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Research on the Application Mechanism of "Intention Recognition Movement Assistance" for Restoring the Function of Paralyzed Limbs After Stroke Based on Combined Decoding of Brain and Muscle Electromyography.

Research on the Application Mechanism of "Intention Recognition Movement Assistance" for Restoring the Function of Paralyzed Limbs After Stroke Based on Combined Decoding of Brain and Muscle Electromyography.

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091319
Enrollment
Unknown
Registered
2024-10-25
Start date
2024-11-01
Completion date
Unknown
Last updated
2024-10-28

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

Conditions

Stroke

Interventions

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 (cerebral infarction/cerebral hemorrhage); 2 Age is 18 years or older and 80 years or younger, with no gender restrictions; 3 The onset time for patients with cerebral infarction is more than two weeks, and for patients with cerebral hemorrhage, it is more than three weeks; 4 Right-handed; 5 Normal cognitive function (MMSE score above the critical value corresponding to different levels of education); 6 Muscle tone in the affected upper limb is grade 2 or lower; 7 Presence of hand motor dysfunction; 8 Understands and agrees to participate in this study and has signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1 Have a history of epilepsy, mental illness, or other diseases with severe cognitive or emotional functional impairments; 2 Have other diseases or factors affecting limb activity, such as fractures, severe arthritis, amputation, etc.; 3 Have a history of using drugs affecting central nervous system excitability within the past month; 4 Are women who are pregnant, breastfeeding, or planning to become pregnant; 5 Have participated in or are currently participating in other clinical trials within the last month before joining this study.

Design outcomes

Primary

MeasureTime frame
Action Research Arm Test(ARAT);

Secondary

MeasureTime frame
Brunnstrom stage;Manual muscle test;Modified Ashworth Scale (MAS);Range of motion. ROM;Mini-mental state examination, MMSE;NIH Stroke Scale, NIHSS;Barthel index;Fugl-Meyer assessment scale-upper extremity;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