Strategies to enhance recruitment and consent to intensive care studies: a qualitative study with researchers and patient-public involvement contributors.

adult intensive & critical care intensive & critical care qualitative research

Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
22 09 2021
Historique:
entrez: 23 9 2021
pubmed: 24 9 2021
medline: 3 11 2021
Statut: epublish

Résumé

Clinical trials and studies in intensive care units (ICUs) have complex consent processes and often encounter problems in recruiting patients. By interviewing research team members about the challenges in critical care research, we aimed to identify strategies to enhance recruitment and consent to ICU studies. Semistructured interviews with UK-based researchers (N=17) and patient-public involvement (PPI) contributors (N=8) with experience of ICU studies. Analysis of transcripts of audio-recorded interviews drew on thematic approaches. Seven themes were identified. Participants emphasised the need for substitute decision-making processes in critical care studies, yet some researchers reported that research ethics committees (RECs) were reluctant to approve such processes. Researchers spoke about the potential benefits of research without prior consent (RWPC) for studies with narrow recruitment windows but believed RECs would not approve them. Participants indicated that the activity of PPI contributors was limited in critical care studies, though researchers who had involved PPI contributors more extensively were clear that their input when designing consent processes was important. Researchers and PPI contributors pointed to resource and staffing limitations as barriers to patient recruitment. Researchers varied in whether and how they used professional consultees as substitute decision-makers, in whether they approached families by telephone to discuss research and in whether they disclosed details of research participation to bereaved relatives. Critical care research could benefit from RECs having expertise in consent processes that are suited to this setting, better staffing at research sites, more extensive PPI and an evidence base on stakeholder perspectives on critical care research processes. Guidance on professional consultee processes, telephoning relatives to discuss research, RWPC and disclosure of research participation to bereaved relatives could help to harmonise practice in these areas and enhance recruitment and consent to critical care studies.

Identifiants

pubmed: 34551943
pii: bmjopen-2020-048193
doi: 10.1136/bmjopen-2020-048193
pmc: PMC8461270
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e048193

Informations de copyright

© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Katie Paddock (K)

Faculty of Health and Education, School of Childhood, Youth and Education Studies, Manchester Metropolitan University, Manchester, UK k.paddock@mmu.ac.uk.
Institute of Population Health, Department of Public Health, Policy and Systems, University of Liverpool, Liverpool, UK.

Kerry Woolfall (K)

Institute of Population Health, Department of Public Health, Policy and Systems, University of Liverpool, Liverpool, UK.

Lucy Frith (L)

Faculty of Humanities and Social Sciences, Department of Law and Philosophy, University of Liverpool, Liverpool, UK.

Megan Watkins (M)

Institute of Population Health, Department of Public Health, Policy and Systems, University of Liverpool, Liverpool, UK.

Carrol Gamble (C)

Institute of Population Health, Department of Biostatistics, University of Liverpool, Liverpool, UK.

Ingeborg Welters (I)

Institute of Life Course and Medical Science, University of Liverpool, Liverpool, UK.
Department of Critical Care, Liverpool University Hospitals NHS Foundation Trust, Liverpool, UK.

Bridget Young (B)

Institute of Population Health, Department of Public Health, Policy and Systems, University of Liverpool, Liverpool, UK.

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Classifications MeSH