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

RecruitingNAAges 30 Years - 60 YearsAllUniversity of Faisalabad
NCT07641790 on ClinicalTrials.gov โ†—
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In plain words

What the trial is, and whether it could suit you

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.

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๐Ÿ“‹ Eligibility rules (as published)
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
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What it tests

  • Wearable Focal Muscle Vibrator
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Where

1 site
The University of Faisalabad
Faisalฤbad, Pakistan
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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