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Constrained randomization and statistical inference for multi‐arm parallel cluster randomized controlled trials
Author(s) -
Zhou Yunji,
Turner Elizabeth L.,
Simmons Ryan A.,
Li Fan
Publication year - 2022
Publication title -
statistics in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.996
H-Index - 183
eISSN - 1097-0258
pISSN - 0277-6715
DOI - 10.1002/sim.9333
Subject(s) - randomization , covariate , restricted randomization , inference , pairwise comparison , type i and type ii errors , statistics , statistical power , computer science , statistical inference , econometrics , mathematics , randomized controlled trial , artificial intelligence , medicine , surgery
A practical limitation of cluster randomized controlled trials (cRCTs) is that the number of available clusters may be small, resulting in an increased risk of baseline imbalance under simple randomization. Constrained randomization overcomes this issue by restricting the allocation to a subset of randomization schemes where sufficient overall covariate balance across comparison arms is achieved. However, for multi‐arm cRCTs, several design and analysis issues pertaining to constrained randomization have not been fully investigated. Motivated by an ongoing multi‐arm cRCT, we elaborate the method of constrained randomization and provide a comprehensive evaluation of the statistical properties of model‐based and randomization‐based tests under both simple and constrained randomization designs in multi‐arm cRCTs, with varying combinations of design and analysis‐based covariate adjustment strategies. In particular, as randomization‐based tests have not been extensively studied in multi‐arm cRCTs, we additionally develop most‐powerful randomization tests under the linear mixed model framework for our comparisons. Our results indicate that under constrained randomization, both model‐based and randomization‐based analyses could gain power while preserving nominal type I error rate, given proper analysis‐based adjustment for the baseline covariates. Randomization‐based analyses, however, are more robust against violations of distributional assumptions. The choice of balance metrics and candidate set sizes and their implications on the testing of the pairwise and global hypotheses are also discussed. Finally, we caution against the design and analysis of multi‐arm cRCTs with an extremely small number of clusters, due to insufficient degrees of freedom and the tendency to obtain an overly restricted randomization space.

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