The goal of this study is to learn if the Improving Healthand Lifestyle Programme (iHeLP) is feasible and acceptable to stroke survivors. The main questions it aims to answer are: * Is iHeLP feasible to deliver? * Is iHeLP acceptable to people who take part? * What effect does iHeLP have on the lifestyle behaviours of participants? Participants will: * Take part in the iHeLP intervention (consists of a one-to-one interview with the facilitator followed by six weekly group sessions with other stroke survivors) * Complete questionnaires about their lifestyle during the one-to-one interview and after the intervention. * Participate in a focus group to discuss their experiences and perceptions of iHeLP.
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Recruitment
Timeframe: During screening to enrollment
Retention
Timeframe: From enrollment to follow-up assessments (week 8)
Adherence to the intervention schedule
Timeframe: During the intervention period (week 1 to week 8)
Intervention fidelity
Timeframe: During the intervention period (week 1 to week 8)
Adverse events
Timeframe: During the intervention period (week 1 to week 8)
Acceptability
Timeframe: Follow-up assessments (week 8)