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. 2010 Jul 6:10:63.
doi: 10.1186/1471-2288-10-63.

A systematic review of models to predict recruitment to multicentre clinical trials

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A systematic review of models to predict recruitment to multicentre clinical trials

Katharine D Barnard et al. BMC Med Res Methodol. .

Abstract

Background: Less than one third of publicly funded trials managed to recruit according to their original plan often resulting in request for additional funding and/or time extensions. The aim was to identify models which might be useful to a major public funder of randomised controlled trials when estimating likely time requirements for recruiting trial participants. The requirements of a useful model were identified as usability, based on experience, able to reflect time trends, accounting for centre recruitment and contribution to a commissioning decision.

Methods: A systematic review of English language articles using MEDLINE and EMBASE. Search terms included: randomised controlled trial, patient, accrual, predict, enroll, models, statistical; Bayes Theorem; Decision Theory; Monte Carlo Method and Poisson. Only studies discussing prediction of recruitment to trials using a modelling approach were included. Information was extracted from articles by one author, and checked by a second, using a pre-defined form.

Results: Out of 326 identified abstracts, only 8 met all the inclusion criteria. Of these 8 studies examined, there are five major classes of model discussed: the unconditional model, the conditional model, the Poisson model, Bayesian models and Monte Carlo simulation of Markov models. None of these meet all the pre-identified needs of the funder.

Conclusions: To meet the needs of a number of research programmes, a new model is required as a matter of importance. Any model chosen should be validated against both retrospective and prospective data, to ensure the predictions it gives are superior to those currently used.

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References

    1. Campbell MK, Snowdon C, Francis D, Elbourne D, McDonald AM, Knight R, Entwistle V, Garcia J, Roberts I, Grant A. Recruitment to randomised trials: strategies for trial enrollment and participation study. The STEPS study. Health technology assessment (Winchester, England) 2007;11:iii. ix-105. - PubMed
    1. K B. Pharma giants risk reputation through clinical trial cost-cutting. http://www.in-pharmatechnologist.com - PubMed
    1. Carter RE, Sonne SC, Brady KT. Practical considerations for estimating clinical trial accrual periods: application to a multi-center effectiveness study. BMC medical research methodology. 2005;5:11. doi: 10.1186/1471-2288-5-11. - DOI - PMC - PubMed
    1. Carter RE. Application of stochastic processes to participant recruitment in clinical trials. Controlled clinical trials. 2004;25:429–436. doi: 10.1016/j.cct.2004.07.002. - DOI - PubMed
    1. Moher D, Liberati A, Tetzlaff J, Altman DG. Group PRISMA. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. BMJ. 2009;339:b2535. doi: 10.1136/bmj.b2535. - DOI - PMC - PubMed

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