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Clinical Trials/KCT0007557
KCT0007557
Recruiting
N/A

A Translational Study of Clinical Effects of Gait Rehabilitation Robots in Children with Gait Disorders

Chungnam National University Hospital0 sites40 target enrollmentTBD

Overview

Phase
N/A
Intervention
Not specified
Conditions
Diseases of the nervous system
Sponsor
Chungnam National University Hospital
Enrollment
40
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Eligibility Criteria

Inclusion Criteria

  • Among patients who visited the Department of Rehabilitation Medicine up to 36 months after IRB approval
  • ? Patients with gait disorders caused by cerebral palsy or in\-progressive brain injury for more than 6 months
  • ? 5 years of age or older\~ 18 years of age or younger
  • ? Corresponds to levels 2 to 4 of the Great Motor Function Classification System (GMFCS) (level II to IV)
  • ? Simple instruction performance is subject to the degree of cognitive function possible
  • ? Where the person or guardian has heard the explanation of the study and agreed to participate in the study;
  • ? Height of 115 cm or more for two robots to wear

Exclusion Criteria

  • ? Subjects with intellectual disabilities to the extent that it is impossible to perform instructions during gait training and evaluation
  • ? In case of severe joint contracture (contraction of more than 20 degrees of flexion in the knee joint, and more than 40 degrees of flexion of the hip joint)
  • ? In case of severe lower extremity stiffness grade 3 or higher on the Modified Ashworth Scale on the lower extremity stiffness scale
  • ? If you have experience with lower extremity botulinum toxin treatment or lower extremity plaster fixation within 3 months from the first evaluation date
  • ? In case of orthopedic surgery on the lower extremities within 6 months from the first evaluation date
  • ? Other subjects deemed unsuitable for this study by the tester

Outcomes

Primary Outcomes

Not specified

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