Power analysis for cluster randomized trials with continuous co-primary endpoints
Siyun Yang, Mirjam Moerbeek, Monica Taljaard, Fan Li

TL;DR
This paper develops a statistical method for power analysis in cluster randomized trials with multiple continuous co-primary endpoints, accounting for complex correlation structures, to improve sample size determination.
Contribution
It introduces a multivariate linear mixed model framework for continuous endpoints, deriving the joint distribution of treatment effects for power analysis in CRTs with multiple co-primary endpoints.
Findings
Predicted power aligns well with empirical power in simulations.
Method accommodates unequal cluster sizes through approximation.
Application to real CRT demonstrates practical utility.
Abstract
Pragmatic trials evaluating health care interventions often adopt cluster randomization due to scientific or logistical considerations. Previous reviews have shown that co-primary endpoints are common in pragmatic trials but infrequently recognized in sample size or power calculations. While methods for power analysis based on () binary co-primary endpoints are available for CRTs, to our knowledge, methods for continuous co-primary endpoints are not yet available. Assuming a multivariate linear mixed model that accounts for multiple types of intraclass correlation coefficients (endpoint-specific ICCs, intra-subject ICCs and inter-subject between-endpoint ICCs) among the observations in each cluster, we derive the closed-form joint distribution of treatment effect estimators to facilitate sample size and power determination with different types of null hypotheses under…
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Taxonomy
TopicsAdvanced Causal Inference Techniques · Statistical Methods and Bayesian Inference · Statistical Methods in Clinical Trials
