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Process evaluations for cluster-randomised trials of complex interventions: a proposed framework for design and reporting

BACKGROUND: Process evaluations are recommended to open the ‘black box’ of complex interventions evaluated in trials, but there is limited guidance to help researchers design process evaluations. Much current literature on process evaluations of complex interventions focuses on qualitative methods,...

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Autores principales: Grant, Aileen, Treweek, Shaun, Dreischulte, Tobias, Foy, Robbie, Guthrie, Bruce
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3600672/
https://www.ncbi.nlm.nih.gov/pubmed/23311722
http://dx.doi.org/10.1186/1745-6215-14-15
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author Grant, Aileen
Treweek, Shaun
Dreischulte, Tobias
Foy, Robbie
Guthrie, Bruce
author_facet Grant, Aileen
Treweek, Shaun
Dreischulte, Tobias
Foy, Robbie
Guthrie, Bruce
author_sort Grant, Aileen
collection PubMed
description BACKGROUND: Process evaluations are recommended to open the ‘black box’ of complex interventions evaluated in trials, but there is limited guidance to help researchers design process evaluations. Much current literature on process evaluations of complex interventions focuses on qualitative methods, with less attention paid to quantitative methods. This discrepancy led us to develop our own framework for designing process evaluations of cluster-randomised controlled trials. METHODS: We reviewed recent theoretical and methodological literature and selected published process evaluations; these publications identified a need for structure to help design process evaluations. We drew upon this literature to develop a framework through iterative exchanges, and tested this against published evaluations. RESULTS: The developed framework presents a range of candidate approaches to understanding trial delivery, intervention implementation and the responses of targeted participants. We believe this framework will be useful to others designing process evaluations of complex intervention trials. We also propose key information that process evaluations could report to facilitate their identification and enhance their usefulness. CONCLUSION: There is no single best way to design and carry out a process evaluation. Researchers will be faced with choices about what questions to focus on and which methods to use. The most appropriate design depends on the purpose of the process evaluation; the framework aims to help researchers make explicit their choices of research questions and methods. TRIAL REGISTRATION: Clinicaltrials.gov NCT01425502
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spelling pubmed-36006722013-03-19 Process evaluations for cluster-randomised trials of complex interventions: a proposed framework for design and reporting Grant, Aileen Treweek, Shaun Dreischulte, Tobias Foy, Robbie Guthrie, Bruce Trials Methodology BACKGROUND: Process evaluations are recommended to open the ‘black box’ of complex interventions evaluated in trials, but there is limited guidance to help researchers design process evaluations. Much current literature on process evaluations of complex interventions focuses on qualitative methods, with less attention paid to quantitative methods. This discrepancy led us to develop our own framework for designing process evaluations of cluster-randomised controlled trials. METHODS: We reviewed recent theoretical and methodological literature and selected published process evaluations; these publications identified a need for structure to help design process evaluations. We drew upon this literature to develop a framework through iterative exchanges, and tested this against published evaluations. RESULTS: The developed framework presents a range of candidate approaches to understanding trial delivery, intervention implementation and the responses of targeted participants. We believe this framework will be useful to others designing process evaluations of complex intervention trials. We also propose key information that process evaluations could report to facilitate their identification and enhance their usefulness. CONCLUSION: There is no single best way to design and carry out a process evaluation. Researchers will be faced with choices about what questions to focus on and which methods to use. The most appropriate design depends on the purpose of the process evaluation; the framework aims to help researchers make explicit their choices of research questions and methods. TRIAL REGISTRATION: Clinicaltrials.gov NCT01425502 BioMed Central 2013-01-12 /pmc/articles/PMC3600672/ /pubmed/23311722 http://dx.doi.org/10.1186/1745-6215-14-15 Text en Copyright ©2013 Grant 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 Methodology
Grant, Aileen
Treweek, Shaun
Dreischulte, Tobias
Foy, Robbie
Guthrie, Bruce
Process evaluations for cluster-randomised trials of complex interventions: a proposed framework for design and reporting
title Process evaluations for cluster-randomised trials of complex interventions: a proposed framework for design and reporting
title_full Process evaluations for cluster-randomised trials of complex interventions: a proposed framework for design and reporting
title_fullStr Process evaluations for cluster-randomised trials of complex interventions: a proposed framework for design and reporting
title_full_unstemmed Process evaluations for cluster-randomised trials of complex interventions: a proposed framework for design and reporting
title_short Process evaluations for cluster-randomised trials of complex interventions: a proposed framework for design and reporting
title_sort process evaluations for cluster-randomised trials of complex interventions: a proposed framework for design and reporting
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3600672/
https://www.ncbi.nlm.nih.gov/pubmed/23311722
http://dx.doi.org/10.1186/1745-6215-14-15
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