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Equipoise across the patient population: optimising recruitment to a randomised controlled trial

BACKGROUND: This paper proposes a novel perspective on the value of qualitative research for improving trial design and optimising recruitment. We report findings from a qualitative study set within the OPEN trial, a surgical randomised controlled trial (RCT) comparing two interventions for recurren...

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Autores principales: Whybrow, Paul, Pickard, Robert, Hrisos, Susan, Rapley, Tim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5369002/
https://www.ncbi.nlm.nih.gov/pubmed/28347354
http://dx.doi.org/10.1186/s13063-016-1711-8
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author Whybrow, Paul
Pickard, Robert
Hrisos, Susan
Rapley, Tim
author_facet Whybrow, Paul
Pickard, Robert
Hrisos, Susan
Rapley, Tim
author_sort Whybrow, Paul
collection PubMed
description BACKGROUND: This paper proposes a novel perspective on the value of qualitative research for improving trial design and optimising recruitment. We report findings from a qualitative study set within the OPEN trial, a surgical randomised controlled trial (RCT) comparing two interventions for recurrent bulbar urethral stricture, a common cause of urinary problems in men. METHODS: Interviews were conducted with men meeting trial eligibility criteria (n = 19) to explore reasons for accepting or declining participation and with operating urologists (n = 15) to explore trial acceptability. RESULTS: Patients expressed various preferences and understood these in the context of relative severity and tolerability of their symptoms. Accounts suggest a common trajectory of worsening symptoms with a particular window within which either treatment arm would be considered acceptable. Interviews with clinician recruiters found that uncertainty varied between general and specialist sites, which reflect clinicians’ relative exposure to different proportions of the patient population. CONCLUSION: Recruitment post referral, at specialist sites, was challenging due to patient (and clinician) expectations. Trial design, particularly where there are fixed points for recruitment along the care pathway, can enable or constrain the possibilities for effective accrual depending on how it aligns with the optimum point of patient equipoise. Qualitative recruitment investigations, often focussed on information provision and patient engagement, may also look to better understand the target patient population in order to optimise the point at which patients are approached. TRIAL REGISTRATION: ISRCTN Registry, ISRCTN98009168. Registered on 29 November 2012.
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spelling pubmed-53690022017-03-30 Equipoise across the patient population: optimising recruitment to a randomised controlled trial Whybrow, Paul Pickard, Robert Hrisos, Susan Rapley, Tim Trials Research BACKGROUND: This paper proposes a novel perspective on the value of qualitative research for improving trial design and optimising recruitment. We report findings from a qualitative study set within the OPEN trial, a surgical randomised controlled trial (RCT) comparing two interventions for recurrent bulbar urethral stricture, a common cause of urinary problems in men. METHODS: Interviews were conducted with men meeting trial eligibility criteria (n = 19) to explore reasons for accepting or declining participation and with operating urologists (n = 15) to explore trial acceptability. RESULTS: Patients expressed various preferences and understood these in the context of relative severity and tolerability of their symptoms. Accounts suggest a common trajectory of worsening symptoms with a particular window within which either treatment arm would be considered acceptable. Interviews with clinician recruiters found that uncertainty varied between general and specialist sites, which reflect clinicians’ relative exposure to different proportions of the patient population. CONCLUSION: Recruitment post referral, at specialist sites, was challenging due to patient (and clinician) expectations. Trial design, particularly where there are fixed points for recruitment along the care pathway, can enable or constrain the possibilities for effective accrual depending on how it aligns with the optimum point of patient equipoise. Qualitative recruitment investigations, often focussed on information provision and patient engagement, may also look to better understand the target patient population in order to optimise the point at which patients are approached. TRIAL REGISTRATION: ISRCTN Registry, ISRCTN98009168. Registered on 29 November 2012. BioMed Central 2017-03-27 /pmc/articles/PMC5369002/ /pubmed/28347354 http://dx.doi.org/10.1186/s13063-016-1711-8 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Whybrow, Paul
Pickard, Robert
Hrisos, Susan
Rapley, Tim
Equipoise across the patient population: optimising recruitment to a randomised controlled trial
title Equipoise across the patient population: optimising recruitment to a randomised controlled trial
title_full Equipoise across the patient population: optimising recruitment to a randomised controlled trial
title_fullStr Equipoise across the patient population: optimising recruitment to a randomised controlled trial
title_full_unstemmed Equipoise across the patient population: optimising recruitment to a randomised controlled trial
title_short Equipoise across the patient population: optimising recruitment to a randomised controlled trial
title_sort equipoise across the patient population: optimising recruitment to a randomised controlled trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5369002/
https://www.ncbi.nlm.nih.gov/pubmed/28347354
http://dx.doi.org/10.1186/s13063-016-1711-8
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