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Performance of methods for analyzing continuous data from stratified cluster randomized trials – A simulation study
BACKGROUND: The adoption of cluster randomized trials (CRTs) with the stratified design is currently gaining widespread interest. In the stratified design, clusters are first grouped into two or more strata and then randomized into treatment groups within each stratum. In this study, we evaluated th...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10313865/ https://www.ncbi.nlm.nih.gov/pubmed/37397432 http://dx.doi.org/10.1016/j.conctc.2023.101115 |
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author | Borhan, Sayem Ma, Jinhui Papaioannou, Alexandra Adachi, Jonathan Thabane, Lehana |
author_facet | Borhan, Sayem Ma, Jinhui Papaioannou, Alexandra Adachi, Jonathan Thabane, Lehana |
author_sort | Borhan, Sayem |
collection | PubMed |
description | BACKGROUND: The adoption of cluster randomized trials (CRTs) with the stratified design is currently gaining widespread interest. In the stratified design, clusters are first grouped into two or more strata and then randomized into treatment groups within each stratum. In this study, we evaluated the performance of several commonly used methods for analyzing continuous data from stratified CRTs. METHODS: This is a simulation study where we compared four methods: mixed-effects, generalized estimating equation (GEE), cluster-level (CL) linear regression and meta-regression methods to analyze the continuous data from stratified CRTs using a simulation study with varying numbers of clusters, cluster sizes, intra-cluster correlation coefficients (ICCs) and effect sizes. This study was based on a stratified CRT with one stratification variable with two strata. The performance of the methods was evaluated in terms of the type I error rate, empirical power, root mean square error (RMSE), and width and coverage of the 95% confidence interval (CI). RESULTS: GEE and meta-regression methods had high type I error rates, higher than 10%, for the small number of clusters. All methods had similar accuracy, measured through RMSE, except meta-regression. Similarly, all methods but meta-regression had similar widths of 95% CIs for the small number of clusters. For the same sample size, the empirical power for all methods decreased as the value of the ICC increased. CONCLUSION: In this study, we evaluated the performance of several methods for analyzing continuous data from stratified CRTs. Meta-regression was the least efficient method compared to other methods. |
format | Online Article Text |
id | pubmed-10313865 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-103138652023-07-02 Performance of methods for analyzing continuous data from stratified cluster randomized trials – A simulation study Borhan, Sayem Ma, Jinhui Papaioannou, Alexandra Adachi, Jonathan Thabane, Lehana Contemp Clin Trials Commun Article BACKGROUND: The adoption of cluster randomized trials (CRTs) with the stratified design is currently gaining widespread interest. In the stratified design, clusters are first grouped into two or more strata and then randomized into treatment groups within each stratum. In this study, we evaluated the performance of several commonly used methods for analyzing continuous data from stratified CRTs. METHODS: This is a simulation study where we compared four methods: mixed-effects, generalized estimating equation (GEE), cluster-level (CL) linear regression and meta-regression methods to analyze the continuous data from stratified CRTs using a simulation study with varying numbers of clusters, cluster sizes, intra-cluster correlation coefficients (ICCs) and effect sizes. This study was based on a stratified CRT with one stratification variable with two strata. The performance of the methods was evaluated in terms of the type I error rate, empirical power, root mean square error (RMSE), and width and coverage of the 95% confidence interval (CI). RESULTS: GEE and meta-regression methods had high type I error rates, higher than 10%, for the small number of clusters. All methods had similar accuracy, measured through RMSE, except meta-regression. Similarly, all methods but meta-regression had similar widths of 95% CIs for the small number of clusters. For the same sample size, the empirical power for all methods decreased as the value of the ICC increased. CONCLUSION: In this study, we evaluated the performance of several methods for analyzing continuous data from stratified CRTs. Meta-regression was the least efficient method compared to other methods. Elsevier 2023-03-14 /pmc/articles/PMC10313865/ /pubmed/37397432 http://dx.doi.org/10.1016/j.conctc.2023.101115 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Borhan, Sayem Ma, Jinhui Papaioannou, Alexandra Adachi, Jonathan Thabane, Lehana Performance of methods for analyzing continuous data from stratified cluster randomized trials – A simulation study |
title | Performance of methods for analyzing continuous data from stratified cluster randomized trials – A simulation study |
title_full | Performance of methods for analyzing continuous data from stratified cluster randomized trials – A simulation study |
title_fullStr | Performance of methods for analyzing continuous data from stratified cluster randomized trials – A simulation study |
title_full_unstemmed | Performance of methods for analyzing continuous data from stratified cluster randomized trials – A simulation study |
title_short | Performance of methods for analyzing continuous data from stratified cluster randomized trials – A simulation study |
title_sort | performance of methods for analyzing continuous data from stratified cluster randomized trials – a simulation study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10313865/ https://www.ncbi.nlm.nih.gov/pubmed/37397432 http://dx.doi.org/10.1016/j.conctc.2023.101115 |
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