights the suboptimal quality of primary care in China [ 52 ], with previous research suggesting that inadequate education and training pose significant challenges in enhancing care quality [ 53 ]. Primary healthcare providers in China have reported being too busy for continued education, dissatisfaction with course content, and having unqualified supervisors [ 54 ]. This issue seems to be consistent in the United States [ 55 ], Canada [ 56 ], and Belgium [ 57 ]. Moreover, our study has identified high workload (30.9%, n  = 69) and insufficient professionalism (25.1%, n  = 56) as the top two challenges faced by pharmacist clinics. On the other hand, insufficient knowledge may contribute to negative attitudes [ 39 ].

In this study, a minority of practitioners (24.7%, n  = 55) demonstrated strong familiarity, and only 33.3% ( n  = 75) felt confident. While some global studies did not find a significant difference in clinical competence confidence between public and private practitioners [ 58 , 59 ], our study revealed that pharmacists from CHCs exhibited greater confidence in conducting pharmacist clinics compared to those from private hospitals, partially due to their greater exposure to training. Studies have also shown that community pharmacists, through enhanced training, can acquire expanded expertise and knowledge [ 60 , 61 ], leading to improved service quality in primary care [ 62 , 63 ]. Future efforts should focus on establishing a more efficient learning and continued education system for community practitioners in China [ 52 ].

Several impediments were identified by respondents, including limited patient volume (22.0%, n  = 49) and low staff motivation (6.3%, n  = 14). Despite the positive impact of pharmacists in outpatient settings on patient outcomes, the adoption of these services remains low [ 1 ]. Recent literature has highlighted public uncertainty about primary care specialties and skepticism regarding their capacity to deliver comprehensive care [ 64 ]. Evidence suggests a lack of awareness, demand, and utilization of community pharmacy services among patients [ 65 , 66 ]. Another barrier is the prevailing focus on quantity rather than quality of care, with job content and bonuses linked more to quantity than the quality of care delivered [ 52 , 67 ]. Financial conflicts over funding and the absence of fee collection may also hinder collaboration between pharmacists and other healthcare providers [ 43 , 68 ]. Additionally, the implementation of the zero-mark-up drug policy in China in 2011 caused a substantial decrease of about 40% in drug-related incomes [ 69 ]. Institutions responded by scaling back clinical care services to offset this profit loss [ 70 ], leading to an uptick in hospital visits for minor ailments and further burdening the healthcare system [ 53 ]. It is important to expand community pharmacy services by establishing reimbursement mechanisms to relieve the burden on general practice [ 71 ]. Countries like Australia, the UK, New Zealand, and Canada have established systems for pharmacist remuneration [ 72 ]. Payment models for pharmaceutical services typically include fee-for-service, where providers are compensated based on the services delivered (as seen in Australia, Canada, Belgium, and Japan), capitation, where providers receive a fixed amount per patient (as in the US, Thailand, and Denmark), and blended funding, which combines government and private payments (as in China, Australia, New Zealand, and Canada) [ 73 ]. Despite the existence of various payment models for pharmaceutical services, there is no standardized pricing for pharmacist clinics. Among 465 hospitals with pharmacist clinics, only 98 (21.08%) owned charging mechanisms [ 25 ]. Various studies have explored the willingness to pay (WTP) for pharmaceutical services in different countries. For instance, Porteous et al. [ 74 ] found a WTP of $69.19 for community practices in the UK. Tsao et al. [ 75 ] reported a WTP of $21.26 for medication therapy management in Canada, and in Brazil, the estimated WTP for comprehensive medication management was $17.75 [ 76 ].

Our findings also revealed gender-based disparities in the perceptions and implementation of pharmacist clinics. Female practitioners exhibited lower levels of confidence in conducting the clinics compared to males, consistent with previous research indicating that women in healthcare often perceive deficiencies in their abilities despite no differences in clinical performance between genders [ 77 ]. Additionally, female medical students reported higher levels of anxiety, stress, and self-doubt about their knowledge and performance [ 78 ]. However, in Australia and Ireland, females rated themselves higher than males in self-assessment tests [ 79 , 80 ]. Further investigations to explore potential confounding factors, such as cultural influences, may contribute to understanding these variations and better address the need to tailor pharmacist-managed clinic services based on institutional needs [ 81 ].

This research is geographically confined to Shanghai and solely captures the perspectives of practitioners, potentially limiting generalizability. Future studies should broaden their scope to encompass diverse practices and include patients’ perceptions. The cross-sectional design used in this study restricts the evaluation of cause-effect relationships, emphasizing the need for longitudinal investigations. Despite these limitations, to the best of the authors’ knowledge, this is the first quantitative study that has examined the knowledge, attitudes, and practice of practitioners regarding pharmacist clinics in primary settings based on real-world data in China. The identified challenges in conducting these clinics provide valuable insights for policymakers, researchers, and institutions in this field.

Although primary healthcare practitioners generally hold positive attitudes towards pharmacist clinics, limited knowledge and confidence, high workload, and other factors lead to the scarcity of such clinics. Practitioners with diverse sociodemographic backgrounds, especially those from different institutions and genders, exhibit varying perceptions of the forms of pharmacist clinics. Further exploration with lager samples from different regions and service recipients is necessary.

Data availability

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

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We thank all the participants in this research.

This study received funding from the Shanghai Committee of Science and Technology (Grant No. 22YF1439800) and the Shanghai Municipal Health Commission (Grant No. 20194Y0234).

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Xinyue Zhang, Zhijia Tang, Yanxia Zhang, Wai Kei Tong, Qian Xia, Bing Han & Nan Guo

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ZT and YZ designed the research, developed the questionnaire; WT and QX collected the data; XZ and ZT performed the statistical analysis and wrote the manuscript; BH and NG critically reviewed the statistical analysis, work, and this report. All authors read and approved the final manuscript.

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Zhang, X., Tang, Z., Zhang, Y. et al. Knowledge, attitudes, and practices of primary healthcare practitioners regarding pharmacist clinics: a cross-sectional study in Shanghai. BMC Health Serv Res 24 , 677 (2024). https://doi.org/10.1186/s12913-024-11136-3

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Current status of community resources and priorities for weed genomics research

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Weeds are attractive models for basic and applied research due to their impacts on agricultural systems and capacity to swiftly adapt in response to anthropogenic selection pressures. Currently, a lack of genomic information precludes research to elucidate the genetic basis of rapid adaptation for important traits like herbicide resistance and stress tolerance and the effect of evolutionary mechanisms on wild populations. The International Weed Genomics Consortium is a collaborative group of scientists focused on developing genomic resources to impact research into sustainable, effective weed control methods and to provide insights about stress tolerance and adaptation to assist crop breeding.

Each year globally, agricultural producers and landscape managers spend billions of US dollars [ 1 , 2 ] and countless hours attempting to control weedy plants and reduce their adverse effects. These management methods range from low-tech (e.g., pulling plants from the soil by hand) to extremely high-tech (e.g., computer vision-controlled spraying of herbicides). Regardless of technology level, effective control methods serve as strong selection pressures on weedy plants and often result in rapid evolution of weed populations resistant to such methods [ 3 , 4 , 5 , 6 , 7 ]. Thus, humans and weeds have been locked in an arms race, where humans develop new or improved control methods and weeds adapt and evolve to circumvent such methods.

Applying genomics to weed science offers a unique opportunity to study rapid adaptation, epigenetic responses, and examples of evolutionary rescue of diverse weedy species in the face of widespread and powerful selective pressures. Furthermore, lessons learned from these studies may also help to develop more sustainable control methods and to improve crop breeding efforts in the face of our ever-changing climate. While other research fields have used genetics and genomics to uncover the basis of many biological traits [ 8 , 9 , 10 , 11 ] and to understand how ecological factors affect evolution [ 12 , 13 ], the field of weed science has lagged behind in the development of genomic tools essential for such studies [ 14 ]. As research in human and crop genetics pushes into the era of pangenomics (i.e., multiple chromosome scale genome assemblies for a single species [ 15 , 16 ]), publicly available genomic information is still lacking or severely limited for the majority of weed species. Recent reviews of current weed genomes identified 26 [ 17 ] and 32 weed species with sequenced genomes [ 18 ]—many assembled to a sub-chromosome level.

Here, we summarize the current state of weed genomics, highlighting cases where genomics approaches have successfully provided insights on topics such as population genetic dynamics, genome evolution, and the genetic basis of herbicide resistance, rapid adaptation, and crop dedomestication. These highlighted investigations all relied upon genomic resources that are relatively rare for weedy species. Throughout, we identify additional resources that would advance the field of weed science and enable further progress in weed genomics. We then introduce the International Weed Genomics Consortium (IWGC), an open collaboration among researchers, and describe current efforts to generate these additional resources.

Evolution of weediness: potential research utilizing weed genomics tools

Weeds can evolve from non-weed progenitors through wild colonization, crop de-domestication, or crop-wild hybridization [ 19 ]. Because the time span in which weeds have evolved is necessarily limited by the origins of agriculture, these non-weed relatives often still exist and can be leveraged through population genomic and comparative genomic approaches to identify the adaptive changes that have driven the evolution of weediness. The ability to rapidly adapt, persist, and spread in agroecosystems are defining features of weedy plants, leading many to advocate agricultural weeds as ideal candidates for studying rapid plant adaptation [ 20 , 21 , 22 , 23 ]. The insights gained from applying plant ecological approaches to the study of rapid weed adaptation will move us towards the ultimate goals of mitigating such adaptation and increasing the efficacy of crop breeding and biotechnology [ 14 ].

Biology and ecological genomics of weeds

The impressive community effort to create and maintain resources for Arabidopsis thaliana ecological genomics provides a motivating example for the emerging study of weed genomics [ 24 , 25 , 26 , 27 ]. Arabidopsis thaliana was the first flowering plant species to have its genome fully sequenced [ 28 ] and rapidly became a model organism for plant molecular biology. As weedy genomes become available, collection, maintenance, and resequencing of globally distributed accessions of these species will help to replicate the success found in ecological studies of A. thaliana [ 29 , 30 , 31 , 32 , 33 , 34 , 35 ]. Evaluation of these accessions for traits of interest to produce large phenomics data sets (as in [ 36 , 37 , 38 , 39 , 40 ]) enables genome-wide association studies and population genomics analyses aimed at dissecting the genetic basis of variation in such traits [ 41 ]. Increasingly, these resources (e.g. the 1001 genomes project [ 29 ]) have enabled A. thaliana to be utilized as a model species to explore the eco-evolutionary basis of plant adaptation in a more realistic ecological context. Weedy species should supplement lessons in eco-evolutionary genomics learned from these experiments in A. thaliana .

Untargeted genomic approaches for understanding the evolutionary trajectories of populations and the genetic basis of traits as described above rely on the collection of genotypic information from across the genome of many individuals. While whole-genome resequencing accomplishes this requirement and requires no custom methodology, this approach provides more information than is necessary and is prohibitively expensive in species with large genomes. Development and optimization of genotype-by-sequencing methods for capturing reduced representations of newly sequence genomes like those described by [ 42 , 43 , 44 ] will reduce the cost and computational requirements of genetic mapping and population genetic experiments. Most major weed species do not currently have protocols for stable transformation, a key development in the popularity of A. thaliana as a model organism and a requirement for many functional genomic approaches. Functional validation of genes/variants believed to be responsible for traits of interest in weeds has thus far relied on transiently manipulating endogenous gene expression [ 45 , 46 ] or ectopic expression of a transgene in a model system [ 47 , 48 , 49 ]. While these methods have been successful, few weed species have well-studied viral vectors to adapt for use in virus induced gene silencing. Spray induced gene silencing is another potential option for functional investigation of candidate genes in weeds, but more research is needed to establish reliable delivery and gene knockdown [ 50 ]. Furthermore, traits with complex genetic architecture divergent between the researched and model species may not be amenable to functional genomic approaches using transgenesis techniques in model systems. Developing protocols for reduced representation sequencing, stable transformation, and gene editing/silencing in weeds will allow for more thorough characterization of candidate genetic variants underlying traits of interest.

Beyond rapid adaptation, some weedy species offer an opportunity to better understand co-evolution, like that between plants and pollinators and how their interaction leads to the spread of weedy alleles (Additional File 1 : Table S1). A suite of plant–insect traits has co-evolved to maximize the attraction of the insect pollinator community and the efficiency of pollen deposition between flowers ensuring fruit and seed production in many weeds [ 51 , 52 ]. Genetic mapping experiments have identified genes and genetic variants responsible for many floral traits affecting pollinator interaction including petal color [ 53 , 54 , 55 , 56 ], flower symmetry and size [ 57 , 58 , 59 ], and production of volatile organic compounds [ 60 , 61 , 62 ] and nectar [ 63 , 64 , 65 ]. While these studies reveal candidate genes for selection under co-evolution, herbicide resistance alleles may also have pleiotropic effects on the ecology of weeds [ 66 ], altering plant-pollinator interactions [ 67 ]. Discovery of genes and genetic variants involved in weed-pollinator interaction and their molecular and environmental control may create opportunities for better management of weeds with insect-mediated pollination. For example, if management can disrupt pollinator attraction/interaction with these weeds, the efficiency of reproduction may be reduced.

A more complete understanding of weed ecological genomics will undoubtedly elucidate many unresolved questions regarding the genetic basis of various aspects of weediness. For instance, when comparing populations of a species from agricultural and non-agricultural environments, is there evidence for contemporary evolution of weedy traits selected by agricultural management or were “natural” populations pre-adapted to agroecosystems? Where there is differentiation between weedy and natural populations, which traits are under selection and what is the genetic basis of variation in those traits? When comparing between weedy populations, is there evidence for parallel versus non-parallel evolution of weediness at the phenotypic and genotypic levels? Such studies may uncover fundamental truths about weediness. For example, is there a common phenotypic and/or genotypic basis for aspects of weediness among diverse weed species? The availability of characterized accessions and reference genomes for species of interest are required for such studies but only a few weedy species have these resources developed.

Population genomics

Weed species are certainly fierce competitors, able to outcompete crops and endemic species in their native environment, but they are also remarkable colonizers of perturbed habitats. Weeds achieve this through high fecundity, often producing tens of thousands of seeds per individual plant [ 68 , 69 , 70 ]. These large numbers in terms of demographic population size often combine with outcrossing reproduction to generate high levels of diversity with local effective population sizes in the hundreds of thousands [ 71 , 72 ]. This has two important consequences: weed populations retain standing genetic variation and generate many new mutations, supporting weed success in the face of harsh control. The generation of genomic tools to monitor weed populations at the molecular level is a game-changer to understanding weed dynamics and precisely testing the effect of artificial selection (i.e., management) and other evolutionary mechanisms on the genetic make-up of populations.

Population genomic data, without any environmental or phenotypic information, can be used to scan the genomes of weed and non-weed relatives to identify selective sweeps, pointing at loci supporting weed adaptation on micro- or macro-evolutionary scales. Two recent within-species examples include weedy rice, where population differentiation between weedy and domesticated populations was used to identify the genetic basis of weedy de-domestication [ 73 ], and common waterhemp, where consistent allelic differences among natural and agricultural collections resolved a complex set of agriculturally adaptive alleles [ 74 , 75 ]. A recent comparative population genomic study of weedy barnyardgrass and crop millet species has demonstrated how inter-specific investigations can resolve the signatures of crop and weed evolution [ 76 ] (also see [ 77 ] for a non-weed climate adaptation example). Multiple sequence alignments across numerous species provide complementary insight into adaptive convergence over deeper timescales, even with just one genomic sample per species (e.g., [ 78 , 79 ]). Thus, newly sequenced weed genomes combined with genomes available for closely related crops (outlined by [ 14 , 80 ]) and an effort to identify other non-weed wild relatives will be invaluable in characterizing the genetic architecture of weed adaptation and evolution across diverse species.

Weeds experience high levels of genetic selection, both artificial in response to agricultural practices and particularly herbicides, and natural in response to the environmental conditions they encounter [ 81 , 82 ]. Using genomic analysis to identify loci that are the targets of selection, whether natural or artificial, would point at vulnerabilities that could be leveraged against weeds to develop new and more sustainable management strategies [ 83 ]. This is a key motivation to develop genotype-by-environment association (GEA) and selective sweep scan approaches, which allow researchers to resolve the molecular basis of multi-dimensional adaptation [ 84 , 85 ]. GEA approaches, in particular, have been widely used on landscape-wide resequencing collections to determine the genetic basis of climate adaptation (e.g., [ 27 , 86 , 87 ]), but have yet to be fully exploited to diagnose the genetic basis of the various aspects of weediness [ 88 ]. Armed with data on environmental dimensions of agricultural settings, such as focal crop, soil quality, herbicide use, and climate, GEA approaches can help disentangle how discrete farming practices have influenced the evolution of weediness and resolve broader patterns of local adaptation across a weed’s range. Although non-weedy relatives are not technically required for GEA analyses, inclusion of environmental and genomic data from weed progenitors can further distinguish genetic variants underpinning weed origins from those involved in local adaptation.

New weeds emerge frequently [ 89 ], either through hybridization between species as documented for sea beet ( Beta vulgaris ssp. maritima) hybridizing with crop beet to produce progeny that are well adapted to agricultural conditions [ 90 , 91 , 92 ], or through the invasion of alien species that find a new range to colonize. Biosecurity measures are often in place to stop the introduction of new weeds; however, the vast scale of global agricultural commodity trade precludes the possibility of total control. Population genomic analysis is now able to measure gene flow between populations [ 74 , 93 , 94 , 95 ] and identify populations of origin for invasive species including weeds [ 96 , 97 , 98 ]. For example, the invasion route of the pest fruitfly Drosophila suzukii from Eastern Asia to North America and Europe through Hawaii was deciphered using Approximate Bayesian Computation on high-throughput sequencing data from a global sample of multiple populations [ 99 ]. Genomics can also be leveraged to predict invasion rather than explain it. The resequencing of a global sample of common ragweed ( Ambrosia artemisiifolia L.) elucidated a complex invasion route whereby Europe was invaded by multiple introductions of American ragweed that hybridized in Europe prior to a subsequent introduction to Australia [ 100 , 101 ]. In this context, the use of genomically informed species distribution models helps assess the risk associated with different source populations, which in the case of common ragweed, suggests that a source population from Florida would allow ragweed to invade most of northern Australia [ 102 ]. Globally coordinated research efforts to understand potential distribution models could support the transformation of biosecurity from perspective analysis towards predictive risk assessment.

Herbicide resistance and weed management

Herbicide resistance is among the numerous weedy traits that can evolve in plant populations exposed to agricultural selection pressures. Over-reliance on herbicides to control weeds, along with low diversity and lack of redundancy in weed management strategies, has resulted in globally widespread herbicide resistance [ 103 ]. To date, 272 herbicide-resistant weed species have been reported worldwide, and at least one resistance case exists for 21 of the 31 existing herbicide sites of action [ 104 ]—significantly limiting chemical weed control options available to agriculturalists. This limitation of control options is exacerbated by the recent lack of discovery of herbicides with new sites of action [ 105 ].

Herbicide resistance may result from several different physiological mechanisms. Such mechanisms have been classified into two main groups, target-site resistance (TSR) [ 4 , 106 ] and non-target-site resistance (NTSR) [ 4 , 107 ]. The first group encompasses changes that reduce binding affinity between a herbicide and its target [ 108 ]. These changes may provide resistance to multiple herbicides that have a common biochemical target [ 109 ] and can be effectively managed through mixture and/or rotation of herbicides targeting different sites of action [ 110 ]. The second group (NTSR), includes alterations in herbicide absorption, translocation, sequestration, and/or metabolism that may lead to unpredictable pleotropic cross-resistance profiles where structurally and functionally diverse herbicides are rendered ineffective by one or more genetic variant(s) [ 47 ]. This mechanism of resistance threatens not only the efficacy of existing herbicidal chemistries, but also ones yet to be discovered. While TSR is well understood because of the ease of identification and molecular characterization of target site variants, NTSR mechanisms are significantly more challenging to research because they are often polygenic, and the resistance causing element(s) are not well understood [ 111 ].

Improving the current understanding of metabolic NTSR mechanisms is not an easy task, since genes of diverse biochemical functions are involved, many of which exist as extensive gene families [ 109 , 112 ]. Expression changes of NTSR genes have been implicated in several resistance cases where the protein products of the genes are functionally equivalent across sensitive and resistant plants, but their relative abundance leads to resistance. Thus, regulatory elements of NTSR genes have been scrutinized to understand their role in NTSR mechanisms [ 113 ]. Similarly, epigenetic modifications have been hypothesized to play a role in NTSR, with much remaining to be explored [ 114 , 115 , 116 ]. Untargeted approaches such as genome-wide association, selective sweep scans, linkage mapping, RNA-sequencing, and metabolomic profiling have proven helpful to complement more specific biochemical- and chemo-characterization studies towards the elucidation of NTSR mechanisms as well as their regulation and evolution [ 47 , 117 , 118 , 119 , 120 , 121 , 122 , 123 , 124 ]. Even in cases where resistance has been attributed to TSR, genetic mapping approaches can detect other NTSR loci contributing to resistance (as shown by [ 123 ]) and provide further evidence for the role of TSR mutations across populations. Knowledge of the genetic basis of NTSR will aid the rational design of herbicides by screening new compounds for interaction with newly discovered NTSR proteins during early research phases and by identifying conserved chemical structures that interact with these proteins that should be avoided in small molecule design.

Genomic resources can also be used to predict the protein structure for novel herbicide target site and metabolism genes. This will allow for prediction of efficacy and selectivity for new candidate herbicides in silico to increase herbicide discovery throughput as well as aid in the design and development of next-generation technologies for sustainable weed management. Proteolysis targeting chimeras (PROTACs) have the potential to bind desired targets with great selectivity and degrade proteins by utilizing natural protein ubiquitination and degradation pathways within plants [ 125 ]. Spray-induced gene silencing in weeds using oligonucleotides has potential as a new, innovative, and sustainable method for weed management, but improved methods for design and delivery of oligonucleotides are needed to make this technique a viable management option [ 50 ]. Additionally, success in the field of pharmaceutical drug discovery in the development of molecules modulating protein–protein interactions offers another potential avenue towards the development of herbicides with novel targets [ 126 , 127 ]. High-quality reference genomes allow for the design of new weed management technologies like the ones listed here that are specific to—and effective across—weed species but have a null effect on non-target organisms.

Comparative genomics and genome biology

The genomes of weed species are as diverse as weed species themselves. Weeds are found across highly diverged plant families and often have no phylogenetically close model or crop species relatives for comparison. On all measurable metrics, weed genomes run the gamut. Some have smaller genomes like Cyperus spp. (~ 0.26 Gb) while others are larger, such as Avena fatua (~ 11.1 Gb) (Table  1 ). Some have high heterozygosity in terms of single-nucleotide polymorphisms, such as the Amaranthus spp., while others are primarily self-pollinated and quite homozygous, such as Poa annua [ 128 , 129 ]. Some are diploid such as Conyza canadensis and Echinochloa haploclada while others are polyploid such as C. sumetrensis , E. crus-galli , and E. colona [ 76 ]. The availability of genomic resources in these diverse, unexplored branches of the tree of life allows us to identify consistencies and anomalies in the field of genome biology.

The weed genomes published so far have focused mainly on weeds of agronomic crops, and studies have revolved around their ability to resist key herbicides. For example, genomic resources were vital in the elucidation of herbicide resistance cases involving target site gene copy number variants (CNVs). Gene CNVs of 5-enolpyruvylshikimate-3-phosphate synthase ( EPSPS ) have been found to confer resistance to the herbicide glyphosate in diverse weed species. To date, nine species have independently evolved EPSPS CNVs, and species achieve increased EPSPS copy number via different mechanisms [ 153 ]. For instance, the EPSPS CNV in Bassia scoparia is caused by tandem duplication, which is accredited to transposable element insertions flanking EPSPS and subsequent unequal crossing over events [ 154 , 155 ]. In Eleusine indica , a EPSPS CNV was caused by translocation of the EPSPS locus into the subtelomere followed by telomeric sequence exchange [ 156 ]. One of the most fascinating genome biology discoveries in weed science has been that of extra-chromosomal circular DNAs (eccDNAs) that harbor the EPSPS gene in the weed species Amaranthus palmeri [ 157 , 158 ]. In this case, the eccDNAs autonomously replicate separately from the nuclear genome and do not reintegrate into chromosomes, which has implications for inheritance, fitness, and genome structure [ 159 ]. These discoveries would not have been possible without reference assemblies of weed genomes, next-generation sequencing, and collaboration with experts in plant genomics and bioinformatics.

Another question that is often explored with weedy genomes is the nature and composition of gene families that are associated with NTSR. Gene families under consideration often include cytochrome P450s (CYPs), glutathione- S -transferases (GSTs), ABC transporters, etc. Some questions commonly considered with new weed genomes include how many genes are in each of these gene families, where are they located, and which weed accessions and species have an over-abundance of them that might explain their ability to evolve resistance so rapidly [ 76 , 146 , 160 , 161 ]? Weed genome resources are necessary to answer questions about gene family expansion or contraction during the evolution of weediness, including the role of polyploidy in NTSR gene family expansion as explored by [ 162 ].

Translational research and communication with weed management stakeholders

Whereas genomics of model plants is typically aimed at addressing fundamental questions in plant biology, and genomics of crop species has the obvious goal of crop improvement, goals of genomics of weedy plants also include the development of more effective and sustainable strategies for their management. Weed genomic resources assist with these objectives by providing novel molecular ecological and evolutionary insights from the context of intensive anthropogenic management (which is lacking in model plants), and offer knowledge and resources for trait discovery for crop improvement, especially given that many wild crop relatives are also important agronomic weeds (e.g., [ 163 ]). For instance, crop-wild relatives are valuable for improving crop breeding for marginal environments [ 164 ]. Thus, weed genomics presents unique opportunities and challenges relative to plant genomics more broadly. It should also be noted that although weed science at its core is an applied discipline, it draws broadly from many scientific disciplines such as, plant physiology, chemistry, ecology, and evolutionary biology, to name a few. The successful integration of weed-management strategies, therefore, requires extensive collaboration among individuals collectively possessing the necessary expertise [ 165 ].

With the growing complexity of herbicide resistance management, practitioners are beginning to recognize the importance of understanding resistance mechanisms to inform appropriate management tactics [ 14 ]. Although weed science practitioners do not need to understand the technical details of weed genomics, their appreciation of the power of weed genomics—together with their unique insights from field observations—will yield novel opportunities for applications of weed genomics to weed management. In particular, combining field management history with information on weed resistance mechanisms is expected to provide novel insights into evolutionary trajectories (e.g. [ 6 , 166 ]), which can be utilized for disrupting evolutionary adaptation. It can be difficult to obtain field history information from practitioners, but developing an understanding among them of the importance of such information can be invaluable.

Development of weed genomics resources by the IWGC

Weed genomics is a fast-growing field of research with many recent breakthroughs and many unexplored areas of study. The International Weed Genomics Consortium (IWGC) started in 2021 to address the roadblocks listed above and to promote the study of weedy plants. The IWGC is an open collaboration among academic, government, and industry researchers focused on producing genomic tools for weedy species from around the world. Through this collaboration, our initial aim is to provide chromosome-level reference genome assemblies for at least 50 important weedy species from across the globe that are chosen based on member input, economic impact, and global prevalence (Fig.  1 ). Each genome will include annotation of gene models and repetitive elements and will be freely available through public databases with no intellectual property restrictions. Additionally, future funding of the IWGC will focus on improving gene annotations and supplementing these reference genomes with tools that increase their utility.

figure 1

The International Weed Genomics Consortium (IWGC) collected input from the weed genomics community to develop plans for weed genome sequencing, annotation, user-friendly genome analysis tools, and community engagement

Reference genomes and data analysis tools

The first objective of the IWGC is to provide high-quality genomic resources for agriculturally important weeds. The IWGC therefore created two main resources for information about, access to, or analysis of weed genomic data (Fig.  1 ). The IWGC website (available at [ 167 ]) communicates the status and results of genome sequencing projects, information on training and funding opportunities, upcoming events, and news in weed genomics. It also contains details of all sequenced species including genome size, ploidy, chromosome number, herbicide resistance status, and reference genome assembly statistics. The IWGC either compiles existing data on genome size, ploidy, and chromosome number, or obtains the data using flow cytometry and cytogenetics (Fig.  1 ; Additional File 2 : Fig S1-S4). Through this website, users can request an account to access our second main resource, an online genome database called WeedPedia (accessible at [ 168 ]), with an account that is created within 3–5 working days of an account request submission. WeedPedia hosts IWGC-generated and other relevant publicly accessible genomic data as well as a suite of bioinformatic tools. Unlike what is available for other fields, weed science did not have a centralized hub for genomics information, data, and analysis prior to the IWGC. Our intention in creating WeedPedia is to encourage collaboration and equity of access to information across the research community. Importantly, all genome assemblies and annotations from the IWGC (Table  1 ), along with the raw data used to produce them, will be made available through NCBI GenBank. Upon completion of a 1-year sponsoring member data confidentiality period for each species (dates listed in Table  1 ), scientific teams within the IWGC produce the first genome-wide investigation to submit for publication including whole genome level analyses on genes, gene families, and repetitive sequences as well as comparative analysis with other species. Genome assemblies and data will be publicly available through NCBI as part of these initial publications for each species.

WeedPedia is a cloud-based omics database management platform built from the software “CropPedia” and licensed from KeyGene (Wageningen, The Netherlands). The interface allows users to access, visualize, and download genome assemblies along with structural and functional annotation. The platform includes a genome browser, comparative map viewer, pangenome tools, RNA-sequencing data visualization tools, genetic mapping and marker analysis tools, and alignment capabilities that allow searches by keyword or sequence. Additionally, genes encoding known target sites of herbicides have been specially annotated, allowing users to quickly identify and compare these genes of interest. The platform is flexible, making it compatible with future integration of other data types such as epigenetic or proteomic information. As an online platform with a graphical user interface, WeedPedia provides user-friendly, intuitive tools that encourage users to integrate genomics into their research while also allowing more advanced users to download genomic data to be used in custom analysis pipelines. We aspire for WeedPedia to mimic the success of other public genomic databases such as NCBI, CoGe, Phytozome, InsectBase, and Mycocosm to name a few. WeedPedia currently hosts reference genomes for 40 species (some of which are currently in their 1-year confidentiality period) with additional genomes in the pipeline to reach a currently planned total of 55 species (Table  1 ). These genomes include both de novo reference genomes generated or in progress by the IWGC (31 species; Table  1 ), and publicly available genome assemblies of 24 weedy or related species that were generated by independent research groups (Table  2 ). As of May 2024, WeedPedia has over 370 registered users from more than 27 countries spread across 6 continents.

The IWGC reference genomes are generated in partnership with the Corteva Agriscience Genome Center of Excellence (Johnston, Iowa) using a combination of single-molecule long-read sequencing, optical genome maps, and chromosome conformation mapping. This strategy has already yielded highly contiguous, phased, chromosome-level assemblies for 26 weed species, with additional assemblies currently in progress (Table  1 ). The IWGC assemblies have been completed as single or haplotype-resolved double-haplotype pseudomolecules in inbreeding and outbreeding species, respectively, with multiple genomes being near gapless. For example, the de novo assemblies of the allohexaploids Conyza sumatrensis and Chenopodium album have all chromosomes captured in single scaffolds and most chromosomes being gapless from telomere to telomere. Complementary full-length isoform (IsoSeq) sequencing of RNA collected from diverse tissue types and developmental stages assists in the development of gene models during annotation.

As with accessibility of data, a core objective of the IWGC is to facilitate open access to sequenced germplasm when possible for featured species. Historically, the weed science community has rarely shared or adopted standard germplasm (e.g., specific weed accessions). The IWGC has selected a specific accession of each species for reference genome assembly (typically susceptible to herbicides). In collaboration with a parallel effort by the Herbicide Resistant Plants committee of the Weed Science Society of America, seeds of the sequenced weed accessions will be deposited in the United States Department of Agriculture Germplasm Resources Information Network [ 186 ] for broad access by the scientific community and their accession numbers will be listed on the IWGC website. In some cases, it is not possible to generate enough seed to deposit into a public repository (e.g., plants that typically reproduce vegetatively, that are self-incompatible, or that produce very few seeds from a single individual). In these cases, the location of collection for sequenced accessions will at least inform the community where the sequenced individual came from and where they may expect to collect individuals with similar genotypes. The IWGC ensures that sequenced accessions are collected and documented to comply with the Nagoya Protocol on access to genetic resources and the fair and equitable sharing of benefits arising from their utilization under the Convention on Biological Diversity and related Access and Benefit Sharing Legislation [ 187 ]. As additional accessions of weed species are sequenced (e.g., pangenomes are obtained), the IWGC will facilitate germplasm sharing protocols to support collaboration. Further, to simplify the investigation of herbicide resistance, the IWGC will link WeedPedia with the International Herbicide-Resistant Weed Database [ 104 ], an already widely known and utilized database for weed scientists.

Training and collaboration in weed genomics

Beyond producing genomic tools and resources, a priority of the IWGC is to enable the utilization of these resources across a wide range of stakeholders. A holistic approach to training is required for weed science generally [ 188 ], and we would argue even more so for weed genomics. To accomplish our training goals, the IWGC is developing and delivering programs aimed at the full range of IWGC stakeholders and covering a breadth of relevant topics. We have taken care to ensure our approaches are diverse as to provide training to researchers with all levels of existing experience and differing reasons for engaging with these tools. Throughout, the focus is on ensuring that our training and outreach result in impacts that benefit a wide range of stakeholders.

Although recently developed tools are incredibly enabling and have great potential to replace antiquated methodology [ 189 ] and to solve pressing weed science problems [ 14 ], specialized computational skills are required to fully explore and unlock meaning from these highly complex datasets. Collaboration with, or training of, computational biologists equipped with these skills and resources developed by the IWGC will enable weed scientists to expand research programs and better understand the genetic underpinnings of weed evolution and herbicide resistance. To fill existing skill gaps, the IWGC is developing summer bootcamps and online modules directed specifically at weed scientists that will provide training on computational skills (Fig.  1 ). Because successful utilization of the IWGC resources requires more than general computational skills, we have created three targeted workshops that teach practical skills related to genomics databases, molecular biology, and population genomics (available at [ 190 ]). The IWGC has also hosted two official conference meetings, one in September of 2021 and one in January of 2023, with more conferences planned. These conferences have included invited speakers to present successful implementations of weed genomics, educational workshops to build computational skills, and networking opportunities for research to connect and collaborate.

Engagement opportunities during undergraduate degrees have been shown to improve academic outcomes [ 191 , 192 ]. As one activity to help achieve this goal, the IWGC has sponsored opportunities for US undergraduates to undertake a 10-week research experience, which includes an introduction to bioinformatics, a plant genomics research project that results in a presentation, and access to career building opportunities in diverse workplace environments. To increase equitable access to conferences and professional communities, we supported early career researchers to attend the first two IWGC conferences in the USA as well as workshops and bootcamps in Europe, South America, and Australia. These hybrid or in-person travel grants are intentionally designed to remove barriers and increase participation of individuals from backgrounds and experiences currently underrepresented within weed/plant science or genomics [ 193 ]. Recipients of these travel awards gave presentations and gained the measurable benefits that come from either virtual or in-person participation in conferences [ 194 ]. Moving forward, weed scientists must amass skills associated with genomic analyses and collaborate with other area experts to fully leverage resources developed by the IWGC.

The tools generated through the IWGC will enable many new research projects with diverse objectives like those listed above. In summary, contiguous genome assemblies and complete annotation information will allow weed scientists to join plant breeders in the use of genetic mapping for many traits including stress tolerance, plant architecture, and herbicide resistance (especially important for cases of NTSR). These assemblies will also allow for investigations of population structure, gene flow, and responses to evolutionary mechanisms like genetic bottlenecking and artificial selection. Understanding gene sequences across diverse weed species will be vital in modeling new herbicide target site proteins and designing novel effective herbicides with minimal off-target effects. The IWGC website will improve accessibility to weed genomics data by providing a single hub for reference genomes as well as phenotypic and genotypic information for accessions shared with the IWGC. Deposition of sequenced germplasm into public repositories will ensure that researchers are able to access and utilize these accessions in their own research to make the field more standardized and equitable. WeedPedia allows users of all backgrounds to quickly access information of interest such as herbicide target site gene sequence or subcellular localization of protein products for different genes. Users can also utilize server-based tools such as BLAST and genome browsing similar to other public genomic databases. Finally, the IWGC is committed to training and connecting weed genomicists through hosting trainings, workshops, and conferences.

Conclusions

Weeds are unique and fascinating plants, having significant impacts on agriculture and ecosystems; and yet, aspects of their biology, ecology, and genetics remain poorly understood. Weeds represent a unique area within plant biology, given their repeated rapid adaptation to sudden and severe shifts in the selective landscape of anthropogenic management practices. The production of a public genomics database with reference genomes and annotations for over 50 weed species represents a substantial step forward towards research goals that improve our understanding of the biology and evolution of weeds. Future work is needed to improve annotations, particularly for complex gene families involved in herbicide detoxification, structural variants, and mobile genetic elements. As reference genome assemblies become available; standard, affordable methods for gathering genotype information will allow for the identification of genetic variants underlying traits of interest. Further, methods for functional validation and hypothesis testing are needed in weeds to validate the effect of genetic variants detected through such experiments, including systems for transformation, gene editing, and transient gene silencing and expression. Future research should focus on utilizing weed genomes to investigate questions about evolutionary biology, ecology, genetics of weedy traits, and weed population dynamics. The IWGC plans to continue the public–private partnership model to host the WeedPedia database over time, integrate new datasets such as genome resequencing and transcriptomes, conduct trainings, and serve as a research coordination network to ensure that advances in weed science from around the world are shared across the research community (Fig.  1 ). Bridging basic plant genomics with translational applications in weeds is needed to deliver on the potential of weed genomics to improve weed management and crop breeding.

Availability of data and materials

All genome assemblies and related sequencing data produced by the IWGC will be available through NCBI as part of publications reporting the first genome-wide analysis for each species.

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Peer review information

Wenjing She was the primary editor of this article and managed its editorial process and peer review in collaboration with the rest of the editorial team.

The International Weed Genomics Consortium is supported by BASF SE, Bayer AG, Syngenta Ltd, Corteva Agriscience, CropLife International (Global Herbicide Resistance Action Committee), the Foundation for Food and Agriculture Research (Award DSnew-0000000024), and two conference grants from USDA-NIFA (Award numbers 2021–67013-33570 and 2023-67013-38785).

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Department of Agricultural Biology, Colorado State University, 1177 Campus Delivery, Fort Collins, CO, 80523, USA

Jacob Montgomery, Sarah Morran & Todd A. Gaines

Protecting Crops and the Environment, Rothamsted Research, Harpenden, Hertfordshire, UK

Dana R. MacGregor

Department of Crop, Soil, and Environmental Sciences, Auburn University, Auburn, AL, USA

J. Scott McElroy

Department of Plant and Environmental Sciences, University of Copenhagen, Taastrup, Denmark

Paul Neve & Célia Neto

IFEVA-Conicet-Department of Ecology, University of Buenos Aires, Buenos Aires, Argentina

Martin M. Vila-Aiub & Maria Victoria Sandoval

Department of Ecology, Faculty of Agronomy, University of Buenos Aires, Buenos Aires, Argentina

Analia I. Menéndez

Department of Botany, The University of British Columbia, Vancouver, BC, Canada

Julia M. Kreiner

Institute of Crop Sciences, Zhejiang University, Hangzhou, China

Longjiang Fan

Department of Biology, University of Massachusetts Amherst, Amherst, MA, USA

Ana L. Caicedo

Department of Plant and Wildlife Sciences, Brigham Young University, Provo, UT, USA

Peter J. Maughan

Bayer AG, Weed Control Research, Frankfurt, Germany

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Department of Crop Sciences, Federal University of Rio Grande Do Sul, Porto Alegre, Rio Grande Do Sul, Brazil

Aldo Merotto Jr.

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Contributions

JMo and TG conceived and outlined the article. TG, DM, EP, RB, JSM, PJT, MJ wrote grants to obtain funding. MMI, BSG, and MJ performed mitotic chromosome visualization. VL performed sequencing. VL and KF assembled the genomes. LC and ELP annotated the genomes. JMo, SM, DRM, JSM, PN, CN, MV, MVS, AIM, JMK, LF, ALC, PJM, BABM, JMi, AC, MVB, LC, AFL, and ELP wrote the first draft of the article. All authors edited the article and improved the final version.

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Correspondence to Todd A. Gaines .

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Some authors work for commercial agricultural companies (BASF, Bayer, Corteva Agriscience, or Syngenta) that develop and sell weed control products.

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Supplementary Information

13059_2024_3274_moesm1_esm.docx.

Additional file 1. List of completed and in-progress genome assemblies of weed species pollinated by insects (Table S1).

13059_2024_3274_MOESM2_ESM.docx

Additional file 2. Methods and results for visualizing and counting the metaphase chromosomes of hexaploid Avena fatua (Fig S1); diploid Lolium rigidum  (Fig S2); tetraploid Phalaris minor (Fig S3); and tetraploid Salsola tragus (Fig S4).

Additional file 3. Review history.

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Montgomery, J., Morran, S., MacGregor, D.R. et al. Current status of community resources and priorities for weed genomics research. Genome Biol 25 , 139 (2024). https://doi.org/10.1186/s13059-024-03274-y

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DOI : https://doi.org/10.1186/s13059-024-03274-y

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  1. Null & Alternative Hypotheses

    Revised on June 22, 2023. The null and alternative hypotheses are two competing claims that researchers weigh evidence for and against using a statistical test: Null hypothesis (H0): There's no effect in the population. Alternative hypothesis (Ha or H1): There's an effect in the population. The effect is usually the effect of the ...

  2. Null and Alternative Hypotheses

    The null and alternative hypotheses offer competing answers to your research question. When the research question asks "Does the independent variable affect the dependent variable?", the null hypothesis (H 0) answers "No, there's no effect in the population.". On the other hand, the alternative hypothesis (H A) answers "Yes, there ...

  3. Null Hypothesis: Definition, Rejecting & Examples

    The null hypothesis in statistics states that there is no difference between groups or no relationship between variables. It is one of two mutually exclusive hypotheses about a population in a hypothesis test. When your sample contains sufficient evidence, you can reject the null and conclude that the effect is statistically significant.

  4. Null hypothesis

    In scientific research, the null hypothesis (often denoted H 0) is the claim that the effect being studied does not exist. The null hypothesis can also be described as the hypothesis in which no relationship exists between two sets of data or variables being analyzed. If the null hypothesis is true, any experimentally observed effect is due to ...

  5. 9.1 Null and Alternative Hypotheses

    The actual test begins by considering two hypotheses.They are called the null hypothesis and the alternative hypothesis.These hypotheses contain opposing viewpoints. H 0, the —null hypothesis: a statement of no difference between sample means or proportions or no difference between a sample mean or proportion and a population mean or proportion. In other words, the difference equals 0.

  6. Null and Alternative Hypotheses

    H 0 always has a symbol with an equal in it. H a never has a symbol with an equal in it. The choice of symbol depends on the wording of the hypothesis test. However, be aware that many researchers (including one of the co-authors in research work) use = in the null hypothesis, even with > or < as the symbol in the alternative hypothesis.

  7. 7.3: The Research Hypothesis and the Null Hypothesis

    The Research Hypothesis. A research hypothesis is a mathematical way of stating a research question. A research hypothesis names the groups (we'll start with a sample and a population), what was measured, and which we think will have a higher mean. The last one gives the research hypothesis a direction. In other words, a research hypothesis ...

  8. An Introduction to Statistics: Understanding Hypothesis Testing and

    HYPOTHESIS TESTING. A clinical trial begins with an assumption or belief, and then proceeds to either prove or disprove this assumption. In statistical terms, this belief or assumption is known as a hypothesis. Counterintuitively, what the researcher believes in (or is trying to prove) is called the "alternate" hypothesis, and the opposite ...

  9. How to Write a Strong Hypothesis

    6. Write a null hypothesis. If your research involves statistical hypothesis testing, you will also have to write a null hypothesis. The null hypothesis is the default position that there is no association between the variables. The null hypothesis is written as H 0, while the alternative hypothesis is H 1 or H a.

  10. 9.1: Null and Alternative Hypotheses

    The actual test begins by considering two hypotheses.They are called the null hypothesis and the alternative hypothesis.These hypotheses contain opposing viewpoints. \(H_0\): The null hypothesis: It is a statement of no difference between the variables—they are not related. This can often be considered the status quo and as a result if you cannot accept the null it requires some action.

  11. How to Write a Null Hypothesis (5 Examples)

    Whenever we perform a hypothesis test, we always write a null hypothesis and an alternative hypothesis, which take the following forms: H0 (Null Hypothesis): Population parameter =, ≤, ≥ some value. HA (Alternative Hypothesis): Population parameter <, >, ≠ some value. Note that the null hypothesis always contains the equal sign.

  12. Null Hypothesis Definition and Examples

    Null Hypothesis Examples. "Hyperactivity is unrelated to eating sugar " is an example of a null hypothesis. If the hypothesis is tested and found to be false, using statistics, then a connection between hyperactivity and sugar ingestion may be indicated. A significance test is the most common statistical test used to establish confidence in a ...

  13. How to Formulate a Null Hypothesis (With Examples)

    To distinguish it from other hypotheses, the null hypothesis is written as H 0 (which is read as "H-nought," "H-null," or "H-zero"). A significance test is used to determine the likelihood that the results supporting the null hypothesis are not due to chance. A confidence level of 95% or 99% is common. Keep in mind, even if the confidence level is high, there is still a small chance the ...

  14. A Practical Guide to Writing Quantitative and Qualitative Research

    On the other hand, a research hypothesis is an educated statement of an expected outcome. ... - Following a null hypothesis, an alternative hypothesis predicts a relationship between 2 study variables: The new drug (variable 1) is better on average in reducing the level of pain from pulmonary metastasis than the current drug (variable 2). ...

  15. Null Hypothesis Definition and Examples, How to State

    Step 1: Figure out the hypothesis from the problem. The hypothesis is usually hidden in a word problem, and is sometimes a statement of what you expect to happen in the experiment. The hypothesis in the above question is "I expect the average recovery period to be greater than 8.2 weeks.". Step 2: Convert the hypothesis to math.

  16. Null Hypothesis

    Definition. In formal hypothesis testing, the null hypothesis ( H0) is the hypothesis assumed to be true in the population and which gives rise to the sampling distribution of the test statistic in question (Hays 1994 ). The critical feature of the null hypothesis across hypothesis testing frameworks is that it is stated with enough precision ...

  17. What is Null Hypothesis? What Is Its Importance in Research?

    Scientists begin their research with a hypothesis that a relationship of some kind exists between variables. The null hypothesis is the opposite stating that no such relationship exists. Null hypothesis may seem unexciting, but it is a very important aspect of research. In this article, we discuss what null hypothesis is, how to make use of it ...

  18. Examples of null and alternative hypotheses

    The null hypothesis is what happens at baseline. It is the uninteresting hypothesis--the boring hypothesis. Usually, it is the hypothesis that assumes no difference. It is the opposite of your research hypothesis. The alternative hypothesis--that is, the research hypothesis--is the idea, phenomenon, observation that you want to prove.

  19. Null & Alternative Hypotheses

    The null hypothesis is a presumption of status quo or no change. Alternative Hypothesis (H a) - This is also known as the claim. This hypothesis should state what you expect the data to show, based on your research on the topic. This is your answer to your research question. Examples: Null Hypothesis: H 0: There is no difference in the salary ...

  20. Understanding Null Hypothesis Testing

    A crucial step in null hypothesis testing is finding the likelihood of the sample result if the null hypothesis were true. This probability is called the p value. A low p value means that the sample result would be unlikely if the null hypothesis were true and leads to the rejection of the null hypothesis. A high p value means that the sample ...

  21. Research Hypothesis In Psychology: Types, & Examples

    A research hypothesis, in its plural form "hypotheses," is a specific, testable prediction about the anticipated results of a study, established at its outset. ... The null hypothesis, positing no effect or relationship, is a foundational contrast to the research hypothesis in scientific inquiry. It establishes a baseline for statistical ...

  22. 9.1 Null and Alternative Hypotheses

    The actual test begins by considering two hypotheses.They are called the null hypothesis and the alternative hypothesis.These hypotheses contain opposing viewpoints. H 0: The null hypothesis: It is a statement of no difference between the variables—they are not related. This can often be considered the status quo and as a result if you cannot accept the null it requires some action.

  23. Why we habitually engage in null-hypothesis significance testing: A

    Null Hypothesis Significance Testing (NHST) is the most familiar statistical procedure for making inferences about population effects. ... These alternatives build on the idea that research usually starts with a more informed research-question than one merely assuming the null hypothesis of no effect. These methods overcome the problem of ...

  24. 5 Tips for Interpreting P-Values Correctly in Hypothesis Testing

    In hypothesis testing, the p-value is defined as the probability of observing your data, or data more extreme, if the null hypothesis is true. As a reminder, the null hypothesis states no difference between your data and the expected population. For example, in a hypothesis test to see if changing a company's logo drives more traffic to the ...

  25. Knowledge, attitudes, and practices of primary healthcare practitioners

    To date, most research on pharmacist clinics comes from countries like the United States, the UK, Canada, ... In case of rejection of the null hypothesis, multiple pairwise comparisons would be conducted as confirmatory post hoc analysis using Bonferroni correction. Based on the univariate analysis results, we constructed binary logistic ...

  26. Current status of community resources and priorities for weed genomics

    Weeds are attractive models for basic and applied research due to their impacts on agricultural systems and capacity to swiftly adapt in response to anthropogenic selection pressures. Currently, a lack of genomic information precludes research to elucidate the genetic basis of rapid adaptation for important traits like herbicide resistance and stress tolerance and the effect of evolutionary ...