Feasibility and acceptability of the breakfast group intervention BISTRo for stroke survivors in acute rehabilitation.

Authors

Natalie Jones, Susan Mawson, Avril Drummond, Alicia O'Cathain

Published in

Clinical rehabilitation. Pages 2692155261476634. Aug 13, 2026. Epub Aug 13, 2026.

Abstract

ObjectiveTo examine the feasibility and acceptability of a co-designed breakfast group intervention, BISTRo, delivered within an acute stroke rehabilitation service.DesignMultisite mixed-methods feasibility study.SettingThree National Health Service stroke rehabilitation wards in the United Kingdom.ParticipantsSixteen stroke survivors and 53 multidisciplinary staff from occupational therapy, physiotherapy, speech and language therapy, dietetics, nursing, and psychology.InterventionA structured breakfast group, delivered on five mornings a week over two weeks, integrating social dining, peer support, multidisciplinary rehabilitation, and functional eating and drinking practice.MethodsAttendance, attrition, and therapy dose were recorded. Patient-reported outcomes included a self-confidence Likert scale and subscales of the Confidence after Stroke Measure. Semi-structured interviews with stroke survivors and staff focus groups explored acceptability. Qualitative data were analysed thematically using feasibility and acceptability frameworks.ResultsSixteen stroke survivors participated across all wards, with high attendance (mean 8.9 sessions/standard deviation 1.45 out of 10), no intervention-related withdrawals, and complete data collection. Fifteen participants improved on the self-confidence measure. Positive attitude scores improved in eight participants, remained stable in five, and declined in three. In interviews with stroke survivors (n = 12) and focus groups with staff (n = 21), BISTRo was described as meaningful, confidence-building, and socially supportive. Staff also reported improved interdisciplinary working and manageable resource demands.ConclusionsDelivery of the BISTRo breakfast group was feasible and acceptable and warrants further evaluation. Conducting this feasibility study has enabled identification of potential changes to the trial design.

PMID:
42593360
Bibliographic data and abstract were imported from PubMed on 13 Aug 2026.

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