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

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 e...

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Autores principales: Barnard, Katharine D, Dent, Louise, Cook, Andrew
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2908107/
https://www.ncbi.nlm.nih.gov/pubmed/20604946
http://dx.doi.org/10.1186/1471-2288-10-63
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author Barnard, Katharine D
Dent, Louise
Cook, Andrew
author_facet Barnard, Katharine D
Dent, Louise
Cook, Andrew
author_sort Barnard, Katharine D
collection PubMed
description 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, enrol, 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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spelling pubmed-29081072010-07-22 A systematic review of models to predict recruitment to multicentre clinical trials Barnard, Katharine D Dent, Louise Cook, Andrew BMC Med Res Methodol Research Article 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, enrol, 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. BioMed Central 2010-07-06 /pmc/articles/PMC2908107/ /pubmed/20604946 http://dx.doi.org/10.1186/1471-2288-10-63 Text en Copyright ©2010 Barnard et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Barnard, Katharine D
Dent, Louise
Cook, Andrew
A systematic review of models to predict recruitment to multicentre clinical trials
title A systematic review of models to predict recruitment to multicentre clinical trials
title_full A systematic review of models to predict recruitment to multicentre clinical trials
title_fullStr A systematic review of models to predict recruitment to multicentre clinical trials
title_full_unstemmed A systematic review of models to predict recruitment to multicentre clinical trials
title_short A systematic review of models to predict recruitment to multicentre clinical trials
title_sort systematic review of models to predict recruitment to multicentre clinical trials
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2908107/
https://www.ncbi.nlm.nih.gov/pubmed/20604946
http://dx.doi.org/10.1186/1471-2288-10-63
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