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Recruiting NCT07641790

Effects of Wearable Vibratory Devices on Arm Function in Subacute Stroke Patients

Conditions: Hemiplegia, Stroke

Sex: All
Ages: 30 Years – 60 Years
Healthy volunteers: No
Phase: NA
Enrollment: 30
Sponsor: University of Faisalabad

Location: The University of Faisalabad Faisalābad Punjab Province

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.

Eligibility Criteria

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

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07641790). StuddyBuddy aggregates publicly available trial information.