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A qualitative study of participants’ views on re-consent in a longitudinal biobank

BACKGROUND: Biomedical research increasingly relies on long-term studies involving use and re-use of biological samples and data stored in large repositories or “biobanks” over lengthy periods, often raising questions about whether and when a re-consenting process should be activated. We sought to i...

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Autores principales: Dixon-Woods, Mary, Kocman, David, Brewster, Liz, Willars, Janet, Laurie, Graeme, Tarrant, Carolyn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363013/
https://www.ncbi.nlm.nih.gov/pubmed/28330487
http://dx.doi.org/10.1186/s12910-017-0182-0
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author Dixon-Woods, Mary
Kocman, David
Brewster, Liz
Willars, Janet
Laurie, Graeme
Tarrant, Carolyn
author_facet Dixon-Woods, Mary
Kocman, David
Brewster, Liz
Willars, Janet
Laurie, Graeme
Tarrant, Carolyn
author_sort Dixon-Woods, Mary
collection PubMed
description BACKGROUND: Biomedical research increasingly relies on long-term studies involving use and re-use of biological samples and data stored in large repositories or “biobanks” over lengthy periods, often raising questions about whether and when a re-consenting process should be activated. We sought to investigate the views on re-consent of participants in a longitudinal biobank. METHODS: We conducted a qualitative study involving interviews with 24 people who were participating in a longitudinal biobank. Their views were elicited using a semi-structured interview schedule and scenarios based on a hypothetical biobank. Data analysis was based on the constant comparative method. RESULTS: What participants identified as requiring new consent was not a straightforward matter predictable by algorithms about the scope of the consent, but instead was contingent. They assessed whether proposed new research implied a fundamental alteration in the underlying character of the biobank and whether specific projects were within the scope of the original consent. What mattered most to them was that the cooperative bargain into which they had entered was maintained in good faith. They saw re-consent as one important safeguard in this bargain. In determining what required re-consent, they deployed two logics. First, they used a logic of boundaries, where they sought to detect any possible rupture with their existing framework of cooperation. Second, they used a logic of risk, where they assessed proposed research for any potential threats for them personally or the research endeavour. When they judged that a need for re-consent had been activated, participants saw the process as way of re-actualising and renewing the cooperative bargain. CONCLUSIONS: Participants’ perceptions of research as a process of mutual co-operation between volunteer and researcher were fundamental to their views on consent. Consenting arrangements for biobanks should respect the cooperative values that are important to participants, recognise the two logics used by research volunteers, and avoid rigidity. Agility may be favoured by tiered consent combined with strong oversight mechanisms; this approach requires evaluation.
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spelling pubmed-53630132017-03-24 A qualitative study of participants’ views on re-consent in a longitudinal biobank Dixon-Woods, Mary Kocman, David Brewster, Liz Willars, Janet Laurie, Graeme Tarrant, Carolyn BMC Med Ethics Research Article BACKGROUND: Biomedical research increasingly relies on long-term studies involving use and re-use of biological samples and data stored in large repositories or “biobanks” over lengthy periods, often raising questions about whether and when a re-consenting process should be activated. We sought to investigate the views on re-consent of participants in a longitudinal biobank. METHODS: We conducted a qualitative study involving interviews with 24 people who were participating in a longitudinal biobank. Their views were elicited using a semi-structured interview schedule and scenarios based on a hypothetical biobank. Data analysis was based on the constant comparative method. RESULTS: What participants identified as requiring new consent was not a straightforward matter predictable by algorithms about the scope of the consent, but instead was contingent. They assessed whether proposed new research implied a fundamental alteration in the underlying character of the biobank and whether specific projects were within the scope of the original consent. What mattered most to them was that the cooperative bargain into which they had entered was maintained in good faith. They saw re-consent as one important safeguard in this bargain. In determining what required re-consent, they deployed two logics. First, they used a logic of boundaries, where they sought to detect any possible rupture with their existing framework of cooperation. Second, they used a logic of risk, where they assessed proposed research for any potential threats for them personally or the research endeavour. When they judged that a need for re-consent had been activated, participants saw the process as way of re-actualising and renewing the cooperative bargain. CONCLUSIONS: Participants’ perceptions of research as a process of mutual co-operation between volunteer and researcher were fundamental to their views on consent. Consenting arrangements for biobanks should respect the cooperative values that are important to participants, recognise the two logics used by research volunteers, and avoid rigidity. Agility may be favoured by tiered consent combined with strong oversight mechanisms; this approach requires evaluation. BioMed Central 2017-03-23 /pmc/articles/PMC5363013/ /pubmed/28330487 http://dx.doi.org/10.1186/s12910-017-0182-0 Text en © The Author(s). 2017 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 Article
Dixon-Woods, Mary
Kocman, David
Brewster, Liz
Willars, Janet
Laurie, Graeme
Tarrant, Carolyn
A qualitative study of participants’ views on re-consent in a longitudinal biobank
title A qualitative study of participants’ views on re-consent in a longitudinal biobank
title_full A qualitative study of participants’ views on re-consent in a longitudinal biobank
title_fullStr A qualitative study of participants’ views on re-consent in a longitudinal biobank
title_full_unstemmed A qualitative study of participants’ views on re-consent in a longitudinal biobank
title_short A qualitative study of participants’ views on re-consent in a longitudinal biobank
title_sort qualitative study of participants’ views on re-consent in a longitudinal biobank
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363013/
https://www.ncbi.nlm.nih.gov/pubmed/28330487
http://dx.doi.org/10.1186/s12910-017-0182-0
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