Using virtual reality to help recover from ischemic stroke
Improving Functional and Cognitive Outcomes After Ischemic Stroke Using Virtual Reality Based Rehabilitation
This study is testing whether virtual reality therapy can help adults recovering from a stroke feel better when combined with regular physical and occupational therapy.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 15 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Stony Brook University Academic / other |
| Locations | 1 site (Stony Brook, New York) |
| Trial ID | NCT06401564 on ClinicalTrials.gov |
What this trial studies
This study explores the use of virtual reality-based rehabilitation as an additional therapy for adults recovering from acute ischemic stroke. Participants will engage in one or two virtual reality therapy sessions while receiving conventional physical and occupational therapy. The study aims to assess the feasibility and tolerability of this immersive technology in an inpatient hospital setting, with participants completing surveys after each session to provide feedback on their experience.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 who have experienced an ischemic stroke and can follow multistep commands.
Not a fit: Patients with plegia in both arms, severe pre-existing conditions, or those unable to start therapy during admission may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could enhance recovery outcomes and improve the quality of life for stroke patients.
How similar studies have performed: Other studies have shown promise in using virtual reality for rehabilitation, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age \> 18 * MRI or CT imaging confirmed ischemic stroke * Able to follow multistep commands Exclusion Criteria: * Plegia in both arms * Previous reported history of vertigo or inner ear dysfunction * Patients with epilepsy * Patients who cannot begin therapy during admission * Patients who are pregnant * Patients with a pre-existing condition that interferes with virtual reality usage (e.g., visual impairment, limitation of either upper extremity or neck).
Where this trial is running
Stony Brook, New York
- Stony Brook University Hospital — Stony Brook, New York, United States (Recruiting)
Study contacts
- Principal investigator: Jason Mathew, DO — Stony Brook University Hospital
- Study coordinator: Christine Pol, PhD
- Email: christiana.pol@stonybrookmedicine.edu
- Phone: (631) 444-9083
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.