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Construction and clinical study of individualized brain-computer interactive rehabilitation training system based on multi-modal signal fusion and neural recombination characteristics(Study 3)

Construction and clinical study of individualized brain-computer interactive rehabilitation training system based on multi-modal signal fusion and neural recombination characteristics

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087762
Enrollment
Unknown
Registered
2024-08-02
Start date
2024-08-02
Completion date
Unknown
Last updated
2024-08-05

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

Conditions

Stroke

Interventions

General MI-BCI control group:General MI-BCI treatment (a single modal + general MI - BCI scheme, 30 minutes per times/day, 5 times per week, 2 weeks) + Conventional rehabilitation (physical factor the
Multi-modal MI-BCI treatment group:Multimodal MI - BCI treatment (multimodal + general MI - BCI scheme, 30 minutes per times/day, 5 times per week) + Conventional rehabilitation (physical factor thera
Individualized MI-BCI treatment group:Individualized MI-BCI treatment (single modality + individualized MI-BCI protocol, 30 minutes/time/day, 5 times/week, a total of 2 weeks)+ Conventional rehabilita
Multi-modal individualized MI-BCI treatment group:Multi-modal individualized MI-BCI treatment(Multimodal + individualized MI-BCI protocol, 30 minutes/time/day, 5 times/week for 2 weeks) + Conventional

Sponsors

The Seventh Affiliated Hospital of Sun Yat-sen Universit(Shenzhen)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. The diagnostic criteria of stroke formulated by the Fourth National Conference on Cerebrovascular Disease. 2. Confirmed by head CT or MRI examination for the first time, a course of 6 months or more. 3. Aged between 18 and 80, including 18 and 80 years old, gender not limited. 4. There were motor dysfunction in the upper limbs and hands after stroke. 5. Vital signs were stable. 6. All patients provided written informed consent for treatment.

Exclusion criteria

Exclusion criteria: 1. Severe cognitive dysfunction or mental disorders such as causes can't understand the instructions, and unable to cooperate. 2. A history of epilepsy. 3. With other influence the functional recovery of musculoskeletal and neurological diseases. 4. Have a malignant tumor, severe heart, liver, lung, and renal insufficiency and endocrine, hematopoiesis, immune system, severe primary disease. 5. Always have a arm fracture, severe arthritis, joint replacement, affect the function of upper limbs.

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer Upper Limb Motor Function Score;Action Research Arm Test Score;

Secondary

MeasureTime frame
fNIRS monitor brain connections under the changing situation;Brain activation fNIRS monitor the ROIs;

Countries

China

Contacts

Public ContactQiang Lin

The Seventh Affiliated Hospital of Sun Yat-sen Universit(Shenzhen)

linqiang@sysush.com+86 189 2249 7674

Outcome results

None listed

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