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The difference of patients' performance in rehabilitation training assisted by robot or therapist

The difference of patients' performance in rehabilitation training assisted by robot or therapist

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078160
Enrollment
Unknown
Registered
2023-11-30
Start date
2023-11-30
Completion date
Unknown
Last updated
2023-12-03

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

Conditions

Stroke

Interventions

Test Group 1:The first day is upper limb rehabilitation training led by rehabilitation physicians, and the second day is upper limb rehabilitation training led by robots.
Test Group 2:The first day is robot led upper limb rehabilitation training, and the second day is upper limb rehabilitation training led by rehabilitation physicians.

Sponsors

Department of Mechanical Engineering, Tsinghua University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Patients with first-onset stroke who have clear MRI or CT medical imaging diagnosis of one cerebral hemisphere injury; (2) At least 4 days after the onset of the disease (at this time, most stroke patients show decreased motivation for rehabilitation training); (3) fugl-meyer's upper limb motor function score was between 20 and 35 (the scale's upper limb motor function score range was 0-66); (4) The Modified Ashworth Scale (MAS) rating was below 2, and there was no obvious spasm; (5) There is no cognitive dysfunction, can understand and follow the instructions of the experimenter to complete the training content.

Exclusion criteria

Exclusion criteria: 1) Aphasia, severe cognitive impairment, severe depression, etc.; 2) Unstable condition, including postural hypotension, septicemia, epilepsy, etc. 4) Patients with upper limb spasm, shoulder, elbow or wrist Ashworth spasm of the affected limb is greater than grade 2; 5) Function decline or failure of heart, lung, liver, kidney and other important organs; 6) Wear a pacemaker, have metal implants in the skull, or have skull defects; 7) Severe cervical spondylosis, including severe cervical spinal stenosis and cervical instability.

Design outcomes

Primary

MeasureTime frame
electroencephalogram;Positive and Negative Affect Schedule,PANAS;Doctor-patient relationship PDRQ-15 score;Kinematics and dynamics parameters of robot platform trajectory rendering;the Pittsburgh Rehabilitation Participation Scale,PRPS;

Secondary

MeasureTime frame
electrocardiogram;electrodermatogram;electromyogram;

Countries

China

Contacts

Public ContactJia Tianyu

Department of Mechanical Engineering, Tsinghua University

jiatianyu@tsinghua.edu.cn+86 188 1304 8642

Outcome results

None listed

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