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Null & Alternative Hypotheses | Definitions, Templates & Examples

Published on May 6, 2022 by Shaun Turney . 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 ( H 0 ): There’s no effect in the population .
• Alternative hypothesis ( H a or H 1 ) : There’s an effect in the population.

Table of contents

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

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.”
• 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. It’s critical for your research to write strong hypotheses .

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.

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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 ≤).

You can never know with complete certainty whether there is an effect in the population. Some percentage of the time, your inference about the population will be incorrect. When you incorrectly reject the null hypothesis, it’s called a type I error . When you incorrectly fail to reject it, it’s a type II error.

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.

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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.

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 template sentences

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.

If you want to know more about statistics , methodology , or research bias , make sure to check out some of our other articles with explanations and examples.

• Normal distribution
• Descriptive statistics
• Measures of central tendency
• Correlation coefficient

Methodology

• Cluster sampling
• Stratified sampling
• Types of interviews
• Cohort study
• Thematic analysis

Research bias

• Implicit bias
• Cognitive bias
• Survivorship bias
• Availability heuristic
• Nonresponse bias
• Regression to the mean

Hypothesis testing is a formal procedure for investigating our ideas about the world using statistics. It is used by scientists to test specific predictions, called hypotheses , by calculating how likely it is that a pattern or relationship between variables could have arisen by chance.

Null and alternative hypotheses are used in statistical hypothesis testing . The null hypothesis of a test always predicts no effect or no relationship between variables, while the alternative hypothesis states your research prediction of an effect or relationship.

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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1 1 Slide © 2008 Thomson South-Western. All Rights Reserved Slides by JOHN LOUCKS St. Edward’s University.

1 Chapter 9 Hypothesis Testing Developing Null and Alternative Hypotheses Type I and Type II Errors One-Tailed Tests About a Population Mean: Large-Sample.

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Null hypothesis significance testing: a short tutorial

Cyril pernet.

1 Centre for Clinical Brain Sciences (CCBS), Neuroimaging Sciences, The University of Edinburgh, Edinburgh, UK

Version Changes

Revised. amendments from version 2.

This v3 includes minor changes that reflect the 3rd reviewers' comments - in particular the theoretical vs. practical difference between Fisher and Neyman-Pearson. Additional information and reference is also included regarding the interpretation of p-value for low powered studies.

Peer Review Summary

Although thoroughly criticized, null hypothesis significance testing (NHST) remains the statistical method of choice used to provide evidence for an effect, in biological, biomedical and social sciences. In this short tutorial, I first summarize the concepts behind the method, distinguishing test of significance (Fisher) and test of acceptance (Newman-Pearson) and point to common interpretation errors regarding the p-value. I then present the related concepts of confidence intervals and again point to common interpretation errors. Finally, I discuss what should be reported in which context. The goal is to clarify concepts to avoid interpretation errors and propose reporting practices.

The Null Hypothesis Significance Testing framework

NHST is a method of statistical inference by which an experimental factor is tested against a hypothesis of no effect or no relationship based on a given observation. The method is a combination of the concepts of significance testing developed by Fisher in 1925 and of acceptance based on critical rejection regions developed by Neyman & Pearson in 1928 . In the following I am first presenting each approach, highlighting the key differences and common misconceptions that result from their combination into the NHST framework (for a more mathematical comparison, along with the Bayesian method, see Christensen, 2005 ). I next present the related concept of confidence intervals. I finish by discussing practical aspects in using NHST and reporting practice.

Fisher, significance testing, and the p-value

The method developed by ( Fisher, 1934 ; Fisher, 1955 ; Fisher, 1959 ) allows to compute the probability of observing a result at least as extreme as a test statistic (e.g. t value), assuming the null hypothesis of no effect is true. This probability or p-value reflects (1) the conditional probability of achieving the observed outcome or larger: p(Obs≥t|H0), and (2) is therefore a cumulative probability rather than a point estimate. It is equal to the area under the null probability distribution curve from the observed test statistic to the tail of the null distribution ( Turkheimer et al. , 2004 ). The approach proposed is of ‘proof by contradiction’ ( Christensen, 2005 ), we pose the null model and test if data conform to it.

In practice, it is recommended to set a level of significance (a theoretical p-value) that acts as a reference point to identify significant results, that is to identify results that differ from the null-hypothesis of no effect. Fisher recommended using p=0.05 to judge whether an effect is significant or not as it is roughly two standard deviations away from the mean for the normal distribution ( Fisher, 1934 page 45: ‘The value for which p=.05, or 1 in 20, is 1.96 or nearly 2; it is convenient to take this point as a limit in judging whether a deviation is to be considered significant or not’). A key aspect of Fishers’ theory is that only the null-hypothesis is tested, and therefore p-values are meant to be used in a graded manner to decide whether the evidence is worth additional investigation and/or replication ( Fisher, 1971 page 13: ‘it is open to the experimenter to be more or less exacting in respect of the smallness of the probability he would require […]’ and ‘no isolated experiment, however significant in itself, can suffice for the experimental demonstration of any natural phenomenon’). How small the level of significance is, is thus left to researchers.

What is not a p-value? Common mistakes

The p-value is not an indication of the strength or magnitude of an effect . Any interpretation of the p-value in relation to the effect under study (strength, reliability, probability) is wrong, since p-values are conditioned on H0. In addition, while p-values are randomly distributed (if all the assumptions of the test are met) when there is no effect, their distribution depends of both the population effect size and the number of participants, making impossible to infer strength of effect from them.

Similarly, 1-p is not the probability to replicate an effect . Often, a small value of p is considered to mean a strong likelihood of getting the same results on another try, but again this cannot be obtained because the p-value is not informative on the effect itself ( Miller, 2009 ). Because the p-value depends on the number of subjects, it can only be used in high powered studies to interpret results. In low powered studies (typically small number of subjects), the p-value has a large variance across repeated samples, making it unreliable to estimate replication ( Halsey et al. , 2015 ).

A (small) p-value is not an indication favouring a given hypothesis . Because a low p-value only indicates a misfit of the null hypothesis to the data, it cannot be taken as evidence in favour of a specific alternative hypothesis more than any other possible alternatives such as measurement error and selection bias ( Gelman, 2013 ). Some authors have even argued that the more (a priori) implausible the alternative hypothesis, the greater the chance that a finding is a false alarm ( Krzywinski & Altman, 2013 ; Nuzzo, 2014 ).

The p-value is not the probability of the null hypothesis p(H0), of being true, ( Krzywinski & Altman, 2013 ). This common misconception arises from a confusion between the probability of an observation given the null p(Obs≥t|H0) and the probability of the null given an observation p(H0|Obs≥t) that is then taken as an indication for p(H0) (see Nickerson, 2000 ).

Neyman-Pearson, hypothesis testing, and the α-value

Neyman & Pearson (1933) proposed a framework of statistical inference for applied decision making and quality control. In such framework, two hypotheses are proposed: the null hypothesis of no effect and the alternative hypothesis of an effect, along with a control of the long run probabilities of making errors. The first key concept in this approach, is the establishment of an alternative hypothesis along with an a priori effect size. This differs markedly from Fisher who proposed a general approach for scientific inference conditioned on the null hypothesis only. The second key concept is the control of error rates . Neyman & Pearson (1928) introduced the notion of critical intervals, therefore dichotomizing the space of possible observations into correct vs. incorrect zones. This dichotomization allows distinguishing correct results (rejecting H0 when there is an effect and not rejecting H0 when there is no effect) from errors (rejecting H0 when there is no effect, the type I error, and not rejecting H0 when there is an effect, the type II error). In this context, alpha is the probability of committing a Type I error in the long run. Alternatively, Beta is the probability of committing a Type II error in the long run.

The (theoretical) difference in terms of hypothesis testing between Fisher and Neyman-Pearson is illustrated on Figure 1 . In the 1 st case, we choose a level of significance for observed data of 5%, and compute the p-value. If the p-value is below the level of significance, it is used to reject H0. In the 2 nd case, we set a critical interval based on the a priori effect size and error rates. If an observed statistic value is below and above the critical values (the bounds of the confidence region), it is deemed significantly different from H0. In the NHST framework, the level of significance is (in practice) assimilated to the alpha level, which appears as a simple decision rule: if the p-value is less or equal to alpha, the null is rejected. It is however a common mistake to assimilate these two concepts. The level of significance set for a given sample is not the same as the frequency of acceptance alpha found on repeated sampling because alpha (a point estimate) is meant to reflect the long run probability whilst the p-value (a cumulative estimate) reflects the current probability ( Fisher, 1955 ; Hubbard & Bayarri, 2003 ).

The figure was prepared with G-power for a one-sided one-sample t-test, with a sample size of 32 subjects, an effect size of 0.45, and error rates alpha=0.049 and beta=0.80. In Fisher’s procedure, only the nil-hypothesis is posed, and the observed p-value is compared to an a priori level of significance. If the observed p-value is below this level (here p=0.05), one rejects H0. In Neyman-Pearson’s procedure, the null and alternative hypotheses are specified along with an a priori level of acceptance. If the observed statistical value is outside the critical region (here [-∞ +1.69]), one rejects H0.

Acceptance or rejection of H0?

The acceptance level α can also be viewed as the maximum probability that a test statistic falls into the rejection region when the null hypothesis is true ( Johnson, 2013 ). Therefore, one can only reject the null hypothesis if the test statistics falls into the critical region(s), or fail to reject this hypothesis. In the latter case, all we can say is that no significant effect was observed, but one cannot conclude that the null hypothesis is true. This is another common mistake in using NHST: there is a profound difference between accepting the null hypothesis and simply failing to reject it ( Killeen, 2005 ). By failing to reject, we simply continue to assume that H0 is true, which implies that one cannot argue against a theory from a non-significant result (absence of evidence is not evidence of absence). To accept the null hypothesis, tests of equivalence ( Walker & Nowacki, 2011 ) or Bayesian approaches ( Dienes, 2014 ; Kruschke, 2011 ) must be used.

Confidence intervals

Confidence intervals (CI) are builds that fail to cover the true value at a rate of alpha, the Type I error rate ( Morey & Rouder, 2011 ) and therefore indicate if observed values can be rejected by a (two tailed) test with a given alpha. CI have been advocated as alternatives to p-values because (i) they allow judging the statistical significance and (ii) provide estimates of effect size. Assuming the CI (a)symmetry and width are correct (but see Wilcox, 2012 ), they also give some indication about the likelihood that a similar value can be observed in future studies. For future studies of the same sample size, 95% CI give about 83% chance of replication success ( Cumming & Maillardet, 2006 ). If sample sizes however differ between studies, CI do not however warranty any a priori coverage.

Although CI provide more information, they are not less subject to interpretation errors (see Savalei & Dunn, 2015 for a review). The most common mistake is to interpret CI as the probability that a parameter (e.g. the population mean) will fall in that interval X% of the time. The correct interpretation is that, for repeated measurements with the same sample sizes, taken from the same population, X% of times the CI obtained will contain the true parameter value ( Tan & Tan, 2010 ). The alpha value has the same interpretation as testing against H0, i.e. we accept that 1-alpha CI are wrong in alpha percent of the times in the long run. This implies that CI do not allow to make strong statements about the parameter of interest (e.g. the mean difference) or about H1 ( Hoekstra et al. , 2014 ). To make a statement about the probability of a parameter of interest (e.g. the probability of the mean), Bayesian intervals must be used.

The (correct) use of NHST

NHST has always been criticized, and yet is still used every day in scientific reports ( Nickerson, 2000 ). One question to ask oneself is what is the goal of a scientific experiment at hand? If the goal is to establish a discrepancy with the null hypothesis and/or establish a pattern of order, because both requires ruling out equivalence, then NHST is a good tool ( Frick, 1996 ; Walker & Nowacki, 2011 ). If the goal is to test the presence of an effect and/or establish some quantitative values related to an effect, then NHST is not the method of choice since testing is conditioned on H0.

While a Bayesian analysis is suited to estimate that the probability that a hypothesis is correct, like NHST, it does not prove a theory on itself, but adds its plausibility ( Lindley, 2000 ). No matter what testing procedure is used and how strong results are, ( Fisher, 1959 p13) reminds us that ‘ […] no isolated experiment, however significant in itself, can suffice for the experimental demonstration of any natural phenomenon'. Similarly, the recent statement of the American Statistical Association ( Wasserstein & Lazar, 2016 ) makes it clear that conclusions should be based on the researchers understanding of the problem in context, along with all summary data and tests, and that no single value (being p-values, Bayesian factor or else) can be used support or invalidate a theory.

What to report and how?

Considering that quantitative reports will always have more information content than binary (significant or not) reports, we can always argue that raw and/or normalized effect size, confidence intervals, or Bayes factor must be reported. Reporting everything can however hinder the communication of the main result(s), and we should aim at giving only the information needed, at least in the core of a manuscript. Here I propose to adopt optimal reporting in the result section to keep the message clear, but have detailed supplementary material. When the hypothesis is about the presence/absence or order of an effect, and providing that a study has sufficient power, NHST is appropriate and it is sufficient to report in the text the actual p-value since it conveys the information needed to rule out equivalence. When the hypothesis and/or the discussion involve some quantitative value, and because p-values do not inform on the effect, it is essential to report on effect sizes ( Lakens, 2013 ), preferably accompanied with confidence or credible intervals. The reasoning is simply that one cannot predict and/or discuss quantities without accounting for variability. For the reader to understand and fully appreciate the results, nothing else is needed.

Because science progress is obtained by cumulating evidence ( Rosenthal, 1991 ), scientists should also consider the secondary use of the data. With today’s electronic articles, there are no reasons for not including all of derived data: mean, standard deviations, effect size, CI, Bayes factor should always be included as supplementary tables (or even better also share raw data). It is also essential to report the context in which tests were performed – that is to report all of the tests performed (all t, F, p values) because of the increase type one error rate due to selective reporting (multiple comparisons and p-hacking problems - Ioannidis, 2005 ). Providing all of this information allows (i) other researchers to directly and effectively compare their results in quantitative terms (replication of effects beyond significance, Open Science Collaboration, 2015 ), (ii) to compute power to future studies ( Lakens & Evers, 2014 ), and (iii) to aggregate results for meta-analyses whilst minimizing publication bias ( van Assen et al. , 2014 ).

[version 3; referees: 1 approved

Funding Statement

The author(s) declared that no grants were involved in supporting this work.

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Referee response for version 3

Dorothy vera margaret bishop.

1 Department of Experimental Psychology, University of Oxford, Oxford, UK

I can see from the history of this paper that the author has already been very responsive to reviewer comments, and that the process of revising has now been quite protracted.

That makes me reluctant to suggest much more, but I do see potential here for making the paper more impactful. So my overall view is that, once a few typos are fixed (see below), this could be published as is, but I think there is an issue with the potential readership and that further revision could overcome this.

I suspect my take on this is rather different from other reviewers, as I do not regard myself as a statistics expert, though I am on the more quantitative end of the continuum of psychologists and I try to keep up to date. I think I am quite close to the target readership , insofar as I am someone who was taught about statistics ages ago and uses stats a lot, but never got adequate training in the kinds of topic covered by this paper. The fact that I am aware of controversies around the interpretation of confidence intervals etc is simply because I follow some discussions of this on social media. I am therefore very interested to have a clear account of these issues.

This paper contains helpful information for someone in this position, but it is not always clear, and I felt the relevance of some of the content was uncertain. So here are some recommendations:

• As one previous reviewer noted, it’s questionable that there is a need for a tutorial introduction, and the limited length of this article does not lend itself to a full explanation. So it might be better to just focus on explaining as clearly as possible the problems people have had in interpreting key concepts. I think a title that made it clear this was the content would be more appealing than the current one.
• P 3, col 1, para 3, last sentence. Although statisticians always emphasise the arbitrary nature of p < .05, we all know that in practice authors who use other values are likely to have their analyses queried. I wondered whether it would be useful here to note that in some disciplines different cutoffs are traditional, e.g. particle physics. Or you could cite David Colquhoun’s paper in which he recommends using p < .001 ( http://rsos.royalsocietypublishing.org/content/1/3/140216) - just to be clear that the traditional p < .05 has been challenged.

What I can’t work out is how you would explain the alpha from Neyman-Pearson in the same way (though I can see from Figure 1 that with N-P you could test an alternative hypothesis, such as the idea that the coin would be heads 75% of the time).

‘By failing to reject, we simply continue to assume that H0 is true, which implies that one cannot….’ have ‘In failing to reject, we do not assume that H0 is true; one cannot argue against a theory from a non-significant result.’

I felt most readers would be interested to read about tests of equivalence and Bayesian approaches, but many would be unfamiliar with these and might like to see an example of how they work in practice – if space permitted.

• Confidence intervals: I simply could not understand the first sentence – I wondered what was meant by ‘builds’ here. I understand about difficulties in comparing CI across studies when sample sizes differ, but I did not find the last sentence on p 4 easy to understand.
• P 5: The sentence starting: ‘The alpha value has the same interpretation’ was also hard to understand, especially the term ‘1-alpha CI’. Here too I felt some concrete illustration might be helpful to the reader. And again, I also found the reference to Bayesian intervals tantalising – I think many readers won’t know how to compute these and something like a figure comparing a traditional CI with a Bayesian interval and giving a source for those who want to read on would be very helpful. The reference to ‘credible intervals’ in the penultimate paragraph is very unclear and needs a supporting reference – most readers will not be familiar with this concept.

P 3, col 1, para 2, line 2; “allows us to compute”

P 3, col 2, para 2, ‘probability of replicating’

P 3, col 2, para 2, line 4 ‘informative about’

P 3, col 2, para 4, line 2 delete ‘of’

P 3, col 2, para 5, line 9 – ‘conditioned’ is either wrong or too technical here: would ‘based’ be acceptable as alternative wording

P 3, col 2, para 5, line 13 ‘This dichotomisation allows one to distinguish’

P 3, col 2, para 5, last sentence, delete ‘Alternatively’.

P 3, col 2, last para line 2 ‘first’

P 4, col 2, para 2, last sentence is hard to understand; not sure if this is better: ‘If sample sizes differ between studies, the distribution of CIs cannot be specified a priori’

P 5, col 1, para 2, ‘a pattern of order’ – I did not understand what was meant by this

P 5, col 1, para 2, last sentence unclear: possible rewording: “If the goal is to test the size of an effect then NHST is not the method of choice, since testing can only reject the null hypothesis.’ (??)

P 5, col 1, para 3, line 1 delete ‘that’

P 5, col 1, para 3, line 3 ‘on’ -> ‘by’

P 5, col 2, para 1, line 4 , rather than ‘Here I propose to adopt’ I suggest ‘I recommend adopting’

P 5, col 2, para 1, line 13 ‘with’ -> ‘by’

P 5, col 2, para 1 – recommend deleting last sentence

P 5, col 2, para 2, line 2 ‘consider’ -> ‘anticipate’

P 5, col 2, para 2, delete ‘should always be included’

P 5, col 2, para 2, ‘type one’ -> ‘Type I’

I have read this submission. I believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard, however I have significant reservations, as outlined above.

The University of Edinburgh, UK

I wondered about changing the focus slightly and modifying the title to reflect this to say something like: Null hypothesis significance testing: a guide to commonly misunderstood concepts and recommendations for good practice

Thank you for the suggestion – you indeed saw the intention behind the ‘tutorial’ style of the paper.

• P 3, col 1, para 3, last sentence. Although statisticians always emphasise the arbitrary nature of p < .05, we all know that in practice authors who use other values are likely to have their analyses queried. I wondered whether it would be useful here to note that in some disciplines different cutoffs are traditional, e.g. particle physics. Or you could cite David Colquhoun’s paper in which he recommends using p < .001 ( http://rsos.royalsocietypublishing.org/content/1/3/140216)  - just to be clear that the traditional p < .05 has been challenged.

I have added a sentence on this citing Colquhoun 2014 and the new Benjamin 2017 on using .005.

I agree that this point is always hard to appreciate, especially because it seems like in practice it makes little difference. I added a paragraph but using reaction times rather than a coin toss – thanks for the suggestion.

Added an example based on new table 1, following figure 1 – giving CI, equivalence tests and Bayes Factor (with refs to easy to use tools)

Changed builds to constructs (this simply means they are something we build) and added that the implication that probability coverage is not warranty when sample size change, is that we cannot compare CI.

I changed ‘ i.e. we accept that 1-alpha CI are wrong in alpha percent of the times in the long run’ to ‘, ‘e.g. a 95% CI is wrong in 5% of the times in the long run (i.e. if we repeat the experiment many times).’ – for Bayesian intervals I simply re-cited Morey & Rouder, 2011.

It is not the CI cannot be specified, it’s that the interval is not predictive of anything anymore! I changed it to ‘If sample sizes, however, differ between studies, there is no warranty that a CI from one study will be true at the rate alpha in a different study, which implies that CI cannot be compared across studies at this is rarely the same sample sizes’

I added (i.e. establish that A > B) – we test that conditions are ordered, but without further specification of the probability of that effect nor its size

Yes it works – thx

P 5, col 2, para 2, ‘type one’ -> ‘Type I’ 

Typos fixed, and suggestions accepted – thanks for that.

Stephen J. Senn

1 Luxembourg Institute of Health, Strassen, L-1445, Luxembourg

The revisions are OK for me, and I have changed my status to Approved.

I have read this submission. I believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard.

Referee response for version 2

On the whole I think that this article is reasonable, my main reservation being that I have my doubts on whether the literature needs yet another tutorial on this subject.

A further reservation I have is that the author, following others, stresses what in my mind is a relatively unimportant distinction between the Fisherian and Neyman-Pearson (NP) approaches. The distinction stressed by many is that the NP approach leads to a dichotomy accept/reject based on probabilities established in advance, whereas the Fisherian approach uses tail area probabilities calculated from the observed statistic. I see this as being unimportant and not even true. Unless one considers that the person carrying out a hypothesis test (original tester) is mandated to come to a conclusion on behalf of all scientific posterity, then one must accept that any remote scientist can come to his or her conclusion depending on the personal type I error favoured. To operate the results of an NP test carried out by the original tester, the remote scientist then needs to know the p-value. The type I error rate is then compared to this to come to a personal accept or reject decision (1). In fact Lehmann (2), who was an important developer of and proponent of the NP system, describes exactly this approach as being good practice. (See Testing Statistical Hypotheses, 2nd edition P70). Thus using tail-area probabilities calculated from the observed statistics does not constitute an operational difference between the two systems.

A more important distinction between the Fisherian and NP systems is that the former does not use alternative hypotheses(3). Fisher's opinion was that the null hypothesis was more primitive than the test statistic but that the test statistic was more primitive than the alternative hypothesis. Thus, alternative hypotheses could not be used to justify choice of test statistic. Only experience could do that.

Further distinctions between the NP and Fisherian approach are to do with conditioning and whether a null hypothesis can ever be accepted.

I have one minor quibble about terminology. As far as I can see, the author uses the usual term 'null hypothesis' and the eccentric term 'nil hypothesis' interchangeably. It would be simpler if the latter were abandoned.

Referee response for version 1

Marcel alm van assen.

1 Department of Methodology and Statistics, Tilburgh University, Tilburg, Netherlands

Null hypothesis significance testing (NHST) is a difficult topic, with misunderstandings arising easily. Many texts, including basic statistics books, deal with the topic, and attempt to explain it to students and anyone else interested. I would refer to a good basic text book, for a detailed explanation of NHST, or to a specialized article when wishing an explaining the background of NHST. So, what is the added value of a new text on NHST? In any case, the added value should be described at the start of this text. Moreover, the topic is so delicate and difficult that errors, misinterpretations, and disagreements are easy. I attempted to show this by giving comments to many sentences in the text.

Abstract: “null hypothesis significance testing is the statistical method of choice in biological, biomedical and social sciences to investigate if an effect is likely”. No, NHST is the method to test the hypothesis of no effect.

Intro: “Null hypothesis significance testing (NHST) is a method of statistical inference by which an observation is tested against a hypothesis of no effect or no relationship.” What is an ‘observation’? NHST is difficult to describe in one sentence, particularly here. I would skip this sentence entirely, here.

Section on Fisher; also explain the one-tailed test.

Section on Fisher; p(Obs|H0) does not reflect the verbal definition (the ‘or more extreme’ part).

Section on Fisher; use a reference and citation to Fisher’s interpretation of the p-value

Section on Fisher; “This was however only intended to be used as an indication that there is something in the data that deserves further investigation. The reason for this is that only H0 is tested whilst the effect under study is not itself being investigated.” First sentence, can you give a reference? Many people say a lot about Fisher’s intentions, but the good man is dead and cannot reply… Second sentence is a bit awkward, because the effect is investigated in a way, by testing the H0.

Section on p-value; Layout and structure can be improved greatly, by first again stating what the p-value is, and then statement by statement, what it is not, using separate lines for each statement. Consider adding that the p-value is randomly distributed under H0 (if all the assumptions of the test are met), and that under H1 the p-value is a function of population effect size and N; the larger each is, the smaller the p-value generally is.

Skip the sentence “If there is no effect, we should replicate the absence of effect with a probability equal to 1-p”. Not insightful, and you did not discuss the concept ‘replicate’ (and do not need to).

Skip the sentence “The total probability of false positives can also be obtained by aggregating results ( Ioannidis, 2005 ).” Not strongly related to p-values, and introduces unnecessary concepts ‘false positives’ (perhaps later useful) and ‘aggregation’.

Consider deleting; “If there is an effect however, the probability to replicate is a function of the (unknown) population effect size with no good way to know this from a single experiment ( Killeen, 2005 ).”

The following sentence; “ Finally, a (small) p-value  is not an indication favouring a hypothesis . A low p-value indicates a misfit of the null hypothesis to the data and cannot be taken as evidence in favour of a specific alternative hypothesis more than any other possible alternatives such as measurement error and selection bias ( Gelman, 2013 ).” is surely not mainstream thinking about NHST; I would surely delete that sentence. In NHST, a p-value is used for testing the H0. Why did you not yet discuss significance level? Yes, before discussing what is not a p-value, I would explain NHST (i.e., what it is and how it is used). 

Also the next sentence “The more (a priori) implausible the alternative hypothesis, the greater the chance that a finding is a false alarm ( Krzywinski & Altman, 2013 ;  Nuzzo, 2014 ).“ is not fully clear to me. This is a Bayesian statement. In NHST, no likelihoods are attributed to hypotheses; the reasoning is “IF H0 is true, then…”.

Last sentence: “As  Nickerson (2000)  puts it ‘theory corroboration requires the testing of multiple predictions because the chance of getting statistically significant results for the wrong reasons in any given case is high’.” What is relation of this sentence to the contents of this section, precisely?

Next section: “For instance, we can estimate that the probability of a given F value to be in the critical interval [+2 +∞] is less than 5%” This depends on the degrees of freedom.

“When there is no effect (H0 is true), the erroneous rejection of H0 is known as type I error and is equal to the p-value.” Strange sentence. The Type I error is the probability of erroneously rejecting the H0 (so, when it is true). The p-value is … well, you explained it before; it surely does not equal the Type I error.

Consider adding a figure explaining the distinction between Fisher’s logic and that of Neyman and Pearson.

“When the test statistics falls outside the critical region(s)” What is outside?

“There is a profound difference between accepting the null hypothesis and simply failing to reject it ( Killeen, 2005 )” I agree with you, but perhaps you may add that some statisticians simply define “accept H0’” as obtaining a p-value larger than the significance level. Did you already discuss the significance level, and it’s mostly used values?

“To accept or reject equally the null hypothesis, Bayesian approaches ( Dienes, 2014 ;  Kruschke, 2011 ) or confidence intervals must be used.” Is ‘reject equally’ appropriate English? Also using Cis, one cannot accept the H0.

Do you start discussing alpha only in the context of Cis?

“CI also indicates the precision of the estimate of effect size, but unless using a percentile bootstrap approach, they require assumptions about distributions which can lead to serious biases in particular regarding the symmetry and width of the intervals ( Wilcox, 2012 ).” Too difficult, using new concepts. Consider deleting.

“Assuming the CI (a)symmetry and width are correct, this gives some indication about the likelihood that a similar value can be observed in future studies, with 95% CI giving about 83% chance of replication success ( Lakens & Evers, 2014 ).” This statement is, in general, completely false. It very much depends on the sample sizes of both studies. If the replication study has a much, much, much larger N, then the probability that the original CI will contain the effect size of the replication approaches (1-alpha)*100%. If the original study has a much, much, much larger N, then the probability that the original Ci will contain the effect size of the replication study approaches 0%.

“Finally, contrary to p-values, CI can be used to accept H0. Typically, if a CI includes 0, we cannot reject H0. If a critical null region is specified rather than a single point estimate, for instance [-2 +2] and the CI is included within the critical null region, then H0 can be accepted. Importantly, the critical region must be specified a priori and cannot be determined from the data themselves.” No. H0 cannot be accepted with Cis.

“The (posterior) probability of an effect can however not be obtained using a frequentist framework.” Frequentist framework? You did not discuss that, yet.

“X% of times the CI obtained will contain the same parameter value”. The same? True, you mean?

“e.g. X% of the times the CI contains the same mean” I do not understand; which mean?

“The alpha value has the same interpretation as when using H0, i.e. we accept that 1-alpha CI are wrong in alpha percent of the times. “ What do you mean, CI are wrong? Consider rephrasing.

“To make a statement about the probability of a parameter of interest, likelihood intervals (maximum likelihood) and credibility intervals (Bayes) are better suited.” ML gives the likelihood of the data given the parameter, not the other way around.

“Many of the disagreements are not on the method itself but on its use.” Bayesians may disagree.

“If the goal is to establish the likelihood of an effect and/or establish a pattern of order, because both requires ruling out equivalence, then NHST is a good tool ( Frick, 1996 )” NHST does not provide evidence on the likelihood of an effect.

“If the goal is to establish some quantitative values, then NHST is not the method of choice.” P-values are also quantitative… this is not a precise sentence. And NHST may be used in combination with effect size estimation (this is even recommended by, e.g., the American Psychological Association (APA)).

“Because results are conditioned on H0, NHST cannot be used to establish beliefs.” It can reinforce some beliefs, e.g., if H0 or any other hypothesis, is true.

“To estimate the probability of a hypothesis, a Bayesian analysis is a better alternative.” It is the only alternative?

“Note however that even when a specific quantitative prediction from a hypothesis is shown to be true (typically testing H1 using Bayes), it does not prove the hypothesis itself, it only adds to its plausibility.” How can we show something is true?

I do not agree on the contents of the last section on ‘minimal reporting’. I prefer ‘optimal reporting’ instead, i.e., the reporting the information that is essential to the interpretation of the result, to any ready, which may have other goals than the writer of the article. This reporting includes, for sure, an estimate of effect size, and preferably a confidence interval, which is in line with recommendations of the APA.

I have read this submission. I believe that I have an appropriate level of expertise to state that I do not consider it to be of an acceptable scientific standard, for reasons outlined above.

The idea of this short review was to point to common interpretation errors (stressing again and again that we are under H0) being in using p-values or CI, and also proposing reporting practices to avoid bias. This is now stated at the end of abstract.

Regarding text books, it is clear that many fail to clearly distinguish Fisher/Pearson/NHST, see Glinet et al (2012) J. Exp Education 71, 83-92. If you have 1 or 2 in mind that you know to be good, I’m happy to include them.

I agree – yet people use it to investigate (not test) if an effect is likely. The issue here is wording. What about adding this distinction at the end of the sentence?: ‘null hypothesis significance testing is the statistical method of choice in biological, biomedical and social sciences used to investigate if an effect is likely, even though it actually tests for the hypothesis of no effect’.

I think a definition is needed, as it offers a starting point. What about the following: ‘NHST is a method of statistical inference by which an experimental factor is tested against a hypothesis of no effect or no relationship based on a given observation’

The section on Fisher has been modified (more or less) as suggested: (1) avoiding talking about one or two tailed tests (2) updating for p(Obs≥t|H0) and (3) referring to Fisher more explicitly (ie pages from articles and book) ; I cannot tell his intentions but these quotes leave little space to alternative interpretations.

The reasoning here is as you state yourself, part 1: ‘a p-value is used for testing the H0; and part 2: ‘no likelihoods are attributed to hypotheses’ it follows we cannot favour a hypothesis. It might seems contentious but this is the case that all we can is to reject the null – how could we favour a specific alternative hypothesis from there? This is explored further down the manuscript (and I now point to that) – note that we do not need to be Bayesian to favour a specific H1, all I’m saying is this cannot be attained with a p-value.

The point was to emphasise that a p value is not there to tell us a given H1 is true and can only be achieved through multiple predictions and experiments. I deleted it for clarity.

This sentence has been removed

Indeed, you are right and I have modified the text accordingly. When there is no effect (H0 is true), the erroneous rejection of H0 is known as type 1 error. Importantly, the type 1 error rate, or alpha value is determined a priori. It is a common mistake but the level of significance (for a given sample) is not the same as the frequency of acceptance alpha found on repeated sampling (Fisher, 1955).

A figure is now presented – with levels of acceptance, critical region, level of significance and p-value.

I should have clarified further here – as I was having in mind tests of equivalence. To clarify, I simply states now: ‘To accept the null hypothesis, tests of equivalence or Bayesian approaches must be used.’

It is now presented in the paragraph before.

Yes, you are right, I completely overlooked this problem. The corrected sentence (with more accurate ref) is now “Assuming the CI (a)symmetry and width are correct, this gives some indication about the likelihood that a similar value can be observed in future studies. For future studies of the same sample size, 95% CI giving about 83% chance of replication success (Cumming and Mallardet, 2006). If sample sizes differ between studies, CI do not however warranty any a priori coverage”.

Again, I had in mind equivalence testing, but in both cases you are right we can only reject and I therefore removed that sentence.

Yes, p-values must be interpreted in context with effect size, but this is not what people do. The point here is to be pragmatic, does and don’t. The sentence was changed.

Not for testing, but for probability, I am not aware of anything else.

Cumulative evidence is, in my opinion, the only way to show it. Even in hard science like physics multiple experiments. In the recent CERN study on finding Higgs bosons, 2 different and complementary experiments ran in parallel – and the cumulative evidence was taken as a proof of the true existence of Higgs bosons.

Daniel Lakens

1 School of Innovation Sciences, Eindhoven University of Technology, Eindhoven, Netherlands

I appreciate the author's attempt to write a short tutorial on NHST. Many people don't know how to use it, so attempts to educate people are always worthwhile. However, I don't think the current article reaches it's aim. For one, I think it might be practically impossible to explain a lot in such an ultra short paper - every section would require more than 2 pages to explain, and there are many sections. Furthermore, there are some excellent overviews, which, although more extensive, are also much clearer (e.g., Nickerson, 2000 ). Finally, I found many statements to be unclear, and perhaps even incorrect (noted below). Because there is nothing worse than creating more confusion on such a topic, I have extremely high standards before I think such a short primer should be indexed. I note some examples of unclear or incorrect statements below. I'm sorry I can't make a more positive recommendation.

“investigate if an effect is likely” – ambiguous statement. I think you mean, whether the observed DATA is probable, assuming there is no effect?

The Fisher (1959) reference is not correct – Fischer developed his method much earlier.

“This p-value thus reflects the conditional probability of achieving the observed outcome or larger, p(Obs|H0)” – please add 'assuming the null-hypothesis is true'.

“p(Obs|H0)” – explain this notation for novices.

“Following Fisher, the smaller the p-value, the greater the likelihood that the null hypothesis is false.”  This is wrong, and any statement about this needs to be much more precise. I would suggest direct quotes.

“there is something in the data that deserves further investigation” –unclear sentence.

“The reason for this” – unclear what ‘this’ refers to.

“ not the probability of the null hypothesis of being true, p(H0)” – second of can be removed?

“Any interpretation of the p-value in relation to the effect under study (strength, reliability, probability) is indeed

wrong, since the p-value is conditioned on H0”  - incorrect. A big problem is that it depends on the sample size, and that the probability of a theory depends on the prior.

“If there is no effect, we should replicate the absence of effect with a probability equal to 1-p.” I don’t understand this, but I think it is incorrect.

“The total probability of false positives can also be obtained by aggregating results (Ioannidis, 2005).” Unclear, and probably incorrect.

“By failing to reject, we simply continue to assume that H0 is true, which implies that one cannot, from a nonsignificant result, argue against a theory” – according to which theory? From a NP perspective, you can ACT as if the theory is false.

“(Lakens & Evers, 2014”) – we are not the original source, which should be cited instead.

“ Typically, if a CI includes 0, we cannot reject H0.”  - when would this not be the case? This assumes a CI of 1-alpha.

“If a critical null region is specified rather than a single point estimate, for instance [-2 +2] and the CI is included within the critical null region, then H0 can be accepted.” – you mean practically, or formally? I’m pretty sure only the former.

The section on ‘The (correct) use of NHST’ seems to conclude only Bayesian statistics should be used. I don’t really agree.

“ we can always argue that effect size, power, etc. must be reported.” – which power? Post-hoc power? Surely not? Other types are unknown. So what do you mean?

The recommendation on what to report remains vague, and it is unclear why what should be reported.

This sentence was changed, following as well the other reviewer, to ‘null hypothesis significance testing is the statistical method of choice in biological, biomedical and social sciences to investigate if an effect is likely, even though it actually tests whether the observed data are probable, assuming there is no effect’

Changed, refers to Fisher 1925

I changed a little the sentence structure, which should make explicit that this is the condition probability.

This has been changed to ‘[…] to decide whether the evidence is worth additional investigation and/or replication (Fisher, 1971 p13)’

my mistake – the sentence structure is now ‘ not the probability of the null hypothesis p(H0), of being true,’ ; hope this makes more sense (and this way refers back to p(Obs>t|H0)

Fair enough – my point was to stress the fact that p value and effect size or H1 have very little in common, but yes that the part in common has to do with sample size. I left the conditioning on H0 but also point out the dependency on sample size.

The whole paragraph was changed to reflect a more philosophical take on scientific induction/reasoning. I hope this is clearer.

Changed to refer to equivalence testing

I rewrote this, as to show frequentist analysis can be used  - I’m trying to sell Bayes more than any other approach.

I’m arguing we should report it all, that’s why there is no exhausting list – I can if needed.

Chapter 7 Hypothesis Testing

Aug 14, 2012

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7-1 Basics of Hypothesis Testing 7-2 Testing a Claim about a Mean: Large Samples 7-3 Testing a Claim about a Mean: Small Samples 7-4 Testing a Claim about a Proportion 7- 5 Testing a Claim about a Standard     Deviation (will cover with chap 8). Chapter 7 Hypothesis Testing. 7-1.

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7-1 Basics of Hypothesis Testing 7-2 Testing a Claim about a Mean: Large Samples 7-3 Testing a Claim about a Mean: Small Samples 7-4 Testing a Claim about a Proportion 7- 5 Testing a Claim about a Standard     Deviation (will cover with chap 8) Chapter 7Hypothesis Testing

7-1 Basics of Hypothesis Testing

Hypothesis in statistics, is a statement regarding a characteristic of one or more populations Definition

Statement is made about the population Evidence in collected to test the statement Data is analyzed to assess the plausibility of the statement Steps in Hypothesis Testing

Components of aFormal Hypothesis Test

Form Hypothesis Calculate Test Statistic Choose Significance Level Find Critical Value(s) Conclusion Components of a Hypothesis Test

A hypothesis set up to be nullified or refuted in order to support an alternate hypothesis. When used, the null hypothesis is presumed true until statistical evidence in the form of a hypothesis test indicates otherwise. Null Hypothesis: H0

Statement about value of population parameter like m, p or s Must contain condition of equality =, , or Test the Null Hypothesis directly RejectH0 or fail to rejectH0 Null Hypothesis: H0

Must be true if H0 is false , <, > ‘opposite’ of Null sometimes used instead of Alternative Hypothesis: H1 H1 Ha

If you are conducting a study and want to use a hypothesis test to support your claim, the claim must be worded so that it becomes the alternative hypothesis. The null hypothesis must contain the condition of equality Note about Forming Your Own Claims (Hypotheses)

Set up the null and alternative hypothesis The packaging on a lightbulb states that the bulb will last 500 hours. A consumer advocate would like to know if the mean lifetime of a bulb is different than 500 hours. A drug to lower blood pressure advertises that it drops blood pressure by 20%. A doctor that prescribes this medication believes that it is less. Set up the null and alternative hypothesis. (see hw # 1) Examples

a value computed from the sample data that is used in making the decision about the rejection of the null hypothesis Testing claims about the population proportion Test Statistic x - µ σ Z*= n

Critical Region - Set of all values of the test statistic that would cause a rejection of the null hypothesis Critical Value - Value or values that separate the critical region from the values of the test statistics that do not lead to a rejection of the null hypothesis

One Tailed Test Critical Region and Critical Value Critical Region Critical Value ( z score )

Two Tailed Test Critical Region and Critical Value Critical Regions Critical Value ( z score ) Critical Value ( z score )

Denoted by  The probability that the test statistic will fall in the critical region when the null hypothesis is actually true. Common choices are 0.05, 0.01, and 0.10 Significance Level

Two-tailed,Right-tailed,Left-tailed Tests The tails in a distribution are the extreme regions bounded by critical values.

H0: µ = 100 H1: µ  100 Two-tailed Test  is divided equally between the two tails of the critical region Means less than or greater than Reject H0 Fail to reject H0 Reject H0 100 Values that differ significantly from 100

H0: µ  100 H1: µ > 100 Fail to reject H0 Reject H0 Right-tailed Test Points Right Values that differ significantly from 100 100

H0: µ  100 H1: µ < 100 Left-tailed Test Points Left Reject H0 Fail to reject H0 Values that differ significantly from 100 100

Traditional Method Reject H0if the test statistic falls in the critical region Fail to reject H0if the test statistic does not fall in the critical region P-Value Method Reject H0if the P-value is less than or equal  Fail to reject H0if the P-value is greater than the  Conclusions in Hypothesis Testing

Finds the probability (P-value) of getting a result and rejects the null hypothesis if that probability is very low Uses test statistic to find the probability. Method used by most computer programs and calculators. Will prefer that you use the traditional method on HW and Tests P-Value Methodof Testing Hypotheses

Two tailed test p(z>a) + p(z<-a) One tailed test (right) p(z>a) One tailed test (left) p(z<-a) Finding P-values Where “a” is the value of the calculated test statistic Used for HW # 3 – 5 – see example on next two slides

Determine P-value Sample data: x = 105 or z* = 2.66 Reject H0: µ = 100 Fail to Reject H0: µ = 100 * µ = 73.4 or z = 0 z = 1.96 z* = 2.66 Just find p(z > 2.66)

Determine P-value Sample data: x = 105 or z* = 2.66 Reject H0: µ = 100 Reject H0: µ = 100 Fail to Reject H0: µ = 100 * z = - 1.96 µ = 73.4 or z = 0 z = 1.96 z* = 2.66 Just find p(z > 2.66) + p(z < -2.66)

Always test the null hypothesis Choose one of two possible conclusions 1. Reject the H0 2. Fail to reject the H0 Conclusions in Hypothesis Testing

Never “accept the null hypothesis, we will fail to reject it. Will discuss this in more detail in a moment We are not proving the null hypothesis Sample evidence is not strong enough to warrant rejection (such as not enough evidence to convict a suspect – guilty vs. not guilty) Accept versus Fail to Reject

Accept versus Fail to Reject

Need to formulate correct wording of finalconclusion Conclusions in Hypothesis Testing

Wording of final conclusion 1. Reject the H0 Conclusion: There is sufficient evidence to conclude………………………(what ever H1 says) 2. Fail to reject the H0 Conclusion: There is not sufficient evidence to conclude ……………………(what ever H1 says) Conclusions in Hypothesis Testing

State a conclusion The proportion of college graduates how smoke is less than 27%. Reject Ho: The mean weights of men at FLC is different from 180 lbs. Fail to Reject Ho: Example Used for #6 on HW

The mistake of rejecting the null hypothesis when it is true. (alpha) is used to represent the probability of a type I error Example: Rejecting a claim that the mean body temperature is 98.6 degrees when the mean really does equal 98.6 (test question) Type I Error

the mistake of failing to reject the null hypothesis when it is false. ß (beta) is used to represent the probability of a type II error Example: Failing to reject the claim that the mean body temperature is 98.6 degrees when the mean is really different from 98.6 (test question) Type II Error

Type I and Type II Errors True State of Nature H0 True H0 False Reject H0 Correct decision Type I error  Decision Fail to Reject H0 Type II error  Correct decision In this class we will focus on controlling a Type I error. However, you will have one question on the exam asking you to differentiate between the two.

a = p(rejecting a true null hypothesis) b = p(failing to reject a false null hypothesis) n, a and b are all related Type I and Type II Errors

Identify the type I and type II error. The mean IQ of statistics teachers is greater than 120. Type I: We reject the mean IQ of statistics teachers is 120 when it really is 120. Type II: We fail to reject the mean IQ of statistics teachers is 120 when it really isn’t 120. Example

For any fixed sample size n, as  decreases,  increases and conversely. To decrease both  and , increase the sample size. Controlling Type I and Type II Errors

Power of a Hypothesis Test is the probability (1 - ) of rejecting a false null hypothesis. Note: No exam questions on this. Usually covered in a more advanced class in statistics. Definition

7-2 Testing a claim about the mean (large samples)

Goal Identify a sample result that is significantly different from the claimed value By Comparing the test statistic to the critical value Traditional (or Classical) Method of Testing Hypotheses

Determine H0 and H1. (and if necessary) Determine the correct test statistic and calculate. Determine the critical values, the critical region and sketch a graph. Determine Reject H0 or Fail to reject H0 State your conclusion in simple non technical terms. Traditional (or Classical) Method of Testing Hypotheses (MAKE SURE THIS IS IN YOUR NOTES)

Test Statistic for Testing a Claim about a Proportion Can Use Traditional method Or P-value method

1) Traditional method 2) P-value method 3) Confidence intervals Three Methods Discussed

for testing claims about population means 1) The sample is a random sample. 2) The sample is large (n > 30). a) Central limit theorem applies b) Can use normal distribution 3) If  is unknown, we can use sample standard deviation s as estimate for . Assumptions

Test Statistic for Claims about µ when n > 30 x - µx Z*=  n

Reject the null hypothesis if the test statistic is in the critical region Fail to reject the null hypothesis if the test statistic is not in the critical region Decision Criterion

Claim:  = 69.5 years H0 :  = 69.5 H1 :  69.5 Example:A newspaper article noted that the mean life span for 35 male symphony conductors was 73.4 years, in contrast to the mean of 69.5 years for males in the general population. Test the claim that there is a difference. Assume a standard deviation of 8.7 years. Choose your own significance level. Step 1: Set up Claim, H0, H1 Select if necessary level:  = 0.05

Step 2: Identify the test statistic and calculate x - µ 73.4 – 69.5 z*=== 2.65  8.7 n 35

Step 3: Determine critical region(s) and critical value(s) & Sketch = 0.05 /2= 0.025 (two tailed test) 0.4750 0.4750 0.025 0.025 z = - 1.96 1.96 Critical Values - Calculator

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Chapter 8 Hypothesis Testing

Chapter 8 Hypothesis Testing. 8.2 Basics of Hypothesis Testing 8.3 Testing about a Proportion p 8.4 Testing about a Mean µ ( σ known ) 8.5 Testing about a Mean µ ( σ unknown ) 8.6 Testing about a Standard Deviation σ. Section 8.2 Basics of Hypothesis Testing. Objective

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Chapter 9 Hypothesis Testing

Chapter 9 Hypothesis Testing. 9.1 The Language of Hypothesis Testing. Example: Illustrating Hypothesis Testing.

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Chapter 10: Hypothesis Testing. Outline (Topics from 10.2 and 10.4). Hypothesis Testing Definitions The p value Examples and summary of steps Significance levels. Z-test for means and proportions. Tests of significance. How do we determine how good our estimate of s parameter is?

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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, 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.

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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