Actively Recruiting
Motor-Cognitive Interactive Upper Limb Robot Rehabilitation for Post-Stroke Motor Dysfunction
Led by Lidian Chen · Updated on 2025-04-24
1047
Participants Needed
1
Research Sites
90 weeks
Total Duration
On this page
Sponsors
L
Lidian Chen
Lead Sponsor
F
Fujian University of Traditional Chinese Medicine Affiliated Rehabilitation Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study aims to investigate the effects of motor-cognitive interactive robot-assisted training on improving upper limb motor dysfunction after stroke. By observing different combinations of motor and cognitive components in the training, the study will clarify the relationship between the proportion of motor and cognitive elements and the recovery of upper limb motor function. The goal is to optimize the training protocol for upper limb rehabilitation robots and enhance their therapeutic outcomes. Participants will be randomly assigned to one of three groups: motor-cognitive interactive robot-assisted training, motor-focused robot-assisted training, or conventional rehabilitation training. Training sessions will last 60 minutes, occur 5 times per week, and continue for 4 weeks. Researchers will measure changes in upper limb function and monitor for any adverse events during the training.
CONDITIONS
Official Title
Motor-Cognitive Interactive Upper Limb Robot Rehabilitation for Post-Stroke Motor Dysfunction
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of stroke confirmed by CT or MRI.
- Age between 40 and 80 years, with no gender restrictions.
- First-ever stroke with unilateral limb paralysis.
- Stroke occurred between 2 weeks and 6 months ago with an Fugl-Meyer Assessment Upper Extremity score of 8-44.
- Willingness to participate and provide written informed consent.
You will not qualify if you...
- History of neuromuscular diseases, malignant tumors, or other severe uncontrolled conditions including cardiac, renal, or hepatic diseases.
- Seated balance score less than 2 or inability to maintain sitting position for more than 60 minutes.
- Modified Ashworth Scale score greater than 2.
- Visual Analog Scale score over 3 for hemiplegic shoulder pain.
- Boston Diagnostic Aphasia Examination score less than 3.
- Severe visual impairment preventing participation in robot-assisted upper limb rehabilitation.
- Hamilton Depression Scale score over 17 indicating moderate to severe depression.
- Participation in other clinical trials that could interfere with this study.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Fujian University of Traditional Chinese Medicine
Fuzhou, China, 350122
Actively Recruiting
Research Team
J
Jingsong Wu
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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