ArticleBiometrical journal. Biometrische Zeitschrift2018
Blinded and unblinded sample size reestimation procedures for stepped-wedge cluster randomized trials.
Article in Biometrical journal. Biometrische Zeitschrift, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Power analysis for concurrent balanced or imbalanced multiple-intervention stepped wedge design: a simulation-based approach.BMC medical research methodology · 2025Article
- Response adaptive intervention allocation in stepped-wedge cluster randomized trials.Statistics in medicine · 2022Article
- Interim data monitoring in cluster randomised trials: Practical issues and a case study.Clinical trials (London, England) · 2021Article
- Sample size and power considerations for cluster randomized trials with count outcomes subject to right truncation.Biometrical journal. Biometrische Zeitschrift · 2021Article
- Blinded and unblinded sample size reestimation procedures for stepped-wedge cluster randomized trials.Biometrical journal. Biometrische Zeitschrift · 2018Article
Corrections and comments
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Authors and funding
3 authors.
Funding
Abstract
The ability to accurately estimate the sample size required by a stepped-wedge (SW) cluster randomized trial (CRT) routinely depends upon the specification of several nuisance parameters. If these parameters are misspecified, the trial could be overpowered, leading to increased cost, or underpowered, enhancing the likelihood of a false negative. We address this issue here for cross-sectional SW-CRTs, analyzed with a particular linear-mixed model, by proposing methods for blinded and unblinded sample size reestimation (SSRE). First, blinded estimators for the variance parameters of a SW-CRT analyzed using the Hussey and Hughes model are derived. Following this, procedures for blinded and unblinded SSRE after any time period in a SW-CRT are detailed. The performance of these procedures is then examined and contrasted using two example trial design scenarios. We find that if the two key variance parameters were underspecified by 50%, the SSRE procedures were able to increase power over the conventional SW-CRT design by up to 41%, resulting in an empirical power above the desired level. Thus, though there are practical issues to consider, the performance of the procedures means researchers should consider incorporating SSRE in to future SW-CRTs.
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Registered trials
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