Evidence map›Paper›PMID 35418034›Full record

ArticleBMC medical research methodology2022

Evaluating the performance of Bayesian and restricted maximum likelihood estimation for stepped wedge cluster randomized trials with a small number of clusters.

Kelsey L Grantham, Jessica Kasza, Stephane Heritier, John B Carlin, Andrew B Forbes

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Article in BMC medical research methodology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

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10citing papers in PubMed, 1 pooled it
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Kelsey L GranthamSchool of Public Health and Preventive Medicine, Monash University, Melbourne, Australia.
Jessica KaszaSchool of Public Health and Preventive Medicine, Monash University, Melbourne, Australia.
Stephane HeritierSchool of Public Health and Preventive Medicine, Monash University, Melbourne, Australia.
John B CarlinClinical Epidemiology and Biostatistics Unit, Murdoch Children's Research Institute, Parkville, Australia.
Andrew B ForbesSchool of Public Health and Preventive Medicine, Monash University, Melbourne, Australia. andrew.forbes@monash.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStepped wedge trials are an appealing and potentially powerful cluster randomized trial design. However, they are frequently implemented with a small number of clusters. Standard analysis methods for these trials such as a linear mixed model with estimation via maximum likelihood or restricted maximum likelihood (REML) rely on asymptotic properties and have been shown to yield inflated type I error when applied to studies with a small number of clusters. Small-sample methods such as the Kenward-Roger approximation in combination with REML can potentially improve estimation of the fixed effects such as the treatment effect. A Bayesian approach may also be promising for such multilevel models but has not yet seen much application in cluster randomized trials.

methodsWe conducted a simulation study comparing the performance of REML with and without a Kenward-Roger approximation to a Bayesian approach using weakly informative prior distributions on the intracluster correlation parameters. We considered a continuous outcome and a range of stepped wedge trial configurations with between 4 and 40 clusters. To assess method performance we calculated bias and mean squared error for the treatment effect and correlation parameters and the coverage of 95% confidence/credible intervals and relative percent error in model-based standard error for the treatment effect.

resultsBoth REML with a Kenward-Roger standard error and degrees of freedom correction and the Bayesian method performed similarly well for the estimation of the treatment effect, while intracluster correlation parameter estimates obtained via the Bayesian method were less variable than REML estimates with different relative levels of bias.

conclusionsThe use of REML with a Kenward-Roger approximation may be sufficient for the analysis of stepped wedge cluster randomized trials with a small number of clusters. However, a Bayesian approach with weakly informative prior distributions on the intracluster correlation parameters offers a viable alternative, particularly when there is interest in the probability-based inferences permitted within this paradigm.

Indexed as

Research DesignBayes TheoremCluster AnalysisComputer SimulationHumansLikelihood FunctionsRandomized Controlled Trials as TopicSample SizeBayesian inferenceCluster randomized trialIntracluster correlationRestricted maximum likelihoodSimulation studyStepped wedge

Identifiers

PMID35418034
PMCPMC9009029

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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.