Evidence map›Paper›PMID 40859327›Full record

Trial reportTrials2025

Feasibility of a Study Within a Trial to evaluate a decision support intervention for families deciding about research on behalf of adults lacking capacity to consent (CONSULT SWAT).

Victoria Shepherd, Kim Smallman, Fiona Wood, Katie Gillies, Adam Martin, Maria Moore, Stacy Todd, Kerenza Hood

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Trials, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Victoria ShepherdCentre for Trials Research, Cardiff University, Wales, UK. ShepherdVL1@cardiff.ac.uk.ORCID http://orcid.org/0000-0002-7687-0817
Kim SmallmanCentre for Trials Research, Cardiff University, Wales, UK.
Fiona WoodPRIME Centre Wales, Wales, UK.
Katie GilliesAberdeen Centre for Evaluation (ACE), University of Aberdeen, Aberdeen, UK.
Adam MartinAcademic Unit of Health Economics, University of Leeds, Leeds, UK.
Maria MooreLiverpool School of Tropical Medicine, Liverpool, UK.
Stacy ToddTropical and Infectious Disease Unit, NHS University Hospitals of Liverpool, Liverpool, UK.
Kerenza HoodCentre for Trials Research, Cardiff University, Wales, UK.

Funding

HCRW_ NIHR-FS(A)-2021
6 · The paper itself

Abstract

backgroundTrials involving adults who lack capacity to consent can be challenging, partly due to the involvement of 'proxy' decision-makers. This is usually a family member, who advises the researchers about the person's wishes. Families can find decision making difficult and some experience a decisional burden. Following the development of a decision aid for family members making trial participation decisions, we are conducting a mixed-methods randomised Study Within a Trial (SWAT) to evaluate its (cost-)effectiveness. This paper reports the feasibility stage conducted in one host study to inform delivery of the main SWAT.

methodsFamily members approached to act as a consultee for the host study were randomised 1:1 to receive the decision aid booklet alongside standard study information (intervention), or standard information plus a blank notebook (control), and asked to complete the CONCORD scale (Combined Scale for Proxy Informed Consent Decisions) questions about their experience and take part in a semi-structured interview. Acceptability of the SWAT was assessed through exploring recruitment rates and data completeness, and qualitatively through interviews with family members and research staff. Interviews were analysed using a rapid qualitative approach.

resultsIn total, 92 family members were randomised to the SWAT and 16 completed the CONCORD questionnaire. Interviews were conducted with consultees (n = 4), and host study staff (n = 3) who also provided resource use data. Differences in time staff spent with consultees were small. Key themes included (1) setting up the SWAT and balancing priorities with the host study, (2) differences when recruiting consultees to a SWAT, (3) feasibility and acceptability of the SWAT, (4) challenges of measuring decision quality and (5) views and experiences of the decision support intervention.

conclusionThe CONSULT SWAT is feasible, but changes to study processes are needed in advance of the main SWAT. The findings suggest that attempting to seamlessly integrate the SWAT into the host study may have inadvertently led to it becoming 'invisible' to consultees. The small number of trials involving participants lacking capacity limits opportunities for developing the evidence-base. Recruitment of host trials continues, with a focus on evaluating the intervention in a broad range of populations and settings.

trial registrationThe SWAT is registered as SWAT #159 with the Northern Ireland Hub for Trials Methodology Research SWAT repository (registered 09.08.2020).

Indexed as

Decision MakingDecision Support TechniquesFamilyInformed ConsentMental CompetencyResearch SubjectsThird-Party ConsentAdultAgedFeasibility StudiesFemaleHealth Knowledge, Attitudes, PracticeHumansMaleMiddle AgedPamphletsClinical trialEmbedded randomised controlled trialInformed consentProxy decision makingStudy within A TrialSWAT

Identifiers

PMID40859327
PMCPMC12382041

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.