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Robot-assisted rehabilitation scenarios for hemiplegic patients refined assessment of muscle status

Robot-assisted rehabilitation scenarios for hemiplegic patients refined assessment of muscle status

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300079211
Enrollment
Unknown
Registered
2023-12-27
Start date
2023-12-27
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

Upper limb dysfunction in hemiplegic patients

Interventions

hemiplegia group:NA

Sponsors

The First Affiliated Hospital of Naval Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for healthy subjects (1) Physical health without functional motor disorders of the upper limbs; (2) Age 18-85 years old; (3) Consciousness, good cardiorespiratory fitness, and ability to cooperate with the training program. Inclusion criteria for hemiplegic subjects (1) Hemiplegic patients with FMA upper limb function score between 0-55; (2) Age 18-85 years old; (3) Consciousness, good cardiopulmonary function, stable vital signs, and ability to cooperate with the training program.

Exclusion criteria

Exclusion criteria: Exclusion Criteria Subjects meeting any of the following criteria will be excluded from this study. (1) Lack of informed consent; (2) Implanted pacemakers or defibrillators; (3) Patients with hemiplegia who are unable to perform motor rehabilitation; (4) Patients with hemiplegia in the flaccid stage; (5) Patients with unhealed fractures, severe osteoporosis, and venous thrombosis; (6) Patients with severe hypertension (systolic blood pressure >200mmHg, diastolic blood pressure >110mmHg), diabetes mellitus with poor glycemic control or major diseases combined with dysfunction of liver, kidney, heart and other important organs; (7) Severe shoulder, elbow, and wrist passive joint mobility limitation; (8) Persons with severe impairment in vision, hearing or comprehension; (9) Those who will have an allergic reaction, hypersensitive reaction or intolerance to the rehabilitation equipment.

Design outcomes

Primary

MeasureTime frame
AAC, MAV, RMS of sEMG;Photoplethysmogram , PPG;

Countries

CHINA

Contacts

Public ContactFang Fanfu

The First Affiliated Hospital of Naval Military Medical University

fangfanfu@126.com+86 158 0071 9913

Outcome results

None listed

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