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Taking people in South KoreaNo phase

Arm and hand exercises with focused vibration for people after a stroke

Tests arm training with added vibration versus training alone in stroke survivors.

Plain-language title generated from the registry record
Registry title: Task-Oriented Upper Limb Training With Focal Vibration in Stroke

Key facts

Where
Seoul, South KoreaSee the 2 sites

Where in South Korea

  • Cheongdam HospitalSeoul, South KoreaTaking people
  • Sahmyook UniversitySeoul, South KoreaNot yet recruiting

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Jisu Kim
Trial code
NCT07558876
Record updated
16 October 2026
Original description
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.Read full original descriptionShow less

Effects of Task-Oriented Upper Limb Training With Localized Vibration on Hand Function, Proprioception, and Muscle Tone in Patients With Stroke

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.

Inclusion: Individuals diagnosed with stroke at least 3 months prior; Individuals with sufficient cognitive function (Mini-Mental State Examination [MMSE] score ≥ 24); Individuals able to maintain a seated position independently and perform upper limb functional tasks (Trunk Control Test [TCT] ≥ 50); Individuals with muscle tone of the affected upper limb of Modified Ashworth Scale (MAS) Grade ≤ 2; Individuals with Fugl-Meyer Assessment-Upper Extremity (FMA-UE) scores between 20 and 50; Individuals able to grasp and move objects with the affected upper limb and with muscle strength of Manual Muscle Test (MMT) Grade ≥ 3; Individuals with impaired proprioception in the affected hand (defined as a score < 2 on the wrist or thumb position item of the FMA-UE).

Exclusion: Individuals who received treatments affecting upper limb function within the past 3 months (e.g., botulinum toxin injection, surgery, nerve block); Individuals within 3 months after stroke onset; Individuals with severe sensory hypersensitivity or complex regional pain syndrome (CRPS); Individuals with fractures, severe soft tissue injuries, or contraindications to focal vibration.

ClinicalTrials.gov NCT07558876