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An Exploratory Study on the Upper Limb Motor Function Rehabilitation of Stroke Based on the Integrated Robotic Technology of Vitality and Electric Dynamics and Brain-Computer Interface

Dynamic and electric integrated robot technology for limb motor function reconstruction

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100044492
Enrollment
Unknown
Registered
2021-03-23
Start date
2021-03-23
Completion date
Unknown
Last updated
2022-01-24

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

Conditions

stroke

Interventions

experimental group:BCI therapy

Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. The onset time was 2 weeks to 1 year and the disease was stable; 2. Patients with first and unilateral cerebral infarction confirmed by cranial computed tomography (CT) or magnetic resonance imaging (MRI) (diagnosis is in line with the consensus of "Key Diagnostics of Various Major Cerebrovascular Diseases in China 2019" formulated by Cerebrovascular Group of Neurology Society of Chinese Medical Association); 3. Age 18 to 75 years old (including 18 and 75 years old); 4. The Fugl-Meyer Assessment Upper Limb scale (FMA-UL) score is = 22; 7. Those who signed the informed consent after being selected.

Exclusion criteria

Exclusion criteria: 1. Patients receiving other non-invasive brain Stimulation interventions, such as Transcranial Magnetic Stimulation (TMS) or Transcranial direct-current Stimulation (TDCS); 2. Poor compliance; 3. With other serious medical diseases (such as heart failure, respiratory failure, renal insufficiency, uncontrollable hypertension, arrhythmia, severe coronary heart disease, diabetes complications poorly controlled); 4. With any acute or chronic infection (such as tuberculosis, intracranial infection, etc.); 5. Pregnancy; 6. Participants in other clinical trials at the same time; 7. Those with junior high school education level or below.

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer assessment scale;

Secondary

MeasureTime frame
Action Research Arm Test;EEG;modified Barthel index;NIHSS;rs-fMRI;DTI;

Countries

China

Contacts

Public ContactJia Jie

Huashan Hospital, Fudan University

shannonjj@126.com+86 13611722357

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 9, 2026