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A study on the efficacy and underlying mechanisms of a hand exoskeleton rehabilitation training system based on brain-machine-EMG coupling for restoring hand function in stroke patients with hemiplegia

A study on the efficacy and underlying mechanisms of a hand exoskeleton rehabilitation training system based on brain-machine-EMG coupling for restoring hand function in stroke patients with hemiplegia

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088710
Enrollment
Unknown
Registered
2024-08-26
Start date
2024-09-01
Completion date
Unknown
Last updated
2024-09-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

stroke

Interventions

group 1:Physical therapy, occupational therapy, conventional rehabilitation treatments such as neural modulation, and treatment with a hand exoskeleton rehabilitation training system based on EEG-EMG

Sponsors

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Meets the diagnostic criteria for stroke (ischemic/hemorrhagic stroke); 2. Age = 18 years and = 80 years, no gender restrictions; 3. Onset of stroke between two weeks and one year prior; 4. Right-handed; 5. Normal cognitive function (MMSE score above the threshold for the corresponding educational level); 6. Able to tolerate 1-2 hours of treatment; 7. Presence of hand motor function impairment; 8. Understands, agrees to participate in this study, and signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Presence of contraindicated neural modulation implants in or on the body (e.g., ferromagnetic implants, pacemakers, etc.); 2. History of epilepsy, mental disorders, or other diseases with severe cognitive or emotional dysfunction; 3. Other conditions or factors affecting limb movement, such as fractures, severe arthritis, amputation, etc.; 4. History of using drugs that affect central nervous system excitability within the past month; 5. Women who are pregnant or breastfeeding.

Design outcomes

Primary

MeasureTime frame
Action Research Arm Test(ARAT);

Secondary

MeasureTime frame
Brunnstrom stage;Manual muscle test(MMT);Modified Ashworth Scale( MAS);Range of motion.(ROM);Minimum Mental State Examination(MMSE);NIH Stroke Scale(NIHSS);Barthel index;Fugl-Meyer assessment scale upper extremity(FMA-UE);Electromyography((EMG);Electroencephalogram(EEG);

Countries

China

Contacts

Public ContactJiajia Wu

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai

wujiajia@shutcm.edu.cn+86 151 6176 9295

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026