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Variations in stepped-wedge cluster randomized trial design: Insights from the Patient-Centered Care Transitions in Heart Failure trial - 05/02/20

Doi : 10.1016/j.ahj.2019.08.017 
Rudy R. Unni, MD a, Shun Fu Lee, PhD b, Lehana Thabane, PhD c, Stuart Connolly, MSc, MD b, Harriette GC Van Spall, MD, MPH b, c, d,
a Department of Medicine, University of Ottawa, Ottawa, Ontario, Canada 
b Population Health Research Institute, McMaster University, Hamilton, Ontario, Canada 
c Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, Ontario, Canada 
d Department of Medicine, McMaster University, Hamilton, Ontario, Canada 

Reprint requests: Harriette GC Van Spall, M.D, MPH, FRCPC, Population Health Research Institute, 20 Copeland Ave David Braley Research Institute Bldg, Suite C3-117, Hamilton, ON L8L 0A3.Population Health Research Institute20 Copeland Ave David Braley Research Institute Bldg, Suite C3-117HamiltonONL8L 0A3

Abstract

The stepped-wedge (SW) cluster randomized controlled trial, in which clusters cross over in a randomized sequence from control to intervention, is ideal for the implementation and testing of complex health service interventions. In certain cases however, implementation of the intervention may pose logistical challenges, and variations in SW design may be required.

We examine the logistical and statistical implications of variations in SW design using the optimization of the Patient-Centered Care Transitions in Heart Failure trial for illustration. We review the following complete SW design variations: a typical SW design; an SW design with multiple clusters crossing over per period to achieve balanced cluster sizes at each step; hierarchical randomization to account for higher-level clustering effects; nested substudies to measure outcomes requiring a smaller sample size than the primary outcomes; and hybrid SW design, which combines parallel cluster with SW design to improve efficiency. We also reviewed 3 incomplete SW design variations in which data are collected in some but not all steps to ease measurement burden. These include designs with a learning period that improve fidelity to the intervention, designs with reduced measurements to minimize collection burden, and designs with early and late blocks to accommodate cluster readiness.

Variations in SW design offer pragmatic solutions to logistical challenges but have implications to statistical power. Advantages and disadvantages of each variation should be considered before finalizing the design of an SW randomized controlled trial.

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 Funding: This study is funded by Canadian Institutes of Health Research and Ontario's Ministry of Health and Long Term Care Health System Research Fund. Dr Van Spall receives research salary support from Ontario's Ministry of Health and Hamilton Health Sciences Career Award.
 Disclosures: none.
The senior author is responsible for the design and conduct of the PACT-HF study. The authors are responsible for the present analyses, drafting and editing of the paper, and its final contents.


© 2019  Elsevier Inc. Tutti i diritti riservati.
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Vol 220

P. 116-126 - Febbraio 2020 Ritorno al numero
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