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Clinical Trials/NCT03544398
NCT03544398
Unknown
Not Applicable

Comparison of Exoskeleten Assisted Gait Training With End-effector Assisted Gait Training in Spinal Cord Injury

Erenköy Physical Therapy and Rehabilitation Hospital1 site in 1 country20 target enrollmentJanuary 1, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Spinal Cord Injuries
Sponsor
Erenköy Physical Therapy and Rehabilitation Hospital
Enrollment
20
Locations
1
Primary Endpoint
FAC
Last Updated
5 years ago

Overview

Brief Summary

Aim is to compare exoskeleton assisted gait training with end-effector assisted gait training in Spinal Cord Rehabilitation

Detailed Description

It was planned to evaluate patients aged between 18 and 80 years who will admit to the robotic rehabilitation program due to spinal cord injury. Patients will divide into three groups as Exoskeleton, End-effector and conventional therapy. Exoskeleton and End-effector group will receive robotic therapy 4 days a week besides conventional treatment for 6 weeks. All groups will be evaluated at the start and end of the treatment.

Registry
clinicaltrials.gov
Start Date
January 1, 2020
End Date
June 30, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Erenköy Physical Therapy and Rehabilitation Hospital
Responsible Party
Principal Investigator
Principal Investigator

AYLİN SARI

MD

Erenköy Physical Therapy and Rehabilitation Hospital

Eligibility Criteria

Inclusion Criteria

  • Clinical diagnosis of spinal cord injury Applying to the hospital for a rehabilitation program

Exclusion Criteria

  • Inadequate body weight (obesity) Severe contractures Bone instability ( nonstable spinal cord fracture, and severe osteoporosis) Circulation problems Cardiac nonconformity Open wounds on the lower extremities or in the body where they will come into contact with the orthosis Uncoordinated, psychotic or aggressive patients Serious cognitive disorders Long-term infusion therapy Hip, knee, ankle arthrodesis Epilepsy Disproportionate limb or vertebrae, such as bone cartilage dysplasia

Outcomes

Primary Outcomes

FAC

Time Frame: Change from baseline FAC class to 6th week of therapy

functional ambulational classification scale

6MWT

Time Frame: Change from baseline 6MWT class to 6th week of therapy

6 minute walking test

10MWT

Time Frame: Change from baseline 10MWT class to 6th week of therapy

10 meter walking test

Secondary Outcomes

  • SCIM(Change Of SCIM from the beginnig to the 6th week of the therapy)
  • ASIA(Change Of ASIA scale from the beginnig to the 6th week of the therapy)

Study Sites (1)

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