Task-Oriented Upper Limb Training With Focal Vibration in Stroke
Condition(s) studied
Investigational drug(s) / intervention(s)
ask-oriented upper limb training combined with focal vibration: Participants in the experimental group will receive task-oriented upper limb training combined with focal vibration applied to the wrist extensor muscles during task performance. The intervention will be administered for 30 minutes per session, 2 times per week, for 6 weeks, and no vibration will be applied during rest periods.
Active Comparator: Task-Oriented Upper Limb Training Alone: Participants in the control group will receive task-oriented upper limb training without the application of focal vibration, with the device attached to the wrist extensor muscles. The intervention will be administered for 30 minutes per session, 2 times per week, for 6 weeks.
Study summary
This study aims to investigate the effects of task-oriented upper limb training combined with focal vibration on hand function, proprioception, and muscle tone in patients with stroke. Participants will be randomly assigned to either an experimental group receiving task-oriented training with concurrent focal vibration or a control group receiving task-oriented training alone. The intervention will be conducted over 6 weeks. Outcome measures will be assessed before and after the intervention.
Eligibility
Primary outcome measure(s)
- Fugl-Meyer Assessment for Upper Extremity (FMA-UE) — Baseline and immediately after 6 weeks of intervention
The Fugl-Meyer Assessment for Upper Extremity (FMA-UE) will be used to evaluate motor function of the affected upper limb. The total score ranges from 0 to 66, with higher scores indicating better motor function.
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Cheongdam Hospital | Seoul | South Korea | Recruiting |
| Sahmyook University | Seoul | South Korea | Not Yet Recruiting |
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07558876 on ClinicalTrials.gov ↗ ← All trials in South Korea