scholarly journals Stepped wedge designs could reduce the required sample size in cluster randomized trials

2013 ◽  
Vol 66 (7) ◽  
pp. 752-758 ◽  
Author(s):  
Willem Woertman ◽  
Esther de Hoop ◽  
Mirjam Moerbeek ◽  
Sytse U. Zuidema ◽  
Debby L. Gerritsen ◽  
...  
2019 ◽  
Vol 107 ◽  
pp. 89-100 ◽  
Author(s):  
Felizitas A. Eichner ◽  
Rolf H.H. Groenwold ◽  
Diederick E. Grobbee ◽  
Katrien Oude Rengerink

2018 ◽  
Vol 60 (5) ◽  
pp. 903-916 ◽  
Author(s):  
Michael J. Grayling ◽  
Adrian P. Mander ◽  
James M. S. Wason

2021 ◽  
Author(s):  
Zibo Tian ◽  
John Preisser ◽  
Denise Esserman ◽  
Elizabeth Turner ◽  
Paul Rathouz ◽  
...  

The stepped wedge design is a type of unidirectional crossover design where cluster units switch from control to intervention condition at different pre-specified time points. While a convention in study planning is to assume the cluster-period sizes are identical, stepped wedge cluster randomized trials (SW-CRTs) involving repeated cross-sectional designs frequently have unequal cluster-period sizes, which can impact the efficiency of the treatment effect estimator. In this article, we provide a comprehensive investigation of the efficiency impact of unequal cluster sizes for generalized estimating equation analyses of SW-CRTs, with a focus on binary outcomes as in the Washington State Expedited Partner Therapy trial. Several major distinctions between our work and existing work include: (i) we consider multilevel correlation structures in marginal models with binary outcomes; (ii) we study the implications of both the between-cluster and within-cluster imbalances in sizes; and (iii) we provide a comparison between the independence working correlation versus the true working correlation and detail the consequences of ignoring correlation estimation in SW-CRTs with unequal cluster sizes. We conclude that the working independence assumption can lead to substantial efficiency loss and a large sample size regardless of cluster-period size variability in SW-CRTs, and recommend accounting for correlations in the analysis. To improve study planning, we additionally provide a computationally efficient search algorithm to estimate the sample size in SW-CRTs accounting for unequal cluster-period sizes, and conclude by illustrating the proposed approach in the context of the Washington State study.


2010 ◽  
Vol 8 (1) ◽  
pp. 27-36 ◽  
Author(s):  
Zhiying You ◽  
O Dale Williams ◽  
Inmaculada Aban ◽  
Edmond Kato Kabagambe ◽  
Hemant K Tiwari ◽  
...  

2021 ◽  
pp. 096228022199041
Author(s):  
Fan Li ◽  
Guangyu Tong

The modified Poisson regression coupled with a robust sandwich variance has become a viable alternative to log-binomial regression for estimating the marginal relative risk in cluster randomized trials. However, a corresponding sample size formula for relative risk regression via the modified Poisson model is currently not available for cluster randomized trials. Through analytical derivations, we show that there is no loss of asymptotic efficiency for estimating the marginal relative risk via the modified Poisson regression relative to the log-binomial regression. This finding holds both under the independence working correlation and under the exchangeable working correlation provided a simple modification is used to obtain the consistent intraclass correlation coefficient estimate. Therefore, the sample size formulas developed for log-binomial regression naturally apply to the modified Poisson regression in cluster randomized trials. We further extend the sample size formulas to accommodate variable cluster sizes. An extensive Monte Carlo simulation study is carried out to validate the proposed formulas. We find that the proposed formulas have satisfactory performance across a range of cluster size variability, as long as suitable finite-sample corrections are applied to the sandwich variance estimator and the number of clusters is at least 10. Our findings also suggest that the sample size estimate under the exchangeable working correlation is more robust to cluster size variability, and recommend the use of an exchangeable working correlation over an independence working correlation for both design and analysis. The proposed sample size formulas are illustrated using the Stop Colorectal Cancer (STOP CRC) trial.


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