Category Archives: Post-Hoc Power

Meta-Analysis of Observed Power: Comparison of Estimation Methods

April 1, 2015Median Observed Power, Meta-Analysis, Observed Power, Pcurve, Post-Hoc Power, Posteriori Power Analysis, Publication Bias, Puniform, Questionable Research Practices, r-index, YMCA, Yuan-Maxwell, Yuan-Maxwell Correction, Yuan-Maxwell-Corrected-AverageMeta-Analysis, Meta-Science, replicability, Replication, ScienceUlrich Schimmack

Meta-Analysis of Observed Power

Citation: Dr. R (2015). Meta-analysis of observed power. R-Index Bulletin, Vol(1), A2.

In a previous blog post, I presented an introduction to the concept of observed power. Observed power is an estimate of the true power on the basis of observed effect size, sampling error, and significance criterion of a study. Yuan and Maxwell (2005) concluded that observed power is a useless construct when it is applied to a single study, mainly because sampling error in a single study is too large to obtain useful estimates of true power. However, sampling error decreases as the number of studies increases and observed power in a set of studies can provide useful information about the true power in a set of studies.

This blog post introduces various methods that can be used to estimate power on the basis of a set of studies (meta-analysis). I then present simulation studies that compare the various estimation methods in terms of their ability to estimate true power under a variety of conditions. In this blog post, I examine only unbiased sets of studies. That is, the sample of studies in a meta-analysis is a representative sample from the population of studies with specific characteristics. The first simulation assumes that samples are drawn from a population of studies with fixed effect size and fixed sampling error. As a result, all studies have the same true power (homogeneous). The second simulation assumes that all studies have a fixed effect size, but that sampling error varies across studies. As power is a function of effect size and sampling error, this simulation models heterogeneity in true power. The next simulations assume heterogeneity in population effect sizes. One simulation uses a normal distribution of effect sizes. Importantly, a normal distribution has no influence on the mean because effect sizes are symmetrically distributed around the mean effect size. The next simulations use skewed normal distributions. This simulation provides a realistic scenario for meta-analysis of heterogeneous sets of studies such as a meta-analysis of articles in a specific journal or articles on different topics published by the same author.

Observed Power Estimation Method 1: The Percentage of Significant Results

The simplest method to determine observed power is to compute the percentage of significant results. As power is defined as the long-range percentage of significant results, the percentage of significant results in a set of studies is an unbiased estimate of the long-term percentage. The main limitation of this method is that the dichotomous measure (significant versus insignificant) is likely to be imprecise when the number of studies is small. For example, two studies can only show observed power values of 0, 25%, 50%, or 100%, even if true power were 75%. However, the percentage of significant results plays an important role in bias tests that examine whether a set of studies is representative. When researchers hide non-significant results or use questionable research methods to produce significant results, the percentage of significant results will be higher than the percentage of significant results that could have been obtained on the basis of the actual power to produce significant results.

Observed Power Estimation Method 2: The Median

Schimmack (2012) proposed to average observed power of individual studies to estimate observed power. Yuan and Maxwell (2005) demonstrated that the average of observed power is a biased estimator of true power. It overestimates power when power is less than 50% and it underestimates true power when power is above 50%. Although the bias is not large (no more than 10 percentage points), Yuan and Maxwell (2005) proposed a method that produces an unbiased estimate of power in a meta-analysis of studies with the same true power (exact replication studies). Unlike the average that is sensitive to skewed distributions, the median provides an unbiased estimate of true power because sampling error is equally likely (50:50 probability) to inflate or deflate the observed power estimate. To avoid the bias of averaging observed power, Schimmack (2014) used median observed power to estimate the replicability of a set of studies.

Observed Power Estimation Method 3: P-Curve’s KS Test

Another method is implemented in Simonsohn’s (2014) pcurve. Pcurve was developed to obtain an unbiased estimate of a population effect size from a biased sample of studies. To achieve this goal, it is necessary to determine the power of studies because bias is a function of power. The pcurve estimation uses an iterative approach that tries out different values of true power. For each potential value of true power, it computes the location (quantile) of observed test statistics relative to a potential non-centrality parameter. The best fitting non-centrality parameter is located in the middle of the observed test statistics. Once a non-central distribution has been found, it is possible to assign each observed test-value a cumulative percentile of the non-central distribution. For the actual non-centrality parameter, these percentiles have a uniform distribution. To find the best fitting non-centrality parameter from a set of possible parameters, pcurve tests whether the distribution of observed percentiles follows a uniform distribution using the Kolmogorov-Smirnov test. The non-centrality parameter with the smallest test statistics is then used to estimate true power.

Observed Power Estimation Method 4: P-Uniform

van Assen, van Aert, and Wicherts (2014) developed another method to estimate observed power. Their method is based on the use of the gamma distribution. Like the pcurve method, this method relies on the fact that observed test-statistics should follow a uniform distribution when a potential non-centrality parameter matches the true non-centrality parameter. P-uniform transforms the probabilities given a potential non-centrality parameter with a negative log-function (-log[x]). These values are summed. When probabilities form a uniform distribution, the sum of the log-transformed probabilities matches the number of studies. Thus, the value with the smallest absolute discrepancy between the sum of negative log-transformed percentages and the number of studies provides the estimate of observed power.

Observed Power Estimation Method 5: Averaging Standard Normal Non-Centrality Parameter

In addition to these existing methods, I introduce to novel estimation methods. The first new method converts observed test statistics into one-sided p-values. These p-values are then transformed into z-scores. This approach has a long tradition in meta-analysis that was developed by Stouffer et al. (1949). It was popularized by Rosenthal during the early days of meta-analysis (Rosenthal, 1979). Transformation of probabilities into z-scores makes it easy to aggregate probabilities because z-scores follow a symmetrical distribution. The average of these z-scores can be used as an estimate of the actual non-centrality parameter. The average z-score can then be used to estimate true power. This approach avoids the problem of averaging power estimates that power has a skewed distribution. Thus, it should provide an unbiased estimate of true power when power is homogenous across studies.

Observed Power Estimation Method 6: Yuan-Maxwell Correction of Average Observed Power

Yuan and Maxwell (2005) demonstrated a simple average of observed power is systematically biased. However, a simple average avoids the problems of transforming the data and can produce tighter estimates than the median method. Therefore I explored whether it is possible to apply a correction to the simple average. The correction is based on Yuan and Maxwell’s (2005) mathematically derived formula for systematic bias. After averaging observed power, Yuan and Maxwell’s formula for bias is used to correct the estimate for systematic bias. The only problem with this approach is that bias is a function of true power. However, as observed power becomes an increasingly good estimator of true power in the long run, the bias correction will also become increasingly better at correcting the right amount of bias.

The Yuan-Maxwell correction approach is particularly promising for meta-analysis of heterogeneous sets of studies such as sets of diverse studies in a journal. The main advantage of this method is that averaging of power makes no assumptions about the distribution of power across different studies (Schimmack, 2012). The main limitation of averaging power was the systematic bias, but Yuan and Maxwell’s formula makes it possible to reduce this systematic bias, while maintaining the advantage of having a method that can be applied to heterogeneous sets of studies.

RESULTS

Homogeneous Effect Sizes and Sample Sizes

The first simulation used 100 effect sizes ranging from .01 to 1.00 and 50 sample sizes ranging from 11 to 60 participants per condition (Ns = 22 to 120), yielding 5000 different populations of studies. The true power of these studies was determined on the basis of the effect size, sample size, and the criterion p < .025 (one-tailed), which is equivalent to .05 (two-tailed). Sample sizes were chosen so that average power across the 5,000 studies was 50%. The simulation drew 10 random samples from each of the 5,000 populations of studies. Each sample of a study simulated a between-subject design with the given population effect size and sample size. The results were stored as one-tailed p-values. For the meta-analysis p-values were converted into z-scores. To avoid biases due to extreme outliers, z-scores greater than 5 were set to 5 (observed power = .999).

The six estimation methods were then used to compute observed power on the basis of samples of 10 studies. The following figures show observed power as a function of true power. The green lines show the 95% confidence interval for different levels of true power. The figure also includes red dashed lines for a value of 50% power. Studies with more than 50% observed power would be significant. Studies with less than 50% observed power would be non-significant. The figures also include a blue line for 80% true power. Cohen (1988) recommended that researchers should aim for a minimum of 80% power. It is instructive how accurate estimation methods are in evaluating whether a set of studies met this criterion.

The histogram shows the distribution of true power across the 5,000 populations of studies.

The histogram shows that the simulation covers the full range of power. It also shows that high-powered studies are overrepresented because moderate to large effect sizes can achieve high power for a wide range of sample sizes. The distribution is not important for the evaluation of different estimation methods and benefits all estimation methods equally because observed power is a good estimator of true power when true power is close to the maximum (Yuan & Maxwell, 2005).

The next figure shows scatterplots of observed power as a function of true power. Values above the diagonal indicate that observed power overestimates true power. Values below the diagonal show that observed power underestimates true power.

Visual inspection of the plots suggests that all methods provide unbiased estimates of true power. Another observation is that the count of significant results provides the least accurate estimates of true power. The reason is simply that aggregation of dichotomous variables requires a large number of observations to approximate true power. The third observation is that visual inspection provides little information about the relative accuracy of the other methods. Finally, the plots show how accurate observed power estimates are in meta-analysis of 10 studies. When true power is 50%, estimates very rarely exceed 80%. Similarly, when true power is above 80%, observed power is never below 50%. Thus, observed power can be used to examine whether a set of studies met Cohen’s recommended guidelines to conduct studies with a minimum of 80% power. If observed power is 50%, it is nearly certain that the studies did not have the recommended 80% power.

To examine the relative accuracy of different estimation methods quantitatively, I computed bias scores (observed power – true power). As bias can overestimate and underestimate true power, the standard deviation of these bias scores can be used to quantify the precision of various estimation methods. In addition, I present the mean to examine whether a method has large sample accuracy (i.e. the bias approaches zero as the number of simulations increases). I also present the percentage of studies with no more than 20% points bias. Although 20% bias may seem large, it is not important to estimate power with very high precision. When observed power is below 50%, it suggests that a set of studies was underpowered even if the observed power estimate is an underestimation.

The quantitative analysis also shows no meaningful differences among the estimation methods. The more interesting question is how these methods perform under more challenging conditions when the set of studies are no longer exact replication studies with fixed power.

Homogeneous Effect Size, Heterogeneous Sample Sizes

The next simulation simulated variation in sample sizes. For each population of studies, sample sizes were varied by multiplying a particular sample size by factors of 1 to 5.5 (1.0, 1.5,2.0…,5.5). Thus, a base-sample-size of 40 created a range of sample sizes from 40 to 220. A base-sample size of 100 created a range of sample sizes from 100 to 2,200. As variation in sample sizes increases the average sample size, the range of effect sizes was limited to a range from .004 to .4 and effect sizes were increased in steps of d = .004. The histogram shows the distribution of power in the 5,000 population of studies.

The simulation covers the full range of true power, although studies with low and very high power are overrepresented.

The results are visually not distinguishable from those in the previous simulation.

The quantitative comparison of the estimation methods also shows very similar results.

In sum, all methods perform well even when true power varies as a function of variation in sample sizes. This conclusion may not generalize to more extreme simulations of variation in sample sizes, but more extreme variations in sample sizes would further increase the average power of a set of studies because the average sample size would increase as well. Thus, variation in effect sizes poses a more realistic challenge for the different estimation methods.

Heterogeneous, Normally Distributed Effect Sizes

The next simulation used a random normal distribution of true effect sizes. Effect sizes were simulated to have a reasonable but large variation. Starting effect sizes ranged from .208 to 1.000 and increased in increments of .008. Sample sizes ranged from 10 to 60 and increased in increments of 2 to create 5,000 populations of studies. For each population of studies, effect sizes were sampled randomly from a normal distribution with a standard deviation of SD = .2. Extreme effect sizes below d = -.05 were set to -.05 and extreme effect sizes above d = 1.20 were set to 1.20. The first histogram of effect sizes shows the 50,000 population effect sizes. The histogram on the right shows the distribution of true power for the 5,000 sets of 10 studies.

The plots of observed and true power show that the estimation methods continue to perform rather well even when population effect sizes are heterogeneous and normally distributed.

The quantitative comparison suggests that puniform has some problems with heterogeneity. More detailed studies are needed to examine whether this is a persistent problem for puniform, but given the good performance of the other methods it seems easier to use these methods.

Heterogeneous, Skewed Normal Effect Sizes

The next simulation puts the estimation methods to a stronger challenge by introducing skewed distributions of population effect sizes. For example, a set of studies may contain mostly small to moderate effect sizes, but a few studies examined large effect sizes. To simulated skewed effect size distributions, I used the rsnorm function of the fGarch package. The function creates a random distribution with a specified mean, standard deviation, and skew. I set the mean to d = .2, the standard deviation to SD = .2, and skew to 2. The histograms show the distribution of effect sizes and the distribution of true power for the 5,000 sets of studies (k = 10).

This time the results show differences between estimation methods in the ability of various estimation methods to deal with skewed heterogeneity. The percentage of significant results is unbiased, but is imprecise due to the problem of averaging dichotomous variables. The other methods show systematic deviations from the 95% confidence interval around the true parameter. Visual inspection suggests that the Yuan-Maxwell correction method has the best fit.

This impression is confirmed in quantitative analyses of bias. The quantitative comparison confirms major problems with the puniform estimation method. It also shows that the median, p-curve, and the average z-score method have the same slight positive bias. Only the Yuan-Maxwell corrected average power shows little systematic bias.

To examine biases in more detail, the following graphs plot bias as a function of true power. These plots can reveal that a method may have little average bias, but has different types of bias for different levels of power. The results show little evidence of systematic bias for the Yuan-Maxwell corrected average of power.

The following analyses examined bias separately for simulation with less or more than 50% true power. The results confirm that all methods except the Yuan-Maxwell correction underestimate power when true power is below 50%. In contrast, most estimation methods overestimate true power when true power is above 50%. The exception is puniform which still underestimated true power. More research needs to be done to understand the strange performance of puniform in this simulation. However, even if p-uniform could perform better, it is likely to be biased with skewed distributions of effect sizes because it assumes a fixed population effect size.

Conclusion

This investigation introduced and compared different methods to estimate true power for a set of studies. All estimation methods performed well when a set of studies had the same true power (exact replication studies), when effect sizes were homogenous and sample sizes varied, and when effect sizes were normally distributed and sample sizes were fixed. However, most estimation methods were systematically biased when the distribution of effect sizes was skewed. In this situation, most methods run into problems because the percentage of significant results is a function of the power of individual studies rather than the average power.

The results of these analyses suggest that the R-Index (Schimmack, 2014) can be improved by simply averaging power and then applying the Yuan-Maxwell correction. However, it is important to realize that the median method tends to overestimate power when power is greater than 50%. This makes it even more difficult for the R-Index to produce an estimate of low power when power is actually high. The next step in the investigation of observed power is to examine how different methods perform in unrepresentative (biased) sets of studies. In this case, the percentage of significant results is highly misleading. For example, Sterling et al. (1995) found percentages of 95% power, which would suggest that studies had 95% power. However, publication bias and questionable research practices create a bias in the sample of studies that are being published in journals. The question is whether other observed power estimates can reveal bias and can produce accurate estimates of the true power in a set of studies.

An Introduction to Observed Power based on Yuan and Maxwell (2005)

March 24, 2015Introduction, Observed Power, Post-Hoc Power, Power, Statistics, Yuan and MaxwellBias, Median Observed Power, Meta-Analysis, Observed Power, Post-hoc Power, Power, Statistics, Yuan and MaxwellUlrich Schimmack

Yuan, K.-H., & Maxwell, S. (2005). On the Post Hoc Power in Testing Mean Differences. Journal of Educational and Behavioral Statistics, 141–167

This blog post provides an accessible introduction to the concept of observed power. Most of the statistical points are based on based on Yuan and Maxwell’s (2005 excellent but highly technical article about post-hoc power. This bog post tries to explain statistical concepts in more detail and uses simulation studies to illustrate important points.

What is Power?

Power is defined as the long-run probability of obtaining significant results in a series of exact replication studies. For example, 50% power means that a set of 100 studies is expected to produce 50 significant results and 50 non-significant results. The exact numbers in an actual set of studies will vary as a function of random sampling error, just like 100 coin flips are not always going to produce a 50:50 split of heads and tails. However, as the number of studies increases, the percentage of significant results will be ever closer to the power of a specific study.

A priori power

Power analysis can be useful for the planning of sample sizes before a study is being conducted. A power analysis that is being conducted before a study is called a priori power analysis (before = a priori). Power is a function of three parameters: the actual effect size, sampling error, and the criterion value that needs to be exceeded to claim statistical significance. In between-subject designs, sampling error is determined by sample size alone. In this special case, power is a function of the true effect size, the significance criterion and sample size.

The problem for researchers is that power depends on the effect size in the population (e.g., the true correlation between height and weight amongst Canadians in 2015). The population effect size is sometimes called the true effect size. Imagine that somebody would actually obtain data from everybody in a population. In this case, there is no sampling error and the correlation is the true correlation in the population. However, typically researchers use much smaller samples and the goal is to estimate the correlation in the population on the basis of a smaller sample. Unfortunately, power depends on the correlation in the population, which is unknown to a researcher planning a study. Therefore, researchers have to estimate the true effect size to compute an a priori power analysis.

Cohen (1988) developed general guidelines for the estimation of effect sizes. For example, in studies that compare the means of two groups, a standardized difference of half a standard deviation (e.g., 7.5 IQ points on an iQ scale with a standard deviation of 15) is considered a moderate effect. Researchers who assume that their predicted effect has a moderate effect size, can use d = .5 for an a priori power analysis. Assuming that they want to claim significance with the standard criterion of p < .05 (two-tailed), they would need N = 210 (n =105 per group) to have a 95% chance to obtain a significant result (GPower). I do not discuss a priori power analysis further because this blog post is about observed power. I merely introduced a priori power analysis to highlight the difference between a priori power analysis and a posteriori power analysis, which is the main topic of Yuan and Maxwell’s (2005) article.

A Posteriori Power Analysis: Observed Power

Observed power computes power after a study or several studies have been conducted. The key difference between a priori and a posteriori power analysis is that a posteriori power analysis uses the observed effect size in a study as an estimate of the population effect size. For example, assume a researcher found a correlation of r = .54 in a sample of N = 200 Canadians. Instead of guessing the effect size, the researcher uses the correlation observed in this sample as an estimate of the correlation in the population. There are several reasons why it might be interesting to conduct a power analysis after a study. First, the power analysis might be used to plan a follow up or replication study. Second, the power analysis might be used to examine whether a non-significant result might be the result of insufficient power. Third, observed power is used to examine whether a researcher used questionable research practices to produce significant results in studies that had insufficient power to produce significant results.

In sum, observed power is an estimate of the power of a study based on the observed effect size in a study. It is therefore not power that is being observed, but the effect size that is being observed. However, because the other parameters that are needed to compute power are known (sample size, significance criterion), the observed effect size is the only parameter that needs to be observed to estimate power. However, it is important to realize that observed power does not mean that power was actually observed. Observed power is still an estimate based on an observed effect size because power depends on the effect size in the population (which remains unobserved) and the observed effect size in a sample is just an estimate of the population effect size.

A Posteriori Power Analysis after a Single Study

Yuan and Maxwell (2005) examined the statistical properties of observed power. The main question was whether it is meaningful to compute observed power based on the observed effect size in a single study.

The first statistical analysis of an observed mean difference is to examine whether the study produced a significant result. For example, the study may have examined whether music lessons produce an increase in children’s IQ. The study had 95% power to produce a significant difference with N = 176 participants and a moderate effect size (d = .5; IQ = 7.5).

One possibility is that the study actually produced a significant result. For example, the observed IQ difference was 5 IQ points. This is less than the expected difference of 7.5 points and corresponds to a standardized effect size of d = .3. Yet, the t-test shows a highly significant difference between the two groups, t(208) = 3.6, p = 0.0004 (1 / 2513). The p-value shows that random sampling error alone would produce differences of this magnitude or more in only 1 out of 2513 studies. Importantly, the p-value only makes it very likely that the intervention contributed to the mean difference, but it does not provide information about the size of the effect. The true effect size may be closer to the expected effect size of 7.5 or it may be closer to 0. The true effect size remains unknown even after the mean difference between the two groups is observed. Yet, the study provides some useful information about the effect size. Whereas the a priori power analysis relied exclusively on guess-work, observed power uses the effect size that was observed in a reasonably large sample of 210 participants. Everything else being equal, effect size estimates based on 210 participants are more likely to match the true effect size than those based on 0 participants.

The observed effect size can be entered into a power analysis to compute observed power. In this example, observed power with an effect size of d = .3 and N = 210 (n = 105 per group) is 58%. One question examined by Yuan and Maxwell (2005) is whether it can be useful to compute observed power after a study produced a significant result.

The other question is whether it can be useful to compute observed power when a study produced a non-significant result. For example, assume that the estimate of d = 5 is overly optimistic and that the true effect size of music lessons on IQ is a more modest 1.5 IQ points (d = .10, one-tenth of a standard deviation). The actual mean difference that is observed after the study happens to match the true effect size exactly. The difference between the two groups is not statistically significant, t(208) = .72, p = .47. A non-significant result is difficult to interpret. On the one hand, the means trend in the right direction. On the other hand, the mean difference is not statistically significant. The p-value suggests that a mean difference of this magnitude would occur in every second study by chance alone even if music intervention had no effect on IQ at all (i.e., the true effect size is d = 0, the null-hypothesis is true). Statistically, the correct conclusion is that the study provided insufficient information regarding the influence of music lessons on IQ. In other words, assuming that the true effect size is closer to the observed effect size in a sample (d = .1) than to the effect size that was used to plan the study (d = .5), the sample size was insufficient to produce a statistically significant result. Computing observed power merely provides some quantitative information to reinforce this correct conclusion. An a posteriori power analysis with d = .1 and N = 210, yields an observed power of 11%. This suggests that the study had insufficient power to produce a significant result, if the effect size in the sample matches the true effect size.

Yuan and Maxwell (2005) discuss false interpretations of observed power. One false interpretation is that a significant result implies that a study had sufficient power. Power is a function of the true effect size and observed power relies on effect sizes in a sample. 50% of the time, effect sizes in a sample overestimate the true effect size and observed power is inflated. It is therefore possible that observed power is considerably higher than the actual power of a study.

Another false interpretation is that low power in a study with a non-significant result means that the hypothesis is correct, but that the study had insufficient power to demonstrate it. The problem with this interpretation is that there are two potential reasons for a non-significant result. One of them, is that a study had insufficient power to show a significant result when an effect is actually present (this is called the type-II error). The second possible explanation is that the null-hypothesis is actually true (there is no effect). A non-significant result cannot distinguish between these two explanations. Yet, it remains true that the study had insufficient power to test these hypotheses against each other. Even if a study had 95% power to show an effect if the true effect size is d = .5, it can have insufficient power if the true effect size is smaller. In the example, power decreased from 95% assuming d = .5, to 11% assuming d = .1.

Yuan and Maxell’s Demonstration of Systematic Bias in Observed Power

Yuan and Maxwell focus on a design in which a sample mean is compared against a population mean and the standard deviation is known. To modify the original example, a researcher could recruit a random sample of children, do a music lesson intervention and test the IQ after the intervention against the population mean of 100 with the population standard deviation of 15, rather than relying on the standard deviation in a sample as an estimate of the standard deviation. This scenario has some advantageous for mathematical treatments because it uses the standard normal distribution. However, all conclusions can be generalized to more complex designs. Thus, although Yuan and Maxwell focus on an unusual design, their conclusions hold for more typical designs such as the comparison of two groups that use sample variances (standard deviations) to estimate the variance in a population (i.e., pooling observed variances in both groups to estimate the population variance).

Yuan and Maxwell (2005) also focus on one-tailed tests, although the default criterion in actual studies is a two-tailed test. Once again, this is not a problem for their conclusions because the two-tailed criterion value for p = .05 is equivalent to the one-tailed criterion value for p = .025 (.05 / 2). For the standard normal distribution, the value is z = 1.96. This means that an observed z-score has to exceed a value of 1.96 to be considered significant.

To illustrate this with an example, assume that the IQ of 100 children after a music intervention is 103. After subtracting the population mean of 100 and dividing by the standard deviation of 15, the effect size is d = 3/15 = .2. Sampling error is defined by 1 / sqrt (n). With a sample size of n = 100, sampling error is .10. The test-statistic (z) is the ratio of the effect size and sampling error (.2 / .1) = 2. A z-score of 2 is just above the critical value of 2, and would produce a significant result, z = 2, p = .023 (one-tailed; remember criterion is .025 one-tailed to match .05 two-tailed). Based on this result, a researcher would be justified to reject the null-hypothesis (there is no effect of the intervention) and to claim support for the hypothesis that music lessons lead to an increase in IQ. Importantly, this hypothesis makes no claim about the true effect size. It merely states that the effect is greater than zero. The observed effect size in the sample (d = .2) provides an estimate of the actual effect size but the true effect size can be smaller or larger than the effect size in the sample. The significance test merely rejects the possibility that the effect size is 0 or less (i.e., music lessons lower IQ).

Entering a non-centrality parameter of 3 for a generic z-test in G*power yields the following illustration of a non-central distribution.

Illustration of non-central distribution using G*Power output

The red curve shows the standard normal distribution for the null-hypothesis. With d = 0, the non-centrality parameter is also 0 and the standard normal distribution is centered over zero.

The blue curve shows the non-central distribution. It is the same standard normal distribution, but now it is centered over z = 3. The distribution shows how z-scores would be distributed for a set of exact replication studies, where exact replication studies are defined as studies with the same true effect size and sampling error.

The figure also illustrates power by showing the critical z-score of 1.96 with a green line. On the left side are studies where sampling error reduced the observed effect size so much that the z-score was below 1.96 and produced a non-significant result (p > .025 one-tailed, p > .05, two-tailed). On the right side are studies with significant results. The area under the curve on the left side is called type-II error or beta-error). The area under the curve on the right side is called power (1 – type-II error). The output shows that beta error probability is 15% and Power is 85%.

In sum, the formula

states that power for a given true effect size is the area under the curve to the right side of a critical z-score for a standard normal distribution that is centered over the non-centrality parameter that is defined by the ratio of the true effect size over sampling error.

[personal comment: I find it odd that sampling error is used on the right side of the formula but not on the left side of the formula. Power is a function of the non-centrality parameter and not just the effect size. Thus I would have included sqrt (n) also on the left side of the formula].

Because the formula relies on the true effect size, it specifies true power given the (unknown) population effect size. To use it for observed power, power has to be estimated based on the observed effect size in a sample.

The important novel contribution of Yuan and Maxwell (2005) was to develop a mathematical formula that relates observed power to true power and to find a mathematical formula for the bias in observed power.

The formula implies that the amount of bias is a function of the unknown population effect size. Yuan and Maxwell make several additional observations about bias. First, bias is zero when true power is 50%. The second important observation is that systematic bias is never greater than 9 percentage points. The third observation is that power is overestimated when true power is less than 50% and underestimated when true power is above 50%. The last observation has important implications for the interpretation of observed power.

50% power implies that the test statistic matches the criterion value. For example, if the criterion is p < .05 (two-tailed), 50% power is equivalent to p = .05. If observed power is less than 50%, a study produced a non-significant result. A posteriori power analysis might suggest that observed power is only 40%. This finding suggests that the study was underpowered and that a more powerful study might produce a significant result. Systematic bias implies that the estimate of 40% is more likely to be an overestimation than an underestimation. As a result, bias does not undermine the conclusion. Rather observed power is conservative because the actual power is likely to be even less than 40%.

The alternative scenario is that observed power is greater than 50%, which implies a significant result. In this case, observed power might be used to argue that a study had sufficient power because it did produce a significant result. Observed power might show, however, that observed power is only 60%. This would indicate that there was a relatively high chance to end up with a non-significant result. However, systematic bias implies that observed power is more likely to underestimate true power than to overestimate it. Thus, true power is likely to be higher. Again, observed power is conservative when it comes to the interpretation of power for studies with significant results. This would suggest that systematic bias is not a serious problem for the use of observed power. Moreover, the systematic bias is never more than 9 percentage-points. Thus, observed power of 60% cannot be systematically inflated to more than 70%.

In sum, Yuan and Maxwell (2005) provided a valuable analysis of observed power and demonstrated analytically the properties of observed power.

Practical Implications of Yuan and Maxwell’s Findings

Based on their analyses, Yuan and Maxwell (2005) draw the following conclusions in the abstract of their article.

Using analytical, numerical, and Monte Carlo approaches, our results show that the estimated power does not provide useful information when the true power is small. It is almost always a biased estimator of the true power. The bias can be negative or positive. Large sample size alone does not guarantee the post hoc power to be a good estimator of the true power.

Unfortunately, other scientists often only read the abstract, especially when the article contains mathematical formulas that applied scientists find difficult to follow. As a result, Yuan and Maxwell’s (2005) article has been cited mostly as evidence that it observed power is a useless concept. I think this conclusion is justified based on Yuan and Maxwell’s abstract, but it does not follow from Yuan and Maxwell’s formula of bias. To make this point, I conducted a simulation study that paired 25 sample sizes (n = 10 to n = 250) and 20 effect sizes (d = .05 to d = 1) to create 500 non-centrality parameters. Observed effect sizes were randomly generated for a between-subject design with two groups (df = n*2 – 2). For each non-centrality parameter, two simulations were conducted for a total of 1000 studies with heterogeneous effect sizes and sample sizes (standard errors). The results are presented in a scatterplot with true power on the x-axis and observed power on the y-axis. The blue line shows prediction of observed power from true power. The red curve shows the biased prediction based on Yuan and Maxwell’s bias formula.

The most important observation is that observed power varies widely as a function of random sampling error in the observed effect sizes. In comparison, the systematic bias is relatively small. Moreover, observed power at the extremes clearly distinguishes between low powered (< 25%) and high powered (> 80%) power. Observed power is particularly informative when it is close to the maximum value of 100%. Thus, observed power of 99% or more strongly suggests that a study had high power. The main problem for posteriori power analysis is that observed effect sizes are imprecise estimates of the true effect size, especially in small samples. The next section examines the consequences of random sampling error in more detail.

Standard Deviation of Observed Power

Awareness has been increasing that point estimates of statistical parameters can be misleading. For example, an effect size of d = .8 suggests a strong effect, but if this effect size was observed in a small sample, the effect size is strongly influenced by sampling error. One solution to this problem is to compute a confidence interval around the observed effect size. The 95% confidence interval is defined by sampling error times 1.96; approximately 2. With sampling error of .4, the confidence interval could range all the way from 0 to 1.6. As a result, it would be misleading to claim that an effect size of d = .8 in a small sample suggests that the true effect size is strong. One solution to this problem is to report confidence intervals around point estimates of effect sizes. A common confidence interval is the 95% confidence interval. A 95% confidence interval means that there is a 95% probability that the population effect size is contained in the 95% confidence interval around the (biased) effect size in a sample.

To illustrate the use of confidence interval, I computed the confidence interval for the example of music training and IQ in children. The example assumes that the IQ of 100 children after a music intervention is 103. After subtracting the population mean of 100 and dividing by the standard deviation of 15, the effect size is d = 3/15 = .2. Sampling error is defined by 1 / sqrt (n). With a sample size of n = 100, sampling error is .10. To compute a 95% confidence interval, sampling error is multiplied with the z-scores that capture 95% of a standard normal distribution, which is 1.96. As sampling error is .10, the values are -.196 and .196. Given an observed effect size of d = .2, the 95% confidence interval ranges from .2 – .196 = .004 to .2 + .196 = .396.

A confidence interval can be used for significance testing by examining whether the confidence interval includes 0. If the 95% confidence interval does not include zero, it is possible to reject the hypothesis that the effect size in the population is 0, which is equivalent to rejecting the null-hypothesis. In the example, the confidence interval ends at d = .004, which implies that the null-hypothesis can be rejected. At the upper end, the confidence interval ends at d = .396. This implies that the empirical results also would reject hypotheses that the population effect size is moderate (d = .5) or strong (d = .8).

Confidence intervals around effect sizes are also useful for posteriori power analysis. Yuan and Maxwell (2005) demonstrated that confidence interval of observed power is defined by the observed power of the effect sizes that define the confidence interval of effect sizes.

The figure below illustrates the observed power for the lower bound of the confidence interval in the example of music lessons and IQ (d = .004).

The figure shows that the non-central distribution (blue) and the central distribution (red) nearly perfectly overlap. The reason is that the observed effect size (d = .004) is just slightly above the d-value of the central distribution when the effect size is zero (d = .000). When the null-hypothesis is true, power equals the type-I error rate (2.5%) because 2.5% of studies will produce a significant result by chance alone and chance is the only factor that produces significant results. When the true effect size is d = .004, power increases to 2.74 percent.

Remember that this power estimate is based on the lower limit of a 95% confidence interval around the observed power estimate of 50%. Thus, this result means that there is a 95% probability that the true power of the study is 2.5% when observed power is 50%.

The next figure illustrates power for the upper limit of the 95% confidence interval.

In this case, the non-central distribution and the central distribution overlap very little. Only 2.5% of the non-central distribution is on the left side of the criterion value, and power is 97.5%. This finding means that there is a 95% probability that true power is not greater than 97.5% when observed power is 50%.

Taken these results together, the results show that the 95% confidence interval around an observed power estimate of 50% ranges from 2.5% to 97.5%. As this interval covers pretty much the full range of possible values, it follows that observed power of 50% in a single study provides virtually no information about the true power of a study. True power can be anywhere between 2.5% and 97.5% percent.

The next figure illustrates confidence intervals for different levels of power.

The data are based on the same simulation as in the previous simulation study. The green line is based on computation of observed power for the d-values that correspond to the 95% confidence interval around the observed (simulated) d-values.

The figure shows that confidence intervals for most observed power values are very wide. The only accurate estimate of observed power can be achieved when power is high (upper right corner). But even 80% true power still has a wide confidence interval where the lower bound is below 20% observed power. Firm conclusions can only be drawn when observed power is high.

For example, when observed power is 95%, a one-sided 95% confidence interval (guarding only against underestimation) has a lower bound of 50% power. This finding would imply that observing power of 95% justifies the conclusion that the study had at least 50% power with an error rate of 5% (i.e., in 5% of the studies the true power is less than 50%).

The implication is that observed power is useless unless observed power is 95% or higher.

In conclusion, consideration of the effect of random sampling error on effect size estimates provides justification for Yuan and Maxwell’s (2005) conclusion that computation of observed power provides relatively little value. However, the reason is not that observed power is a problematic concept. The reason is that observed effect sizes in underpowered studies provide insufficient information to estimate observed power with any useful degree of accuracy. The same holds for the reporting of observed effect sizes that are routinely reported in research reports and for point estimates of effect sizes that are interpreted as evidence for small, moderate, or large effects. None of these statements are warranted when the confidence interval around these point estimates is taken into account. A study with d = .80 and a confidence interval of d = .01 to 1.59 does not justify the conclusion that a manipulation had a strong effect because the observed effect size is largely influenced by sampling error.

In conclusion, studies with large sampling error (small sample sizes) are at best able to determine the sign of a relationship. Significant positive effects are likely to be positive and significant negative effects are likely to be negative. However, the effect sizes in these studies are too strongly influenced by sampling error to provide information about the population effect size and therewith about parameters that depend on accurate estimation of population effect sizes like power.

Meta-Analysis of Observed Power

One solution to the problem of insufficient information in a single underpowered study is to combine the results of several underpowered studies in a meta-analysis. A meta-analysis reduces sampling error because sampling error creates random variation in effect size estimates across studies and aggregation reduces the influence of random factors. If a meta-analysis of effect sizes can produce more accurate estimates of the population effect size, it would make sense that meta-analysis can also increase the accuracy of observed power estimation.

Yuan and Maxwell (2005) discuss meta-analysis of observed power only briefly.

A problem in a meta-analysis of observed power is that observed power is not only subject to random sampling error, but also systematically biased. As a result, the average of observed power across a set of studies would also be systematically biased. However, the reason for the systematic bias is the non-symmetrical distribution of observed power when power is not 50%. To avoid this systematic bias, it is possible to compute the median. The median is unbiased because 50% of the non-central distribution is on the left side of the non-centrality parameter and 50% is on the right side of the non-centrality parameter. Thus, the median provides an unbiased estimate of the non-centrality parameter and the estimate becomes increasingly accurate as the number of studies in a meta-analysis increases.

The next figure shows the results of a simulation with the same 500 studies (25 sample sizes and 20 effect sizes) that were simulated earlier, but this time each study was simulated to be replicated 1,000 times and observed power was estimated by computing the average or the median power across the 1,000 exact replication studies.

Purple = average observed power; Orange = median observed power

The simulation shows that Yuan and Maxwell’s (2005) bias formula predicts the relationship between true power and the average of observed power. It also confirms that the median is an unbiased estimator of true power and that observed power is a good estimate of true power when the median is based on a large set of studies. However, the question remains whether observed power can estimate true power when the number of studies is smaller.

The next figure shows the results for a simulation where estimated power is based on the median observed power in 50 studies. The maximum discrepancy in this simulation was 15 percentage points. This is clearly sufficient to distinguish low powered studies (<50% power) from high powered studies (>80%).

To obtain confidence intervals for median observed power estimates, the power estimate can be converted into the corresponding non-centrality parameter of a standard normal distribution. The 95% confidence interval is defined as the standard deviation divided by the square root of the number of studies. The standard deviation of a standard normal distribution equals 1. Hence, the 95% confidence interval for a set of studies is defined by

Lower Limit = Normal (InverseNormal (power) – 1.96 / sqrt(k))

Upper Limit = Normal (inverseNormal(power) + 1.96 / sqrt(k))

Interestingly, the number of observations in a study is irrelevant. The reason is that larger samples produce smaller confidence intervals around an effect size estimate and increase power at the same time. To hold power constant, the effect size has to decrease and power decreases exponentially as effect sizes decrease. As a result, observed power estimates do not become more precise when sample sizes increase and effect sizes decrease proportionally.

The next figure shows simulated data for 1000 studies with 20 effect sizes (0.05 to 1) and 25 sample sizes (n = 10 to 250). Each study was repeated 50 times and the median value was used to estimate true power. The green lines are the 95% confidence interval around the true power value. In real data, the confidence interval would be drawn around observed power, but observed power does not provide a clear mathematical function. The 95% confidence interval around the true power values is still useful because it predicts how much observed power estimates can deviate from true power. 95% of observed power values are expected to be within the area that is defined by lower and upper bound of the confidence interval. The Figure shows that most values are within the area. This confirms that sampling error in a meta-analysis of observed power is a function of the number of studies. The figure also shows that sampling error is greatest when power is 50%. In the tails of the distribution range restriction produces more precise estimates more quickly.

With 50 studies, the maximum absolute discrepancy is 15 percentage points. This level of precision is sufficient to draw broad conclusions about the power of a set of studies. For example, any median observed power estimate below 65% is sufficient to reveal that a set of studies had less power than Cohen’s recommended level of 80% power. A value of 35% would strongly suggest that a set of studies was severely underpowered.

Conclusion

Yuan and Maxwell (2005) provided a detailed statistical examination of observed power. They concluded that observed power typically provides little to no useful information about the true power of a single study. The main reason for this conclusion was that sampling error in studies with low power is too large to estimate true power with sufficient precision. The only precise estimate of power can be obtained when sampling error is small and effect sizes are large. In this case, power is near the maximum value of 1 and observed power correctly estimates true power as being close to 1. Thus, observed power can be useful when it suggests that a study had high power.

Yuan and Maxwell’s (2005) also showed that observed power is systematically biased unless true power is 50%. The amount of bias is relatively small and even without this systematic bias, the amount of random error is so large that observed power estimates based on a single study cannot be trusted.

Unfortunately, Yuan and Maxwell’s (2005) article has been misinterpreted as evidence that observed power calculations are inherently biased and useless. However, observed power can provide useful and unbiased information in a meta-analysis of several studies. First, a meta-analysis can provide unbiased estimates of power because the median value is an unbiased estimator of power. Second, aggregation across studies reduces random sampling error, just like aggregation across studies reduces sampling error in meta-analyses of effect sizes.

Implications

The demonstration that median observed power provides useful information about true power is important because observed power has become a valuable tool in the detection of publication bias and other biases that lead to inflated estimates of effect sizes. Starting with Sterling, Rosenbaum, and Weinkam ‘s(1995) seminal article, observed power has been used by Ioannidis and Trikalinos (2007), Schimmack (2012), Francis (2012), Simonsohn (2014), and van Assen, van Aert, and Wicherts (2014) to draw inferences about a set of studies with the help of posteriori power analysis. The methods differ in the way observed data are used to estimate power, but they all rely on the assumption that observed data provide useful information about the true power of a set of studies. This blog post shows that Yuan and Maxwell’s (2005) critical examination of observed power does not undermine the validity of statistical approaches that rely on observed data to estimate power.

Future Directions

This blog post focussed on meta-analysis of exact replication studies that have the same population effect size and the same sample size (sampling error). It also assumed that the set of studies is a representative set of studies. An important challenge for future research is to examine the statistical properties of observed power when power varies across studies (heterogeneity) and when publication bias and other biases are present. A major limitation of existing methods is that these methods assume a fixed population effect size (Ioannidis and Trikalinos (2007), Francis (2012), Simonsohn (2014), and van Assen, van Aert, and Wicherts (2014). At present, the Incredibility index (Schimmack, 2012) and the R-Index (Schimmack, 2014) have been proposed as methods for sets of studies that are biased and heterogeneous. An important goal for future research is to evaluate these methods in simulation studies with heterogeneous and biased sets of data.

Power Failure in Neuroscience

December 5, 2014Button, Ioannidis, Nosek, Observed Power, Post-Hoc Power, Power, Power Failure, scienceNature Neuroscience, r-index, replicabilityUlrich Schimmack

Original: December 5, 2014
Revised: December 28, 2020

Power Failure in Neuroscience

An article in Nature Review” Neuroscience suggested that the median power in neuroscience studies is just 21% (Katherine S. Button, John P. A. Ioannidis, Claire Mokrysz, Brian A.Nosek, Jonathan Flint, Emma S.J. Robinson and Marcus R. Munafò, 2013).

The authors of this article examined meta-analyses of primary studies in neuroscience that were published in 2011. They analyzed 49 meta-analyses that were based on a total of 730 original studies (on average, 15 studies per meta-analysis, range 2 to 57).

For each primary study, the authors computed observed power based on the sample size and the estimated effect size in the meta-analysis.

Based on their analyses, the authors concluded that the median power in neuroscience is 21%.

There is a major problem with this estimate that the authors overlooked. The power estimate is incredibly low because a median power estimate of 21% corresponds to a p-value of p = .25. If median power were 21%, it would mean that over 50% of the original studies in the meta-analysis reported a non-significant result (p > .05). This seems rather unlikely because journals tend to publish mostly significant results.

The estimate is even less plausible because it is based on meta-analytic averages without any correction for bias. These effect sizes are likely to be inflated, which means that median power estimate is inflated. Thus, true power is even less than 21% and even more results are non-significant.

What could explain this implausible result?

A meta-analysis includes published and unpublished studies. It is possible that the published studies reported significant results with observed power greater than 50% (p < .05) and the unpublished studies reported non-significant results with power less than 50%. However, this would imply that meta-analysts were able to retrieve as many unpublished studies as published studies. The authors did not report whether power of published and unpublished studies differed.
A second possibility is that the power analyses produced false results. The authors relied on Ioannidis and Trikalinos’s (2007) approach to the estimation of power. This approach assumes that studies in a meta-analysis have the same true effect size and that the meta-analytic average (weighted mean) provides the best estimate of the true effect size. This estimate of the true effect size is then used to estimate power in individual studies based on the sample size of the study. As already noted by Ioannidis and Trikalinos (2007), this approach can produce biased results when effect sizes in a meta-analysis are heterogeneous.
Estimating power simply on the basis of effect size and sample size can be misleading when the design is not a simple comparison of two groups. Between-subject designs are common in animal studies in neuroscience. However, many fMRI studies use within-subject designs that achieve high statistical power with a few participants because participants serve as their own controls.

Schimmack (2012) proposed an alternative procedure that does not have this limitation. Power is estimated individually for each study based on the observed effect size in this study. This approach makes it possible to estimate median power for heterogeneous sets of studies with different effect sizes. Moreover, this approach makes it possible to compute power when power is not simply a function of sample size and effect size (e.g., within-subject designs).

R-Index of Nature Neuroscience: Analysis

To examine the replicability of research published in nature and neuroscience, I retrieved the most cited articles in this journal until I had a sample of 20 studies. I needed 14 articles to meet this goal. The number of studies in these articles ranged from 1 to 7.

The success rate for focal significance tests was 97%. This implies that the vast majority of significance tests reported a significant result. The median observed power was 84%. The inflation rate is 13% (97% – 84% = 13%). The R-Index is 71%. Based on these numbers, the R-Index predicts that the majority of studies in nature neuroscience would replicate in an exact replication study.

This conclusion differs dramatically from Button et al.’s (2013) conclusion. I therefore examined some of the articles that were used for Button et al.’s analyses.

A study by Davidson et al. (2003) examined treatment effects in 12 depressed patients and compared them to 5 healthy controls. The main findings in this article were three significant interactions between time of treatment and group with z-scores of 3.84, 4.60, and 4.08. Observed power for these values with p = .05 is over 95%. If a more conservative significance level of p = .001 is used, power is still over 70%. However, the meta-analysis focused on the correlation between brain activity at baseline and changes in depression over time. This correlation is shown with a scatterplot without reporting the actual correlation or testing it for significance. The text further states that a similar correlation was observed for an alternative depression measure with r = .46 and noting correctly that this correlation is not significant, t(10) = 1.64, p = .13, d = .95, obs. power = 32%. The meta-analysis found a mean effect size of .92. A power analysis with d = .92 and N = 12 yields a power estimate of 30%. Presumably, this is the value that Button et al. used to estimate power for the Davidson et al. (2003) article. However, the meta-analysis did not include the more powerful analyses that compared patients and controls over time.

Conclusion

In the current replication crisis, there is a lot of confusion about the replicability of published findings. Button et al. (2013) aimed to provide some objective information about the replicability of neuroscience research. They concluded that replicability is very low with a median estimate of 21%. In this post, I point out some problems with their statistical approach and the focus on meta-analyses as a way to make inferences about replicability of published studies. My own analysis shows a relatively high R-Index of 71%. To make sense of this index it is instructive to compare it to the following R-Indices.

In a replication project of psychological studies, I found an R-Index of 43% and 28% of studies were successfully replicated.

In the many-labs replication project, 10 out of 12 studies were successfully replicated, a replication rate of 83% and the R-Index was 72%.

Caveat

Neuroscience studies may have high observed power and still not replicate very well in exact replications. The reason is that measuring brain activity is difficult and requires many steps to convert and reduce observed data into measures of brain activity in specific regions. Actual replication studies are needed to examine the replicability of published results.

The Replicability-Index (R-Index): Quantifying Research Integrity

December 1, 2014Post-Hoc Power, r-index, R-Index4Science, Replicability, Research Integrity, scienceForensic Statistics, Questionable Research Practices, research integrity, scientific integrity, Scientific MisonductUlrich Schimmack

ANNIVERSARY POST. Slightly edited version of first R-Index Blog on December 1, 2014.

In a now infamous article, Bem (2011) produced 9 (out of 10) statistically significant results that appeared to show time-reversed causality. Not surprisingly, subsequent studies failed to replicate this finding. Although Bem never admitted it, it is likely that he used questionable research practices to produce his results. That is, he did not just run 10 studies and found 9 significant results. He may have dropped failed studies, deleted outliers, etc. It is well-known among scientists (but not lay people) that researchers routinely use these questionable practices to produce results that advance their careers. Think, doping for scientists.

I have developed a statistical index that tracks whether published results were obtained by conducting a series of studies with a good chance of producing a positive result (high statistical power) or whether researchers used questionable research practices. The R-Index is a function of the observed power in a set of studies. More power means that results are likely to replicate in a replication attempt. The second component of the R-index is the discrepancy between observed power and the rate of significant results. 100 studies with 80% power should produce, on average, 80% significant results. If observed power is 80% and the success rate is 100%, questionable research practices were used to obtain more significant results than the data justify. In this case, the actual power is less than 80% because questionable research practices inflate observed power. The R-index subtracts the discrepancy (in this case 20% too many significant results) from observed power to adjust for the inflation. For example, if observed power is 80% and success rate is 100%, the discrepancy is 20% and the R-index is 60%.

In a paper, I show that the R-index predicts success in empirical replication studies.

The R-index also sheds light on the recent controversy about failed replications in psychology (repligate) between replicators and “replihaters.” Replicators sometimes imply that failed replications are to be expected because original studies used small samples with surprisingly large effects, possibly due to the use of questionable research practices. Replihaters counter that replicators are incompetent researchers who are motivated to produce failed studies. The R-Index makes it possible to evaluate these claims objectively and scientifically. It shows that the rampant use of questionable research practices in original studies makes it extremely likely that replication studies will fail. Replihaters should take note that questionable research practices can be detected and that many failed replications are predicted by low statistical power in original articles.