- Title
- What do stroke survivors' value about participating in research and what are the most important research problems related to stroke or transient ischemic attack (TIA)? A survey
- Creator
- Weerasekara, Ishanka; Baye, Jasmine; English, Coralie; Burke, Meredith; Crowfoot, Gary; Mason, Gillian; Peak, Rachael; Simpson, Dawn; Walker, Frederick Rohan; Nilsson, Michael; Pollack, Michael
- Relation
- BMC Medical Research Methodology Vol. 21, Issue 10 October 2021, no. 209
- Publisher Link
- http://dx.doi.org/10.1186/s12874-021-01390-y
- Publisher
- Biomed Central (BMC)
- Resource Type
- journal article
- Date
- 2021
- Description
- Background: Recruitment to stroke clinical trials is challenging, but consumer registers can facilitate participation. Researchers need to understand the key factors that facilitate trial involvement and improve consumer partnerships to identify what research topics important to stroke and transient ischemic attack (TIA) survivors and their carers. We aimed to examine i) the experience of being involved in a stroke research register, and ii) the priorities for stroke research from the perspective of stroke survivors. Methods: Online and paper-based surveys were sent directly to members of a stroke register and disseminated online. Multiple choice questions were reported as counts and percentages and open-ended questions were thematically analysed using Braun and Clarke’s 6-stage process. Results: Of 445 survey respondents, 154 (38%) were a member of the Stroke Research Register. The most frequently reported reason for research participation was to help others in the future. Respondents reported they were less likely to take part in research if the research question was not relevant to them, if transport was an issue, or because they lacked time. The most important research problems reported were targeting specific impairments including recovery of movement, fatigue, and aphasia, improvement of mental health services, and increased support for carers. Conclusions: Recruitment to trials may be improved by research registers if an inclusive research culture is fostered, in which consumers feel valued as members of a community, have direct and timely access to research findings and the opportunity to be meaningfully involved in research around the problems that consumers find most important.
- Subject
- stroke; key factors; research culture; consumers
- Identifier
- http://hdl.handle.net/1959.13/1450812
- Identifier
- uon:44024
- Identifier
- ISSN:1471-2288
- Language
- eng
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