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Clinical Trials/KCT0005705
KCT0005705
Completed
N/A

Effects of robot-assisted gait training using end-effector type robot (Morning Walk?) in stroke and spinal cord injury patients

Inje University Ilsan Paik Hospital0 sites182 target enrollmentTBD

Overview

Phase
N/A
Intervention
Not specified
Conditions
Diseases of the circulatory system
Sponsor
Inje University Ilsan Paik Hospital
Enrollment
182
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
December 12, 2022
Last Updated
3 years ago
Study Type
Interventional Study
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • a) Patients with stroke over the age of 19
  • b) Patients less than one year of onset
  • c) Patients with Functional Ambulatory Category score 2 or more
  • a) Patients with traumatic or non\-traumatic SCI over the age of 19
  • b) Patients less than one year of onset
  • c) Patients with upper motor neuron damage with neurological level of injury (NLI) from C2 to T12
  • d) Patients classified as the American Spinal Injury Association Impairment Scale(AIS) C or D
  • e) Patients w ho can maintain a standing position for more than 1 minute through one person’s minimal assistance, or sit to stand through one person’s moderate assistance

Exclusion Criteria

  • a) Patients with a previous history of stroke
  • b) Patients with severe communication difficulties due to cognitive impairment or aphasia
  • c) Patients with limitation in range of motion of lower limb joints
  • d) Patients at risk of fracture with severe osteoporosis
  • e) Patients with pressure ulcer on the sacrum, coccyx, ischium, etc.
  • f) Patients who had difficulty walking before a stroke
  • a) Patients with limitation in range of motion of lower limb joints
  • b) Patients at risk of fracture with severe osteoporosis
  • c) Patients with pressure ulcer on the sacrum, coccyx, ischium, etc.
  • d) Patients with difficulty in communication due to cognitive impairment

Outcomes

Primary Outcomes

Not specified

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