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Clinical Trials/NCT01225120
NCT01225120
Unknown
Not Applicable

Amputee Gait Training Using Virtual Reality and Real-Time Feedback

Brooke Army Medical Center1 site in 1 country66 target enrollmentAugust 2007

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Abnormal Gait Kinematics
Sponsor
Brooke Army Medical Center
Enrollment
66
Locations
1
Primary Endpoint
Gait Biomechanics
Last Updated
15 years ago

Overview

Brief Summary

The purpose of this repeated measures design gait training study is to develop and quantitatively assess the effectiveness of a virtual reality training environment using real-time feedback for modification of pelvic motion during gait.

Registry
clinicaltrials.gov
Start Date
August 2007
End Date
September 2011
Last Updated
15 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Unilateral traumatic trans-tibial or transfemoral amputation
  • Independent ambulation without an assistive device for a minimum of three months
  • Ability to ambulate continuously for a minimum of 15 minutes
  • Trans-femoral participants must use an ischial containment socket
  • VAS Pain scores on the involved side of less than 4/10
  • Sagittal plane ankle, knee and hip strength of 4 or greater on the uninvolved side as determined by manual muscle test.

Exclusion Criteria

  • Blindness
  • TBI-Glascow Coma Scale score of 12 or lower at the time of injury
  • Cardiac or pulmonary problems limiting physical activity
  • PTSD or other psychological condition with symptoms that would be exacerbated by participation in the study.

Outcomes

Primary Outcomes

Gait Biomechanics

Time Frame: 3 weeks from initial post training

Study Sites (1)

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