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Intelligent adaptation and demonstration application of assistive devices for daily life and sports rehabilitation

Intelligent adaptation and demonstration application of assistive devices for daily life and sports rehabilitation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102745
Enrollment
Unknown
Registered
2025-05-19
Start date
2023-09-15
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Stroke

Interventions

Bilateral training group:Repetitive distal hand training is performed by a non-blinded therapist in a bilateral, simultaneous manner and consists of a set of customized exercises based on motor relear
Unilateral training group:Repetitive distal hand training is performed by an unblinded therapist in a unilateral manner and consists of a set of customized exercises based on motor relearning programs

Sponsors

The First Affiliated Hospital of Jinan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Cerebral infarction or cerebral hemorrhage confirmed by CT and/or MRI of the head in accordance with the "Diagnostic Criteria for Cerebrovascular Disease" of the Chinese Medical Association, including cortical lesions; (2) Age 18-75 years old; (3) duration of onset: 3 weeks to 6 months; (4) FMA-UE is on a score of 20-50 (moderate impairment); (5) Possess sufficient verbal and neurocognitive skills to understand instructions.

Exclusion criteria

Exclusion criteria: 1. Severe heart, liver and kidney dysfunction; 2. Visual impairment; 3. Hearing impairment; 4. Complete aphasia; 5. Severe cognitive impairment; 6. Inability to cooperate with treatment; 7. and unstable condition. Contraindications to transcranial magnetic stimulation will also be excluded if the patient has the following contraindications: (1) metal implants of any size in the head and neck; (2) Have a history of epilepsy, convulsions, or convulsions; (3) Previous head trauma or history of concussion with loss of consciousness; (4) cochlear implantation; (5) Have a history of persistent headache; (6) A pacemaker is installed in the body.

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer Assessment (FMA);

Secondary

MeasureTime frame
Maximum electromyography value;Joint range of motion;Interhemispheric inhibition;

Countries

China

Contacts

Public ContactZhuoming Chen

The First Affiliated Hospital of Jinan University

zm120tchzm@qq.com+86 133 9269 2183

Outcome results

None listed

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