AI Article Synopsis

  • - The article reviews different designs for cluster randomised trials, focusing on the timing of control and intervention states, observation frequency, and the complexity of identifying efficient designs due to correlated observations.
  • - It presents three main classes of methods for optimizing trial designs: exact formulae for treatment effect variance, generalised weight estimation for experimental units, and combinatorial optimisation algorithms to choose the best subset of units.
  • - The authors also discuss techniques for adjusting experimental weights, applying concepts to non-Gaussian models, and demonstrate their findings through various cluster trial examples, including optimal allocation and observation strategies for different covariance structures.

Article Abstract

There are multiple possible cluster randomised trial designs that vary in when the clusters cross between control and intervention states, when observations are made within clusters, and how many observations are made at each time point. Identifying the most efficient study design is complex though, owing to the correlation between observations within clusters and over time. In this article, we present a review of statistical and computational methods for identifying optimal cluster randomised trial designs. We also adapt methods from the experimental design literature for experimental designs with correlated observations to the cluster trial context. We identify three broad classes of methods: using exact formulae for the treatment effect estimator variance for specific models to derive algorithms or weights for cluster sequences; generalised methods for estimating weights for experimental units; and, combinatorial optimisation algorithms to select an optimal subset of experimental units. We also discuss methods for rounding experimental weights, extensions to non-Gaussian models, and robust optimality. We present results from multiple cluster trial examples that compare the different methods, including determination of the optimal allocation of clusters across a set of cluster sequences and selecting the optimal number of single observations to make in each cluster-period for both Gaussian and non-Gaussian models, and including exchangeable and exponential decay covariance structures.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10683350PMC
http://dx.doi.org/10.1177/09622802231202379DOI Listing

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