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Protocol of a randomized controlled trial investigating the effectiveness of Recovery-focused Community support to Avoid readmissions and improve Participation after Stroke (ReCAPS)

Authors :
Cadilhac, Dominique
Cameron, Jan
Kilkenny, Monique F
Andrew, Nadine Elizabeth
Harris, Dawn
Ellery, Fiona
Thrift, Amanda G
Purvis, Tara
Kneebone, Ian
Dewey, Helen
Drummond, Avril
Hackett, Maree
Grimley, Rohan
Middleton, Sandy
Thijs, Vincent
Cloud, Geoffrey
Carey, Mariko L
Butler, Ernest
Ma, Henry
Churilov, Leonid
Hankey, Graeme J
English, Coralie Kym
Lannin, Natasha A.
Cadilhac, Dominique
Cameron, Jan
Kilkenny, Monique F
Andrew, Nadine Elizabeth
Harris, Dawn
Ellery, Fiona
Thrift, Amanda G
Purvis, Tara
Kneebone, Ian
Dewey, Helen
Drummond, Avril
Hackett, Maree
Grimley, Rohan
Middleton, Sandy
Thijs, Vincent
Cloud, Geoffrey
Carey, Mariko L
Butler, Ernest
Ma, Henry
Churilov, Leonid
Hankey, Graeme J
English, Coralie Kym
Lannin, Natasha A.
Publication Year :
2021

Abstract

Rationale: To address unmet needs, electronic messages to support person-centred goal attainment and secondary prevention may avoid hospital presentations/readmissions after stroke, but evidence is limited. Hypothesis: Compared to control participants, there will be a 10% lower proportion of intervention participants who represent to hospital (emergency/admission) within 90 days of randomisation. Methods and design: Multicentre, double-blind, randomised controlled trial with intention-to-treat analysis. The intervention group receives 12 weeks of personalised, goal-centred and administrative electronic messages, while the control group only receives administrative messages. The trial includes a process evaluation, assessment of treatment fidelity and an economic evaluation. Participants: Confirmed stroke (modified Rankin Score: 0-4), aged �18 years with internet/mobile phone access, discharged directly home from hospital. Randomisation: 1:1 computer-generated, stratified by age and baseline disability. Outcomes Assessments: Collected at 90 days and 12 months following randomisation. Outcomes: Primary: Hospital emergency presentations/admissions within 90 days of randomisation. Secondary outcomes include goal attainment, self-efficacy, mood, unmet needs, disability, quality-of-life, recurrent stroke/cardiovascular events/deaths at 90 days and 12 months, and death and cost-effectiveness at 12 months. Sample size: To test our primary hypothesis, we estimated a sample size of 890 participants (445 per group) with 80% power and two-tailed significance threshold of α=0.05. Given uncertainty for the effect size of this novel intervention, the sample size will be adaptively re-estimated when outcomes for n=668 are obtained, with maximum sample capped at 1100. Discussion: We will provide new evidence on the potential effectiveness, implementation and cost-effectiveness of a tailored eHealth intervention for survivors of stroke.

Details

Database :
OAIster
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1261709702
Document Type :
Electronic Resource