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Power Contours: Optimising Sample Size and Precision in Experimental Psychology and Human Neuroscience
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 as...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Psychological Association
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8329985/ https://www.ncbi.nlm.nih.gov/pubmed/32673043 http://dx.doi.org/10.1037/met0000337 |
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author | Baker, Daniel H. Vilidaite, Greta Lygo, Freya A. Smith, Anika K. Flack, Tessa R. Gouws, André D. Andrews, Timothy J. |
author_facet | Baker, Daniel H. Vilidaite, Greta Lygo, Freya A. Smith, Anika K. Flack, Tessa R. Gouws, André D. Andrews, Timothy J. |
author_sort | Baker, Daniel H. |
collection | PubMed |
description | 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 which the number of trials is particularly important, that is, when the within-participant variance is large relative to the between-participants variance. We then derive power contour plots using existing data sets for 8 experimental paradigms and methodologies (including reaction times, sensory thresholds, fMRI, MEG, and EEG), and provide example code to calculate estimates of the within- and between-participants variance for each method. In all cases, the within-participant variance was larger than the between-participants variance, meaning that the number of trials has a meaningful influence on statistical power in commonly used paradigms. An online tool is provided (https://shiny.york.ac.uk/powercontours/) for generating power contours, from which the optimal combination of trials and participants can be calculated when designing future studies. |
format | Online Article Text |
id | pubmed-8329985 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Psychological Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-83299852021-08-11 Power Contours: Optimising Sample Size and Precision in Experimental Psychology and Human Neuroscience Baker, Daniel H. Vilidaite, Greta Lygo, Freya A. Smith, Anika K. Flack, Tessa R. Gouws, André D. Andrews, Timothy J. Psychol Methods Articles 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 which the number of trials is particularly important, that is, when the within-participant variance is large relative to the between-participants variance. We then derive power contour plots using existing data sets for 8 experimental paradigms and methodologies (including reaction times, sensory thresholds, fMRI, MEG, and EEG), and provide example code to calculate estimates of the within- and between-participants variance for each method. In all cases, the within-participant variance was larger than the between-participants variance, meaning that the number of trials has a meaningful influence on statistical power in commonly used paradigms. An online tool is provided (https://shiny.york.ac.uk/powercontours/) for generating power contours, from which the optimal combination of trials and participants can be calculated when designing future studies. American Psychological Association 2020-07-16 2021-06 /pmc/articles/PMC8329985/ /pubmed/32673043 http://dx.doi.org/10.1037/met0000337 Text en © 2020 The Author(s) https://creativecommons.org/licenses/by/3.0/This article has been published under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Copyright for this article is retained by the author(s). Author(s) grant(s) the American Psychological Association the exclusive right to publish the article and identify itself as the original publisher. |
spellingShingle | Articles Baker, Daniel H. Vilidaite, Greta Lygo, Freya A. Smith, Anika K. Flack, Tessa R. Gouws, André D. Andrews, Timothy J. Power Contours: Optimising Sample Size and Precision in Experimental Psychology and Human Neuroscience |
title | Power Contours: Optimising Sample Size and Precision in Experimental Psychology and Human Neuroscience |
title_full | Power Contours: Optimising Sample Size and Precision in Experimental Psychology and Human Neuroscience |
title_fullStr | Power Contours: Optimising Sample Size and Precision in Experimental Psychology and Human Neuroscience |
title_full_unstemmed | Power Contours: Optimising Sample Size and Precision in Experimental Psychology and Human Neuroscience |
title_short | Power Contours: Optimising Sample Size and Precision in Experimental Psychology and Human Neuroscience |
title_sort | power contours: optimising sample size and precision in experimental psychology and human neuroscience |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8329985/ https://www.ncbi.nlm.nih.gov/pubmed/32673043 http://dx.doi.org/10.1037/met0000337 |
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