Improving self-management and rehabilitation for people recovering from stroke
Efficacy of the Improving Participation after Stroke Self-Management-Rehabilitation (IPASS-R) program in sub-acute stroke
This study is testing a program called IPASS-R that helps people recovering from a stroke feel more confident and improve their daily activities through virtual sessions, and it will see how well this program works compared to a general health self-management program.
Quick facts
| Grant type | R01 grant |
|---|---|
| Study type | NIH-funded research |
| Funding institution | University of Missouri-Columbia NIH-funded |
| Lab location | 1 site (Columbia, United States) |
| Project ID | NIH-10856613 on NIH RePORTER |
What this research studies
This research investigates a program called the Improving Participation after Stroke Self-Management Rehabilitation (IPASS-R) aimed at helping individuals recovering from stroke improve their self-efficacy and daily activities. The program focuses on managing stroke as a chronic condition rather than just reducing impairments. Participants will engage in virtual sessions to enhance their quality of life and community involvement. The study will compare the effectiveness of IPASS-R with a general health self-management program.
Who could benefit from this research
Good fit: Ideal candidates for this research are individuals who have experienced a subacute stroke and are living in the community.
Not a fit: Patients who are in the acute phase of stroke recovery or those with severe cognitive impairments may not benefit from this research.
Why it matters
Potential benefit: If successful, this research could significantly enhance the quality of life and daily functioning for stroke survivors.
How similar studies have performed: Previous research has shown promise in self-management interventions for chronic diseases, indicating potential success for this approach.
Where this research is happening
Columbia, United States
- University of Missouri-Columbia — Columbia, United States (Active)
Researchers
- Principal investigator: Boone, Anna — University of Missouri-Columbia
- Study coordinator: Boone, Anna
About this research
- This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
- Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
- For full project details, budget, and progress reports, visit the official NIH RePORTER page below.