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Power and sample size calculation for stepped-wedge designs with discrete outcomes
BACKGROUND: Stepped-wedge designs (SWD) are increasingly used to evaluate the impact of changes to the process of care within health care systems. However, to generate definitive evidence, a correct sample size calculation is crucial to ensure such studies are properly powered. The seminal work of H...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419932/ https://www.ncbi.nlm.nih.gov/pubmed/34488848 http://dx.doi.org/10.1186/s13063-021-05542-9 |
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author | Xia, Fan Hughes, James P. Voldal, Emily C. Heagerty, Patrick J. |
author_facet | Xia, Fan Hughes, James P. Voldal, Emily C. Heagerty, Patrick J. |
author_sort | Xia, Fan |
collection | PubMed |
description | BACKGROUND: Stepped-wedge designs (SWD) are increasingly used to evaluate the impact of changes to the process of care within health care systems. However, to generate definitive evidence, a correct sample size calculation is crucial to ensure such studies are properly powered. The seminal work of Hussey and Hughes (Contemp Clin Trials 28(2):182–91, 2004) provides an analytical formula for power calculations with normal outcomes using a linear model and simple random effects. However, minimal development and evaluation have been done for power calculation with non-normal outcomes on their natural scale (e.g., logit, log). For example, binary endpoints are common, and logistic regression is the natural multilevel model for such clustered data. METHODS: We propose a power calculation formula for SWD with either normal or non-normal outcomes in the context of generalized linear mixed models by adopting the Laplace approximation detailed in Breslow and Clayton (J Am Stat Assoc 88(421):9–25, 1993) to obtain the covariance matrix of the estimated parameters. RESULTS: We compare the performance of our proposed method with simulation-based sample size calculation and demonstrate its use on a study of patient-delivered partner therapy for STI treatment and a study that assesses the impact of providing additional benchmark prevalence information in a radiologic imaging report. To facilitate adoption of our methods we also provide a function embedded in the R package “swCRTdesign” for sample size and power calculation for multilevel stepped-wedge designs. CONCLUSIONS: Our method requires minimal computational power. Therefore, the proposed procedure facilitates rapid dynamic updates of sample size calculations and can be used to explore a wide range of design options or assumptions. |
format | Online Article Text |
id | pubmed-8419932 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-84199322021-09-09 Power and sample size calculation for stepped-wedge designs with discrete outcomes Xia, Fan Hughes, James P. Voldal, Emily C. Heagerty, Patrick J. Trials Methodology BACKGROUND: Stepped-wedge designs (SWD) are increasingly used to evaluate the impact of changes to the process of care within health care systems. However, to generate definitive evidence, a correct sample size calculation is crucial to ensure such studies are properly powered. The seminal work of Hussey and Hughes (Contemp Clin Trials 28(2):182–91, 2004) provides an analytical formula for power calculations with normal outcomes using a linear model and simple random effects. However, minimal development and evaluation have been done for power calculation with non-normal outcomes on their natural scale (e.g., logit, log). For example, binary endpoints are common, and logistic regression is the natural multilevel model for such clustered data. METHODS: We propose a power calculation formula for SWD with either normal or non-normal outcomes in the context of generalized linear mixed models by adopting the Laplace approximation detailed in Breslow and Clayton (J Am Stat Assoc 88(421):9–25, 1993) to obtain the covariance matrix of the estimated parameters. RESULTS: We compare the performance of our proposed method with simulation-based sample size calculation and demonstrate its use on a study of patient-delivered partner therapy for STI treatment and a study that assesses the impact of providing additional benchmark prevalence information in a radiologic imaging report. To facilitate adoption of our methods we also provide a function embedded in the R package “swCRTdesign” for sample size and power calculation for multilevel stepped-wedge designs. CONCLUSIONS: Our method requires minimal computational power. Therefore, the proposed procedure facilitates rapid dynamic updates of sample size calculations and can be used to explore a wide range of design options or assumptions. BioMed Central 2021-09-06 /pmc/articles/PMC8419932/ /pubmed/34488848 http://dx.doi.org/10.1186/s13063-021-05542-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Methodology Xia, Fan Hughes, James P. Voldal, Emily C. Heagerty, Patrick J. Power and sample size calculation for stepped-wedge designs with discrete outcomes |
title | Power and sample size calculation for stepped-wedge designs with discrete outcomes |
title_full | Power and sample size calculation for stepped-wedge designs with discrete outcomes |
title_fullStr | Power and sample size calculation for stepped-wedge designs with discrete outcomes |
title_full_unstemmed | Power and sample size calculation for stepped-wedge designs with discrete outcomes |
title_short | Power and sample size calculation for stepped-wedge designs with discrete outcomes |
title_sort | power and sample size calculation for stepped-wedge designs with discrete outcomes |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419932/ https://www.ncbi.nlm.nih.gov/pubmed/34488848 http://dx.doi.org/10.1186/s13063-021-05542-9 |
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