Skip to content

Research for Clinical Application of Remote Rehabilitation Training and Evaluation System

Research for Clinical Application of Remote Rehabilitation Training and Evaluation System

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900027178
Enrollment
Unknown
Registered
2019-11-03
Start date
2018-01-31
Completion date
Unknown
Last updated
2019-11-04

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

Conditions

Stroke

Interventions

Experimental group:Remote scene interactive rehabilitation training and intelligent evaluation
Control group:Doctor's regular on-site guidance

Sponsors

Suzhou Xiangcheng People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. It is in accordance with the diagnostic criteria of stroke and confirmed by CT or MRI; 2. Aged 30 to 75 years; 3. Secondary rehabilitation patients with limb motor dysfunction 1-6 months after stroke onset (Brunnstrom stage III-VI for motor function evaluation of hemiplegia); 4. Clear cognition, able to follow the research plan (MMSE >=24 points); 5. The subjects can understand the purpose of the study, show sufficient compliance with the study plan, and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Significant cognitive impairment that can not complete the measurement of Fugl Meyer scale; motor function evaluation of hemiplegia Brunnstrom scale grade I-II; 2. Other significant limb diseases such as fracture, severe arthritis, amputation, etc; 3. The formation of limb joint contracture; 4. The disabled patients (blind, deaf, dumb, mental disorder, mental disorder, physical disability) as prescribed by law; 5. Patients with cardiovascular, liver, kidney, hematopoietic system and other serious primary diseases and psychosis; 6. Women of childbearing age with positive urine pregnancy test results; 7. Those who can not be included in the group according to the researcher's judgment through laboratory examination and ECG examination; 8. Those who have participated in clinical trials of other drugs / devices within 3 months before screening; 9. Other conditions that the researcher thinks are not suitable for participating in the experiment; 10. Those with metal instruments in the body, such as pacemakers.

Design outcomes

Primary

MeasureTime frame
General state;Brunnstrom stage;Balance function;Muscle strength;

Countries

China

Contacts

Public ContactGuo Liquan

Suzhou Institute of Biomedical Engineering Technology

guolq@sibet.ac.cn+86 15312183986

Outcome results

None listed

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