Using virtual reality to help stroke patients recover upper limb function
Using Immersive Virtual Reality for the Upper Limb Rehabilitation of Post-stroke Subjects: a Multicenter Randomized Control Trial
This study tests if using virtual reality can help stroke patients improve their arm movement and regain independence in daily activities.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 48 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | University Hospital of Ferrara Academic / other |
| Locations | 1 site (Ferrara) |
| Trial ID | NCT06892886 on ClinicalTrials.gov |
What this trial studies
This study investigates the effectiveness of an immersive virtual reality system using a head-mounted display for upper limb rehabilitation in patients who have experienced a sub-acute stroke. The approach aims to simulate real-life movements and tasks to enhance motor function recovery, potentially allowing patients to regain independence in daily activities. Participants will be assessed based on their upper limb motor impairment, and the study will quantitatively measure improvements in limb functioning. The goal is to provide clearer evidence on the benefits of virtual reality in stroke rehabilitation.
Who should consider this trial
Good fit: Ideal candidates are individuals who have suffered a first ischemic or hemorrhagic stroke within the last four weeks and have upper limb motor impairment.
Not a fit: Patients with additional neurological conditions, severe cognitive impairments, or significant upper-limb pain may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve upper limb recovery and quality of life for stroke survivors.
How similar studies have performed: While the use of virtual reality in rehabilitation is a growing field, the specific application in upper limb recovery for sub-acute stroke patients is still being explored, indicating a mix of novel and previously tested approaches.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * diagnosis of first, ischemic or hemorrhagic, stroke verified by brain imaging within 4 week * upper limb motor impairment defined by an upper extremity score \<55 on the Fugl-Meyer Assessment Exclusion Criteria: * neurological conditions in addition to stroke that may affect motor function * other medical conditions likely to interfere with the ability to safely complete the study protocol * impaired cognitive functioning that influences the ability to give informed consent * severe neuropsychological disorders * visual impairment * severe upper-limb pain defined as \> 7 on the Visual Analogue Scale
Where this trial is running
Ferrara
- Ferrara University Hospital — Ferrara, Italy (Recruiting)
Study contacts
- Study coordinator: Sofia Straudi, MD, PhD
- Email: sofia.straudi@unife.it
- Phone: +390532238720
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.