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Clinical Trials/KCT0007230
KCT0007230
Not yet recruiting
未知

Comparative analysis study on passive and active robotic devices to change arm functionality through proximal upper extremity assistance in patients with spinal cord injury

ational Rehabilitation Center0 sites60 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
ational Rehabilitation Center
Enrollment
60
Status
Not yet recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional Study
Sex
All

Investigators

Sponsor
ational Rehabilitation Center

Eligibility Criteria

Inclusion Criteria

  • 1\. Chronic patients more than 3 months after onset
  • 2\. Tetraplegia patients (C2\-T1\)
  • 3\. A patient with weakness in the muscle strength of the proximal part of the upper extremity.
  • 4\. If the proximal part of the upper extremity is good, endurance is low, and there is a limitation in performing daily activities such as eating and grooming.
  • 5\. Patients with shoulder and elbow range of motion of more than 90 degrees and 50 degrees, respectively.
  • 6\. Those who can sit tolerance for more than 30 minutes.

Exclusion Criteria

  • 1\. Those with severe contracture problems in the upper extremities
  • 2\. Patients with obvious diseases that can cause muscle weakness due to abnormalities in the central nervous system other than spinal cord injury (eg, neuromyalgia)
  • 3\. Those who have difficulty following the therapist's instructions due to cognitive problems.
  • 4\. Those who have limited upper extremity movement due to stiffness of MAS 3 or higher
  • 5\. A person who can independently carry out daily life activities

Outcomes

Primary Outcomes

Not specified

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