Effects of Wearable Vibratory Devices on Arm Function in Subacute Stroke Patients
Hemiplegia, or paralysis of one side of the body, often results from stroke and severely limits arm function. Standard physiotherapy helps, but recovery is often slow. This study tests if adding a wearable vibratory device to standard therapy improves arm movement better than standard therapy alone. Thirty patients wit
| Condition(s) | Hemiplegia, Stroke |
|---|---|
| Status | Recruiting |
| Phase | NA |
| Study type | Interventional |
| Summary | Hemiplegia, or paralysis of one side of the body, often results from stroke and severely limits arm function. Standard physiotherapy helps, but recovery is often slow. This study tests if adding a wearable vibratory device to standard therapy improves arm movement better than standard therapy alone. Thirty patients with subacute stroke (3-6 months) will be split into two groups. One group will receive usual physiotherapy, while the other will receive usual physiotherapy plus the vibratory device for 8 weeks. Doctors will measure changes in spasticity (muscle stiffness), motor function, and daily independence before and after treatment. |
| Who can participate | Inclusion Criteria: * Unilateral hemiplegia secondary to stroke * Age between 30 and 60 years * Subacute stage (3 to 6 months post-stroke) * Fugl-Meyer Assessment (FMA) score between 20 and 50 * Able to follow simple verbal commands Exclusion Criteria: * Previous peripheral nerve injury or surgery affecting the upper limb * Fixed contractures or bony fractures in the affected limb * Complete sensory loss of the upper limb * Co-existing neurological conditions (e.g., Parkinson's, MS, Dementia) * Unstable cardiovascular conditions |
| Ages | 30 Years to 60 Years |
| Sex | All |
| Lead sponsor | University of Faisalabad |
| Locations | Faisalābad, Punjab Province, Pakistan |
| Start date | 2026-02-01 |
| NCT ID | NCT07641790 |
| Official listing | https://clinicaltrials.gov/study/NCT07641790 |