Evidence map›Paper›PMID 39844041›Full record

ArticleBMC medical research methodology2025

Analysis methods for covariate-constrained cluster randomized trials with time-to-event outcomes.

Amy M Crisp, M Elizabeth Halloran, Matt D T Hitchings, Ira M Longini, Natalie E Dean

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Article in BMC medical research methodology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Amy M CrispDepartment of Biostatistics, University of Florida, Gainesville, Florida, USA. amy.crisp@jax.ufl.edu.
M Elizabeth HalloranDepartment of Biostatistics, University of Washington, Seattle, Washington, USA.
Matt D T HitchingsDepartment of Biostatistics, University of Florida, Gainesville, Florida, USA.
Ira M LonginiDepartment of Biostatistics, University of Florida, Gainesville, Florida, USA.
Natalie E DeanDepartment of Biostatistics and Bioinformatics, Emory University, Atlanta, Georgia, USA.

Funding

Quanitifying the Epidemiological Impact of Targeted Indoor Residual Spraying on Aedes-borne DiseasesU01AI148069 · NIAID · EMORY UNIVERSITY · PI VAZQUEZ PROKOPEC, GONZALO MARTIN · 2020 to 2024
$6.4M
National Institute of Allergy and Infectious Diseases U01-AI148069NIAID NIH HHS U01 AI148069NIH HHS U01-AI148069
6 · The paper itself

Abstract

backgroundCluster randomized trials, which often enroll a small number of clusters, can benefit from constrained randomization, selecting a final randomization scheme from a set of known, balanced randomizations. Previous literature has addressed the suitability of adjusting the analysis for the covariates that were balanced in the design phase when the outcome is continuous or binary. Here we extended this work to time-to-event outcomes by comparing two model-based tests and a newly derived permutation test. A current cluster randomized trial of vector control for the prevention of mosquito-borne disease in children in Mexico is used as a motivating example.

methodsWe assessed type I error rates and power between simple randomization and constrained randomization using both prognostic and non-prognostic covariates via a simulation study. We compared the performance of a semi-parametric Cox proportional hazards model with robust variance, a mixed effects Cox model, and a permutation test utilizing deviance residuals.

resultsThe permutation test generally maintained nominal type I error-with the exception of the unadjusted analysis for constrained randomization-and also provided power comparable to the two Cox model-based tests. The model-based tests had inflated type I error when there were very few clusters per trial arm. All three methods performed well when there were 25 clusters per trial arm, as in the case of the motivating example.

conclusionFor time-to-event outcomes, covariate-constrained randomization was shown to improve power relative to simple randomization. The permutation test developed here was more robust to inflation of type I error compared to model-based tests. Gaining power by adjusting for covariates in the analysis phase was largely dependent on the number of clusters per trial arm.

Indexed as

Randomized Controlled Trials as TopicChildCluster AnalysisComputer SimulationHumansMexicoProportional Hazards ModelsClinical trial designCluster-randomizedConstrained randomizationPermutation testTime-to-event

Identifiers

PMID39844041
PMCPMC11753003

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.