2021
DOI: 10.1037/met0000337
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Power contours: Optimising sample size and precision in experimental psychology and human neuroscience.

Abstract: When designing experimental studies with human participants, experimenters must decide how many trials each participant will complete, as well as how many participants to test. Most discussion of statistical power (the ability of a study design to detect an effect) has focused on sample size, and assumed sufficient trials. Here we explore the influence of both factors on statistical power, represented as a 2-dimensional plot on which iso-power contours can be visualized. We demonstrate the conditions under whi… Show more

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Cited by 190 publications
(170 citation statements)
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“…Increasing the number of repetitions per condition can be applied for all diagnostic assessment procedures with homogeneous items. The role of the number of trials in experimental psychology tasks has been recently raised as an important factor to be considered to ensure sufficient power (Baker et al, 2019;Brysbaert, 2019). When more trials are included for averaging, the errors associated with the single measurements tend to cancel each other out more accurately 16 .…”
Section: Improving Snarc Effect Reliability and Precisionmentioning
confidence: 99%
“…Increasing the number of repetitions per condition can be applied for all diagnostic assessment procedures with homogeneous items. The role of the number of trials in experimental psychology tasks has been recently raised as an important factor to be considered to ensure sufficient power (Baker et al, 2019;Brysbaert, 2019). When more trials are included for averaging, the errors associated with the single measurements tend to cancel each other out more accurately 16 .…”
Section: Improving Snarc Effect Reliability and Precisionmentioning
confidence: 99%
“…From this perspective, power should be calculated for effects within individual participants. This gives a very different view of the strength of evidence provided by a data set and of the importance of sample size (for both participants and trials) compared to the more common population mean perspective (Baker et al, 2019). For example, the simulation of 50 participants with 20 trials in Figure 1C has = 0.008 for a group mean different from zero, a result that is as surprising, under the null hypothesis, as observing 7 heads in a row from tosses of a fair coin (Obleser, 2019).…”
Section: Discussionmentioning
confidence: 99%
“…Figure 2A-C suggests that for the Bayesian prevalence metrics, there are benefits to having larger numbers of participants (decrease in variance of obtained MAP and HPDI width, increase in prevalence lower bound), but beyond around 50 participants these benefits become less pronounced. Figures 2E shows that inferred prevalence is mostly sensitive to the number of trials per participant (horizontal contours), and invariant to the number of participants (although variance increases as in Figure 2A,C,F), whereas t-test power ( Figure 2D) is mostly sensitive to number of participants (vertical contours) and largely invariant to number of trials beyond around 100 trials per participant (Baker et al, 2019). In sum, compared to the population mean t-test, prevalence exhibits greater sensitivity to the number of trials obtained per participant, and less sensitivity to the number of participants.…”
Section: Estimating Population Prevalencementioning
confidence: 93%
“…Their focus is on comparing between different decision models rather than model-free and model-based transformations of reaction time and accuracy. Baker et al (2019) used the simulation method to address a question of equal importance to experimentalists-how does the number of trials interact with sample size to affect statistical power? Like us, they present an interactive demonstration of their findings https://shiny.york.ac.uk/ powercontours/…”
Section: Related Workmentioning
confidence: 99%