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      Efficient design of cluster randomized trials with treatment‐dependent costs and treatment‐dependent unknown variances

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          Abstract

          Cluster randomized trials evaluate the effect of a treatment on persons nested within clusters, where treatment is randomly assigned to clusters. Current equations for the optimal sample size at the cluster and person level assume that the outcome variances and/or the study costs are known and homogeneous between treatment arms. This paper presents efficient yet robust designs for cluster randomized trials with treatment‐dependent costs and treatment‐dependent unknown variances, and compares these with 2 practical designs. First, the maximin design (MMD) is derived, which maximizes the minimum efficiency (minimizes the maximum sampling variance) of the treatment effect estimator over a range of treatment‐to‐control variance ratios. The MMD is then compared with the optimal design for homogeneous variances and costs (balanced design), and with that for homogeneous variances and treatment‐dependent costs (cost‐considered design). The results show that the balanced design is the MMD if the treatment‐to control cost ratio is the same at both design levels (cluster, person) and within the range for the treatment‐to‐control variance ratio. It still is highly efficient and better than the cost‐considered design if the cost ratio is within the range for the squared variance ratio. Outside that range, the cost‐considered design is better and highly efficient, but it is not the MMD. An example shows sample size calculation for the MMD, and the computer code (SPSS and R) is provided as supplementary material. The MMD is recommended for trial planning if the study costs are treatment‐dependent and homogeneity of variances cannot be assumed.

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          Intraclass Correlation Values for Planning Group-Randomized Trials in Education

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            Synthesis of variance

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              Lessons for cluster randomized trials in the twenty-first century: a systematic review of trials in primary care.

              Evidence suggests that cluster randomized trials are often poorly designed and analysed. There is little recent research on the methodologic quality of cluster randomized trials and none focuses on primary health care where these trials are increasingly common. We conducted a systematic review of recent cluster randomized trials in primary health care, searching the Cochrane Controlled Trials Register. We also searched for unpublished trials in conference proceedings, and the UK National Research Register. We assess methodologic quality using a checklist, articulate problems facing investigators conducting these trials, and examine the extent to which carrying out a cluster randomized trial (as opposed to an individually randomized trial) in primary care may reduce power. We found 367 trial reports. Many trials were reported more than once. We characterize 152 independent cluster randomized trials in primary health care published between 1997 and 2000, and briefly describe 47 trials unpublished at December 2000. The quality of design and analysis was variable. Of published trials reporting sample size calculations 20% accounted for clustering in these calculations, 59% of published trials accounted for clustering in analyses. Unpublished trials were more recent and of higher quality. Reporting quality was better in journals reporting more cluster randomized trials. Many trial investigators reported problems with adherence to protocol, recruitment and type of intervention. Methodologic quality of cluster randomized trials in primary health care is variable and reporting needs improvement. The use of cluster randomization should be indicated in the title or abstract so these kinds of trials are easier to identify. Communicating appropriate methodology to health care researchers continues to be a challenge. Cluster randomized trials should always be piloted and information from pilots and unsuccessful trials shared more widely.
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                Author and article information

                Contributors
                gerard.vbreukelen@maastrichtuniversity.nl
                Journal
                Stat Med
                Stat Med
                10.1002/(ISSN)1097-0258
                SIM
                Statistics in Medicine
                John Wiley and Sons Inc. (Hoboken )
                0277-6715
                1097-0258
                10 June 2018
                20 September 2018
                : 37
                : 21 ( doiID: 10.1002/sim.v37.21 )
                : 3027-3046
                Affiliations
                [ 1 ] Department of Methodology and Statistics, CAPHRI Care and Public Health Research Institute Maastricht University PO Box 616 6200 MD The Netherlands
                [ 2 ] Department of Methodology and Statistics, Graduate School of Psychology and Neuroscience Maastricht University PO Box 616 6200 MD The Netherlands
                Author notes
                [*] [* ] Correspondence

                Gerard J.P. van Breukelen, Department of Methodology and Statistics, CAPHRI Care and Public Health Research Institute, Maastricht University, PO Box 616, 6200 MD, The Netherlands.

                Email: gerard.vbreukelen@ 123456maastrichtuniversity.nl

                Author information
                http://orcid.org/0000-0003-0949-0272
                http://orcid.org/0000-0002-2229-1131
                Article
                SIM7824 SIM-17-0659.R1
                10.1002/sim.7824
                6120518
                29888393
                093a567c-dfb7-4278-ac00-72ca9a702511
                © 2018 The Authors. Statistics in Medicine published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 13 September 2017
                : 23 March 2018
                : 19 April 2018
                Page count
                Figures: 4, Tables: 4, Pages: 20, Words: 8982
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                sim7824
                20 September 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:version=5.4.7.1 mode:remove_FC converted:03.09.2018

                Biostatistics
                cluster randomized trial,heterogeneous variance,maximin design,optimal design,sample size,study costs

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