Literature DB >> 27118559

The cohort multiple randomized controlled trial design: a valid and efficient alternative to pragmatic trials?

Joanne M van der Velden1, Helena M Verkooijen1,2, Danny A Young-Afat1,2, Johannes Pm Burbach1, Marco van Vulpen1, Clare Relton3,4, Carla H van Gils2, Anne M May2, Rolf Hh Groenwold2.   

Abstract

Randomized controlled trials (RCTs)-the gold standard for evaluating the effects of medical interventions-are notoriously challenging in terms of logistics, planning and costs. The cohort multiple randomized controlled trial approach is designed to facilitate randomized trials for pragmatic evaluation of (new) interventions and is a promising variation from conventional pragmatic RCTs. In this paper, we evaluate methodological challenges of conducting an RCT within a cohort. We argue that equally valid results can be obtained from trials conducted within cohorts as from pragmatic RCTs. However, whether this design is more efficient compared with conducting a pragmatic RCT depends on the amount and nature of non-compliance in the intervention arm.
© The Author 2016; all rights reserved. Published by Oxford University Press on behalf of the International Epidemiological Association.

Keywords:  Pragmatic randomized controlled trials; cohort multiple randomized controlled trial; efficiency; instrumental variable analysis; validity

Mesh:

Year:  2017        PMID: 27118559     DOI: 10.1093/ije/dyw050

Source DB:  PubMed          Journal:  Int J Epidemiol        ISSN: 0300-5771            Impact factor:   7.196


  26 in total

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4.  The role of the 17q21 genotype in the prevention of early childhood asthma and recurrent wheeze by vitamin D.

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Authors:  Anke Richters; Richard P Meijer; Niven Mehra; Joost L Boormans; Antoine G van der Heijden; Michiel S van der Heijden; Lambertus A Kiemeney; Katja K Aben
Journal:  BMJ Open       Date:  2021-05-18       Impact factor: 2.692

7.  Commentary: considerations for using the 'Trials within Cohorts' design in a clinical trial of an investigational medicinal product.

Authors:  Anna C Bibby; David J Torgerson; Samantha Leach; Helen Lewis-White; Nick A Maskell
Journal:  Trials       Date:  2018-01-08       Impact factor: 2.279

8.  The cohort multiple randomized controlled trial design was found to be highly susceptible to low statistical power and internal validity biases.

Authors:  David Reeves; Kelly Howells; Mark Sidaway; Amy Blakemore; Mark Hann; Maria Panagioti; Peter Bower
Journal:  J Clin Epidemiol       Date:  2017-12-19       Impact factor: 6.437

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Journal:  Trials       Date:  2017-10-27       Impact factor: 2.279

10.  Cohort Multiple Randomised Controlled Trials (cmRCT) design: efficient but biased? A simulation study to evaluate the feasibility of the Cluster cmRCT design.

Authors:  Alexander Pate; Jane Candlish; Matthew Sperrin; Tjeerd Pieter Van Staa
Journal:  BMC Med Res Methodol       Date:  2016-08-26       Impact factor: 4.615

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