Neuromuscular Electrical Stimulation on Median Nerve Facilitates Low Motor Cortex Excitability in Human With Spinocerebellar Ataxia
- Conditions
- Spinocerebellar Ataxia
- Registration Number
- NCT02103075
- Lead Sponsor
- Chang Gung University
- Brief Summary
Spinocerebellar ataxia (SCA) is a hereditary disorder with movement incoordination. The ataxia performed low intra-cortical facilitation mainly due to the degenerative cerebellum. Noninvasive sensory stimulations such as peripheral electrical stimulation were reported to modulate the excitability of the motor excitability. Neuromuscular electrical stimulation (NMES) was proposed as a neuromodulation tool for the aberrant motor excitability on the SCA. This study aims to investigate the effect of NMES on the motor excitability in the SCA, and the differentiation on the central or peripheral motor excitability changed by the NMES.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 29
- Clinical diagnosis of Spinocerebellar ataxia
- No history of epilepsy
- No other neuromuscular disorder
- No fracture within the last six months and restricted movement on the upper extremity
- Limited trembling hand allowed for the EMG recording.
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Central Motor Excitability Baseline, in experiment, 0 minute, 10 minutes, and 20 minutes. Measure of changes in Central Motor Excitability by motor evoked potential and silent period that are measured by transcranial magnetic stimulation.
Peripheral Motor Excitability Baseline, in experiment, 0 minute, 10 minutes, and 20 minutes. Measure of changes in peripheral motor excitability by Maximum M wave and H reflex
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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Trial Locations
- Locations (1)
Chang Gung University
🇨🇳Taoyuan, Taiwan
Chang Gung University🇨🇳Taoyuan, Taiwan