Actively Recruiting
The Neural Mechanism and Efficacy of Somatosensory Motor Integration Training on the Upper Extremity Somatosensory Motor Function in Patients With Chronic Stroke
Led by National Taiwan University Hospital · Updated on 2026-03-03
153
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
N
National Taiwan University Hospital
Lead Sponsor
N
National Science and Technology Council, Taiwan
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are investigating the effects of different training methods on upper limb function in patients who have had a stroke at least six months ago and still experience somatosensory and motor impairments. The study aims to compare somatosensory-motor integration training, pure motor training, and pure somatosensory training to understand their impact on recovery and the underlying brain mechanisms using neuroimaging and neurophysiological methods. Participants will be randomly assigned to one of three groups: somatosensory-motor integration training, pure somatosensory training, or pure motor training. Each group will receive 15 sessions of training lasting 60 minutes each, delivered three to five times per week. The somatosensory-motor integration group performs functional tasks using both hands that require somatosensory discrimination to support motor control. The pure somatosensory group focuses on somatosensory discrimination tasks with the affected hand, while the pure motor group practices bilateral task-oriented movements without somatosensory discrimination. During the study, participants will undergo baseline assessments, post-intervention evaluations, and a follow-up after three months. Researchers will measure changes in brain activity using functional near-infrared spectroscopy and assess motor and sensory functions with clinical scales such as the Action Research Arm Test and Fugl-Meyer Assessment. Additional evaluations include the quality and frequency of limb use in daily life, ability to perform daily activities, and quality of life. The study will analyze treatment effects and factors influencing recovery over the study period, which lasts up to approximately five weeks plus the three-month follow-up.
CONDITIONS
Brief Title
Effect of Somatosensory Motor Intergration Training on Post-stroke Upper Limb Function.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 20 years or older
- Diagnosed with stroke
- Stroke occurred at least 6 months ago
- Upper limb Brunnstrom stage III to V
- No severe muscle spasticity (Modified Ashworth Scale 2 or less) in the affected upper limb
- Self-perceived or therapist-assessed somatosensory impairment
You will not qualify if you...
- Significant cognitive impairment (Montreal Cognitive Assessment less than 20)
- Severe mental disorders such as schizophrenia or major depression
- Substance abuse or alcoholism
- Claustrophobia
- Severe aphasia affecting comprehension and clear expression of somatosensory information
- Hemineglect
- Other muscle or joint problems affecting upper limb function such as contractures, rheumatoid arthritis, or myositis ossificans
- Currently participating in other somatosensory or motor therapy studies
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 5 weeks
Participants receive one of three types of training: somatosensory-motor integration training, pure somatosensory training, or pure motor training. Training sessions occur 3 to 5 times per week for a total of 15 sessions.
3 to 5 sessions per week for 15 sessions
Duration - 3 months
Participants are monitored for changes in upper limb function and cerebral hemodynamics following the completion of training.
1 follow-up visit at 3 months
Trial Site Locations
Total: 1 location
1
National Taiwan University Hospital
Taipei, Taiwan, Taiwan
Actively Recruiting
Research Team
Y
Yi-jing Huang, Assistant professor
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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