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Behavioural optimisation to address trial conduct challenges: case study in the UK-REBOA trial

BACKGROUND: Clinical trials comprise multiple processes at various stages of the trial lifecycle. These processes often involve complex behaviours such as recruiting vulnerable patient populations and clinicians having to deliver complex trial interventions successfully. Few studies have utilised a...

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Autores principales: Lawrie, Louisa, Duncan, Eilidh M., Jansen, Jan O., Campbell, Marion K., Brunsdon, Dan, Skea, Zoë, Coffey, Taylor, Cochran, Claire, Gillies, Katie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9097042/
https://www.ncbi.nlm.nih.gov/pubmed/35550599
http://dx.doi.org/10.1186/s13063-022-06341-6
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author Lawrie, Louisa
Duncan, Eilidh M.
Jansen, Jan O.
Campbell, Marion K.
Brunsdon, Dan
Skea, Zoë
Coffey, Taylor
Cochran, Claire
Gillies, Katie
author_facet Lawrie, Louisa
Duncan, Eilidh M.
Jansen, Jan O.
Campbell, Marion K.
Brunsdon, Dan
Skea, Zoë
Coffey, Taylor
Cochran, Claire
Gillies, Katie
author_sort Lawrie, Louisa
collection PubMed
description BACKGROUND: Clinical trials comprise multiple processes at various stages of the trial lifecycle. These processes often involve complex behaviours such as recruiting vulnerable patient populations and clinicians having to deliver complex trial interventions successfully. Few studies have utilised a behavioural framework to assess challenges and develop strategies for effective trial recruitment and delivery of trial interventions. This study reports the application of an innovative methodological approach to understand core trial processes, namely recruitment and intervention delivery, using a behavioural science approach to develop strategies designed to mitigate trial process problems. METHODS: The UK-REBOA trial aims to evaluate the clinical and cost-effectiveness of resuscitative endovascular balloon occlusion of the aorta (a novel intervention) in injured patients with exsanguinating haemorrhage. A behavioural investigation (‘diagnosis’) was conducted using theory-informed (Theoretical Domains Framework, TDF) semi-structured interviews with site staff from the UK-REBOA trial to examine trial processes which could be improved in relation to trial recruitment and delivery of the intervention. Interviews were analysed using the TDF to identify influences on behaviour, which were then mapped to techniques for behaviour change and developed into potential solutions. RESULTS: The behavioural diagnosis of the challenges experienced during trial processes highlighted factors relevant to a range of TDF domains: Skills, Environmental context and resources, Beliefs about capabilities, Beliefs about consequences, Social influences, and Memory, attention, and decision-making processes. Within the solution development phase, we identified 24 suitable behaviour change techniques that were developed into proposed solutions to target reported process problems with the aim of changing behaviour to improve recruitment and/or intervention delivery. Proposed solutions included targeted changes to trial training content, suggestions to restructure the environment (e.g. reinforced the purpose of the trial with information about the social and environmental consequences) and other strategies to reduce barriers to recruitment and intervention delivery. CONCLUSIONS: This study demonstrates the feasibility of applying a behavioural approach to investigate (‘diagnose’) behavioural trial process problems and subsequently develop and implement targeted solutions (‘treatment’) in an active trauma trial. Understanding the factors that affected behaviour, attitudes and beliefs in this trauma trial allowed us to implement theoretically informed, evidence-based solutions designed to enhance trial practices. TRIAL REGISTRATION: ISRCTN 16,184,981  SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13063-022-06341-6.
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spelling pubmed-90970422022-05-13 Behavioural optimisation to address trial conduct challenges: case study in the UK-REBOA trial Lawrie, Louisa Duncan, Eilidh M. Jansen, Jan O. Campbell, Marion K. Brunsdon, Dan Skea, Zoë Coffey, Taylor Cochran, Claire Gillies, Katie Trials Research BACKGROUND: Clinical trials comprise multiple processes at various stages of the trial lifecycle. These processes often involve complex behaviours such as recruiting vulnerable patient populations and clinicians having to deliver complex trial interventions successfully. Few studies have utilised a behavioural framework to assess challenges and develop strategies for effective trial recruitment and delivery of trial interventions. This study reports the application of an innovative methodological approach to understand core trial processes, namely recruitment and intervention delivery, using a behavioural science approach to develop strategies designed to mitigate trial process problems. METHODS: The UK-REBOA trial aims to evaluate the clinical and cost-effectiveness of resuscitative endovascular balloon occlusion of the aorta (a novel intervention) in injured patients with exsanguinating haemorrhage. A behavioural investigation (‘diagnosis’) was conducted using theory-informed (Theoretical Domains Framework, TDF) semi-structured interviews with site staff from the UK-REBOA trial to examine trial processes which could be improved in relation to trial recruitment and delivery of the intervention. Interviews were analysed using the TDF to identify influences on behaviour, which were then mapped to techniques for behaviour change and developed into potential solutions. RESULTS: The behavioural diagnosis of the challenges experienced during trial processes highlighted factors relevant to a range of TDF domains: Skills, Environmental context and resources, Beliefs about capabilities, Beliefs about consequences, Social influences, and Memory, attention, and decision-making processes. Within the solution development phase, we identified 24 suitable behaviour change techniques that were developed into proposed solutions to target reported process problems with the aim of changing behaviour to improve recruitment and/or intervention delivery. Proposed solutions included targeted changes to trial training content, suggestions to restructure the environment (e.g. reinforced the purpose of the trial with information about the social and environmental consequences) and other strategies to reduce barriers to recruitment and intervention delivery. CONCLUSIONS: This study demonstrates the feasibility of applying a behavioural approach to investigate (‘diagnose’) behavioural trial process problems and subsequently develop and implement targeted solutions (‘treatment’) in an active trauma trial. Understanding the factors that affected behaviour, attitudes and beliefs in this trauma trial allowed us to implement theoretically informed, evidence-based solutions designed to enhance trial practices. TRIAL REGISTRATION: ISRCTN 16,184,981  SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13063-022-06341-6. BioMed Central 2022-05-12 /pmc/articles/PMC9097042/ /pubmed/35550599 http://dx.doi.org/10.1186/s13063-022-06341-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Lawrie, Louisa
Duncan, Eilidh M.
Jansen, Jan O.
Campbell, Marion K.
Brunsdon, Dan
Skea, Zoë
Coffey, Taylor
Cochran, Claire
Gillies, Katie
Behavioural optimisation to address trial conduct challenges: case study in the UK-REBOA trial
title Behavioural optimisation to address trial conduct challenges: case study in the UK-REBOA trial
title_full Behavioural optimisation to address trial conduct challenges: case study in the UK-REBOA trial
title_fullStr Behavioural optimisation to address trial conduct challenges: case study in the UK-REBOA trial
title_full_unstemmed Behavioural optimisation to address trial conduct challenges: case study in the UK-REBOA trial
title_short Behavioural optimisation to address trial conduct challenges: case study in the UK-REBOA trial
title_sort behavioural optimisation to address trial conduct challenges: case study in the uk-reboa trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9097042/
https://www.ncbi.nlm.nih.gov/pubmed/35550599
http://dx.doi.org/10.1186/s13063-022-06341-6
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