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Estimands in cluster-randomized trials: choosing analyses that answer the right question

BACKGROUND: Cluster-randomized trials (CRTs) involve randomizing groups of individuals (e.g. hospitals, schools or villages) to different interventions. Various approaches exist for analysing CRTs but there has been little discussion around the treatment effects (estimands) targeted by each. METHODS...

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Autores principales: Kahan, Brennan C, Li, Fan, Copas, Andrew J, Harhay, Michael O
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9908044/
https://www.ncbi.nlm.nih.gov/pubmed/35834775
http://dx.doi.org/10.1093/ije/dyac131
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author Kahan, Brennan C
Li, Fan
Copas, Andrew J
Harhay, Michael O
author_facet Kahan, Brennan C
Li, Fan
Copas, Andrew J
Harhay, Michael O
author_sort Kahan, Brennan C
collection PubMed
description BACKGROUND: Cluster-randomized trials (CRTs) involve randomizing groups of individuals (e.g. hospitals, schools or villages) to different interventions. Various approaches exist for analysing CRTs but there has been little discussion around the treatment effects (estimands) targeted by each. METHODS: We describe the different estimands that can be addressed through CRTs and demonstrate how choices between different analytic approaches can impact the interpretation of results by fundamentally changing the question being asked, or, equivalently, the target estimand. RESULTS: CRTs can address either the participant-average treatment effect (the average treatment effect across participants) or the cluster-average treatment effect (the average treatment effect across clusters). These two estimands can differ when participant outcomes or the treatment effect depends on the cluster size (referred to as ‘informative cluster size’), which can occur for reasons such as differences in staffing levels or types of participants between small and large clusters. Furthermore, common estimators, such as mixed-effects models or generalized estimating equations with an exchangeable working correlation structure, can produce biased estimates for both the participant-average and cluster-average treatment effects when cluster size is informative. We describe alternative estimators (independence estimating equations and cluster-level analyses) that are unbiased for CRTs even when informative cluster size is present. CONCLUSION: We conclude that careful specification of the estimand at the outset can ensure that the study question being addressed is clear and relevant, and, in turn, that the selected estimator provides an unbiased estimate of the desired quantity.
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spelling pubmed-99080442023-02-09 Estimands in cluster-randomized trials: choosing analyses that answer the right question Kahan, Brennan C Li, Fan Copas, Andrew J Harhay, Michael O Int J Epidemiol More on RCTs BACKGROUND: Cluster-randomized trials (CRTs) involve randomizing groups of individuals (e.g. hospitals, schools or villages) to different interventions. Various approaches exist for analysing CRTs but there has been little discussion around the treatment effects (estimands) targeted by each. METHODS: We describe the different estimands that can be addressed through CRTs and demonstrate how choices between different analytic approaches can impact the interpretation of results by fundamentally changing the question being asked, or, equivalently, the target estimand. RESULTS: CRTs can address either the participant-average treatment effect (the average treatment effect across participants) or the cluster-average treatment effect (the average treatment effect across clusters). These two estimands can differ when participant outcomes or the treatment effect depends on the cluster size (referred to as ‘informative cluster size’), which can occur for reasons such as differences in staffing levels or types of participants between small and large clusters. Furthermore, common estimators, such as mixed-effects models or generalized estimating equations with an exchangeable working correlation structure, can produce biased estimates for both the participant-average and cluster-average treatment effects when cluster size is informative. We describe alternative estimators (independence estimating equations and cluster-level analyses) that are unbiased for CRTs even when informative cluster size is present. CONCLUSION: We conclude that careful specification of the estimand at the outset can ensure that the study question being addressed is clear and relevant, and, in turn, that the selected estimator provides an unbiased estimate of the desired quantity. Oxford University Press 2022-07-14 /pmc/articles/PMC9908044/ /pubmed/35834775 http://dx.doi.org/10.1093/ije/dyac131 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the International Epidemiological Association. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle More on RCTs
Kahan, Brennan C
Li, Fan
Copas, Andrew J
Harhay, Michael O
Estimands in cluster-randomized trials: choosing analyses that answer the right question
title Estimands in cluster-randomized trials: choosing analyses that answer the right question
title_full Estimands in cluster-randomized trials: choosing analyses that answer the right question
title_fullStr Estimands in cluster-randomized trials: choosing analyses that answer the right question
title_full_unstemmed Estimands in cluster-randomized trials: choosing analyses that answer the right question
title_short Estimands in cluster-randomized trials: choosing analyses that answer the right question
title_sort estimands in cluster-randomized trials: choosing analyses that answer the right question
topic More on RCTs
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9908044/
https://www.ncbi.nlm.nih.gov/pubmed/35834775
http://dx.doi.org/10.1093/ije/dyac131
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