Longitudinal and repeated cross-sectional cluster-randomization designs using mixed effects regression for binary outcomes: bias and coverage of frequentist and Bayesian methods
As medical applications for cluster randomization designs become more common, investigators look for guidance on optimal methods for estimating the effect of group‐based interventions over time. This study examines two distinct cluster randomization designs: (1) the repeated cross‐sectional design i...
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description | As medical applications for cluster randomization designs become more common, investigators look for guidance on optimal methods for estimating the effect of group‐based interventions over time. This study examines two distinct cluster randomization designs: (1) the repeated cross‐sectional design in which centres are followed over time but patients change, and (2) the longitudinal design in which individual patients are followed over time within treatment clusters. Simulations of each study design stipulated a multiplicative treatment effect (on the log odds scale), between 5 and 15 clusters in each of two treatment arms, and followed over two time periods. Estimation options included linear mixed effects models using restricted maximum likelihood (REML), generalized estimating equations (GEE), mixed effects logistic regression using both penalized quasi likelihood (PQL) and numerical integration, and Bayesian Monte Carlo analysis. For the repeated cross‐sectional designs, most methods performed well in terms of bias and coverage when clusters were numerous (30) and variability across clusters of baseline risk and treatment effect was modest. With few clusters (two groups of five) and higher variability, only the Bayesian methods maintained coverage. In the longitudinal designs, the common methods of REML, GEE, or PQL performed poorly when compared to numerical integration, while Bayesian methods demonstrated less bias and better coverage for estimates of both log odds ratios and risk differences. The performance of common statistical tools for the analysis of cluster randomization designs depends heavily on the precise design, the number of clusters, and the variability of baseline outcomes and treatment effects across centres. Copyright © 2005 John Wiley & Sons, Ltd. |
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Russell ; Berlin, Jesse A. ; Have, Thomas R. Ten</creator><creatorcontrib>Localio, A. Russell ; Berlin, Jesse A. ; Have, Thomas R. Ten</creatorcontrib><description>As medical applications for cluster randomization designs become more common, investigators look for guidance on optimal methods for estimating the effect of group‐based interventions over time. This study examines two distinct cluster randomization designs: (1) the repeated cross‐sectional design in which centres are followed over time but patients change, and (2) the longitudinal design in which individual patients are followed over time within treatment clusters. Simulations of each study design stipulated a multiplicative treatment effect (on the log odds scale), between 5 and 15 clusters in each of two treatment arms, and followed over two time periods. Estimation options included linear mixed effects models using restricted maximum likelihood (REML), generalized estimating equations (GEE), mixed effects logistic regression using both penalized quasi likelihood (PQL) and numerical integration, and Bayesian Monte Carlo analysis. For the repeated cross‐sectional designs, most methods performed well in terms of bias and coverage when clusters were numerous (30) and variability across clusters of baseline risk and treatment effect was modest. With few clusters (two groups of five) and higher variability, only the Bayesian methods maintained coverage. In the longitudinal designs, the common methods of REML, GEE, or PQL performed poorly when compared to numerical integration, while Bayesian methods demonstrated less bias and better coverage for estimates of both log odds ratios and risk differences. The performance of common statistical tools for the analysis of cluster randomization designs depends heavily on the precise design, the number of clusters, and the variability of baseline outcomes and treatment effects across centres. 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Russell</creatorcontrib><creatorcontrib>Berlin, Jesse A.</creatorcontrib><creatorcontrib>Have, Thomas R. Ten</creatorcontrib><title>Longitudinal and repeated cross-sectional cluster-randomization designs using mixed effects regression for binary outcomes: bias and coverage of frequentist and Bayesian methods</title><title>Statistics in medicine</title><addtitle>Statist. Med</addtitle><description>As medical applications for cluster randomization designs become more common, investigators look for guidance on optimal methods for estimating the effect of group‐based interventions over time. This study examines two distinct cluster randomization designs: (1) the repeated cross‐sectional design in which centres are followed over time but patients change, and (2) the longitudinal design in which individual patients are followed over time within treatment clusters. Simulations of each study design stipulated a multiplicative treatment effect (on the log odds scale), between 5 and 15 clusters in each of two treatment arms, and followed over two time periods. Estimation options included linear mixed effects models using restricted maximum likelihood (REML), generalized estimating equations (GEE), mixed effects logistic regression using both penalized quasi likelihood (PQL) and numerical integration, and Bayesian Monte Carlo analysis. For the repeated cross‐sectional designs, most methods performed well in terms of bias and coverage when clusters were numerous (30) and variability across clusters of baseline risk and treatment effect was modest. With few clusters (two groups of five) and higher variability, only the Bayesian methods maintained coverage. In the longitudinal designs, the common methods of REML, GEE, or PQL performed poorly when compared to numerical integration, while Bayesian methods demonstrated less bias and better coverage for estimates of both log odds ratios and risk differences. The performance of common statistical tools for the analysis of cluster randomization designs depends heavily on the precise design, the number of clusters, and the variability of baseline outcomes and treatment effects across centres. 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With few clusters (two groups of five) and higher variability, only the Bayesian methods maintained coverage. In the longitudinal designs, the common methods of REML, GEE, or PQL performed poorly when compared to numerical integration, while Bayesian methods demonstrated less bias and better coverage for estimates of both log odds ratios and risk differences. The performance of common statistical tools for the analysis of cluster randomization designs depends heavily on the precise design, the number of clusters, and the variability of baseline outcomes and treatment effects across centres. Copyright © 2005 John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>16345043</pmid><doi>10.1002/sim.2428</doi><tpages>17</tpages></addata></record> |
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subjects | Bayes Theorem Bayesian analysis Bayesian and frequentist methods Bias Biometry Clinical outcomes Clinical trials Cluster Analysis cluster randomization designs Computer Simulation Cross-Sectional Studies Databases, Factual Drug therapy generalized linear mixed models Humans Likelihood Functions Logistic Models Longitudinal Studies Monte Carlo Method Monte Carlo simulation Random Allocation Randomized Controlled Trials as Topic - methods Randomized Controlled Trials as Topic - statistics & numerical data Regression Analysis |
title | Longitudinal and repeated cross-sectional cluster-randomization designs using mixed effects regression for binary outcomes: bias and coverage of frequentist and Bayesian methods |
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