Back to Search Start Over

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 A
Cameron, Jan
Kilkenny, Monique F
Andrew, Nadine E
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
Butler, Ernest
Ma, Henry
Churilov, Leonid
Source :
International Journal of Stroke. Feb2022, Vol. 17 Issue 2, p236-241. 6p.
Publication Year :
2022

Abstract

Rationale: To address unmet needs, electronic messages to support person-centered 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 randomization. Methods and design: Multicenter, double-blind, randomized controlled trial with intention-to-treat analysis. The intervention group receives 12 weeks of personalized, goal-centered, and administrative electronic messages, while the control group only receive 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. Randomization: 1:1 computer-generated, stratified by age and baseline disability. Outcomes assessments: Collected at 90 days and 12 months following randomization. Outcomes: Primary outcomes include hospital emergency presentations/admissions within 90 days of randomization. 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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17474930
Volume :
17
Issue :
2
Database :
Academic Search Index
Journal :
International Journal of Stroke
Publication Type :
Academic Journal
Accession number :
155129058
Full Text :
https://doi.org/10.1177/17474930211022678