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Effect of Combined Upper Limb Rehabilitation Robot for Patients with Spinal Cord Injury

Not Applicable
Completed
Conditions
Diseases of the nervous system
Registration Number
KCT0004499
Lead Sponsor
ational Rehabilitation Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
30
Inclusion Criteria

Adults over 19 years old
Patients with cervical cord injury less than 24 months of onset (C2-C8)
American spinal injury association impairment scale (AIS) A-D
Patients with 2(poor) or more points on the manual muscle test (MMT) assessment of wrist and finger muscles
Patients with cognitive function enough to understand the contents of this study and follow the researcher's instructions
Patients who decide to participate directly with their or their parents' consent

Exclusion Criteria

Patients with obvious diseases that may cause muscle weakness beyond the central nervous system other than spinal cord injury (e.g. neuromuscular disease)
Patients with severe upper extremity stiffness above MAS 3
Patients who are restricted from sitting in wheelchairs or chairs for more than 30 minutes
Patients with severe shoulder pain
Patients with an upper ROM limit of more than 50%
Patients unable to follow the researcher's instructions due to cognitive decline

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Graded and Redefined Assessment of strength, sensibility and prehension(GRASSP)
Secondary Outcome Measures
NameTimeMethod
ASIA-upper extremity motor score(UEMS);Korean Version of Spinal Cord Independence Measure-III;Grip and pinch strength
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