In stepped cluster designs the intervention is introduced into some (or all) clusters at different times and persists until the end of the study. Instances include traditional parallel cluster designs and the more recent stepped-wedge designs. We consider the precision offered by such designs under mixed-effects models with fixed time and random subject and cluster effects (including interactions with time), and explore the optimal choice of uptake times. The results apply both to cross-sectional studies where new subjects are observed at each time-point, and longitudinal studies with repeat observations on the same subjects. The efficiency of the design is expressed in terms of a 'cluster-mean correlation' which carries information about the dependency-structure of the data, and two design coefficients which reflect the pattern of uptake-times. In cross-sectional studies the cluster-mean correlation combines information about the cluster-size and the intra-cluster correlation coefficient. A formula is given for the 'design effect' in both cross-sectional and longitudinal studies. An algorithm for optimising the choice of uptake times is described and specific results obtained for the best balanced stepped designs. In large studies we show that the best design is a hybrid mixture of parallel and stepped-wedge components, with the proportion of stepped wedge clusters equal to the cluster-mean correlation. The impact of prior uncertainty in the cluster-mean correlation is considered by simulation. Some specific hybrid designs are proposed for consideration when the cluster-mean correlation cannot be reliably estimated, using a minimax principle to ensure acceptable performance across the whole range of unknown values. (C) 2016 The Authors. Statistics in Medicine published by John Wiley & Sons Ltd.
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UNT Hlth Sci Ctr, Dept Biostat, Ft Worth, TX 76107 USA
UNT Hlth Sci Ctr, Osteopath Res Ctr, Ft Worth, TX USAUNT Hlth Sci Ctr, Dept Biostat, Ft Worth, TX 76107 USA
Aryal, Subhash
Bhaumik, Dulal K.
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Univ Illinois, Dept Biostat, Chicago, IL 60680 USA
Univ Illinois, Dept Psychiat, Chicago, IL 60680 USAUNT Hlth Sci Ctr, Dept Biostat, Ft Worth, TX 76107 USA
Bhaumik, Dulal K.
Mathew, Thomas
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Univ Maryland, Dept Stat, Baltimore, MD 21201 USAUNT Hlth Sci Ctr, Dept Biostat, Ft Worth, TX 76107 USA
Mathew, Thomas
Gibbons, Robert D.
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Univ Chicago, Ctr Hlth Stat, Chicago, IL 60637 USAUNT Hlth Sci Ctr, Dept Biostat, Ft Worth, TX 76107 USA
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Int Drug Dev Inst IDDI SA, Louvain, BelgiumCatholic Univ Louvain, Inst Stat Biostat & Sci Actuarielles ISBA, B-1348 Louvain, Belgium
Doffagne, E.
Timmermans, C.
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Int Drug Dev Inst IDDI SA, Louvain, BelgiumCatholic Univ Louvain, Inst Stat Biostat & Sci Actuarielles ISBA, B-1348 Louvain, Belgium
Timmermans, C.
Burzykowski, T.
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Int Drug Dev Inst IDDI SA, Louvain, Belgium
Hasselt Univ, Interuniv Inst Biostat & Stat Bioinformat I BioSt, Diepenbeek, BelgiumCatholic Univ Louvain, Inst Stat Biostat & Sci Actuarielles ISBA, B-1348 Louvain, Belgium
Burzykowski, T.
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Legrand, C.
Buyse, M.
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Hasselt Univ, Interuniv Inst Biostat & Stat Bioinformat I BioSt, Diepenbeek, Belgium
Int Drug Dev Inst IDDI Inc, San Francisco, CA USACatholic Univ Louvain, Inst Stat Biostat & Sci Actuarielles ISBA, B-1348 Louvain, Belgium