NCT03655431CompletedNot Applicable
Telerehabilitation Using Kinect-based VR to Improve Mobility and Fatigue in Veterans With MS
Shane.Chanpimol2 sites in 1 country10 target enrollmentStarted: October 1, 2016Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 10
- Locations
- 2
- Primary Endpoint
- Multiple Sclerosis Walking Scale-12 (MSWS-12)
Study Overview
Brief Summary
The primary purpose of this study is to evaluate the effects of an individualized telerehabilitation program on mobility, fatigue, and quality of life for Veterans with MS. The secondary purpose was to assess adherence to exercise recommendations and overall satisfaction with the intervention.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to 65 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Clinical diagnosis of MS based on the McDonald criteria
- •Expanded Disability Status Scale (EDSS) of 3.0 - 6.5
- •Cognitive ability (Montreal Cognitive Assessment score >23/30)
- •Physician clearance for exercise participation
- •Physical therapy referral
Exclusion Criteria
- •MS-related exacerbation within last 3 months
- •Unstable cardiac or pulmonary disease
- •Active substance abuse
- •Uncontrolled seizures
Outcomes
Primary Outcomes
Multiple Sclerosis Walking Scale-12 (MSWS-12)
Time Frame: Change after 12-week intervention
This questionnaire has 12 items and measures self-reported walking ability in MS. The questions assess the limitations of a patient's walking due to MS during the past 2 weeks. Each item ranges from 1 to 5 and the higher the sum, the more severe the degree of limitation.
Secondary Outcomes
- Short Physical Performance Battery (SPPB)(Change after 12-week intervention)
- 25-Foot Walk Test (25FWT)(Change after 12-week intervention)
- Veteran Rand 12 Quality of Life Measure (VR-12)(Change after 12-week intervention)
- Modified Fatigue Impact Scale (MFIS)(Change after 12-week intervention)
Investigators
Shane.Chanpimol
Co-Investigator
Washington D.C. Veterans Affairs Medical Center
Study Sites (2)
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