- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01414686
Virtual Environment Rehabilitation for Chronic Stroke (VEHAB)
Commercially-Available Interactive Video Games for Individuals With Chronic Mobility and Balance Deficits Post-Stroke
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Objective: To determine if playing active video games results in improved balance and motor performance.
Design: Randomized-matched, single-blind, control group cross-over study Setting: Laboratory Patients: Participants with chronic hemiparesis post-stroke were randomly assigned to a gaming group or normal activity control group.
Interventions: Gaming systems provided an interactive interface of real-time movement of either themselves or an avatar on the screen. Participants played games 1 hour/day, 4 days/week, for 5 weeks, totaling 20 hours of game-play. The intervention was strictly game-play without physical therapy. All games were played in standing position and trainers supervised to protect against loss of balance.
Measurements: Both groups were tested prior to and following the 5 weeks (post-test) and 3 months following the completion of the intervention/control. Outcome measures included: Fugl-Meyer Motor Exam, Single Leg Stance time, symmetrical weight bearing, Berg Balance Scale, Dynamic Gait Index, Timed Up and Go, Six Minute Walk, 3 Meter Walk, step length differential, and perception of recovery.
Study Type
Enrollment (Actual)
Phase
- Phase 2
Contacts and Locations
Study Locations
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South Carolina
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Columbia, South Carolina, United States, 29208
- University of South Carolina - Public Health Research Building
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Greater than 6 months following stroke
- Ability to walk 10 feet with or without assistance
- 18 years of age or older
- Clinical presentation of unilateral hemiplegia post-stroke
- Ability to follow simple two-step instructions
Exclusion Criteria:
- Unable to ambulate 150 feet prior to stroke
- History of serious chronic obstructive pulmonary disease or oxygen dependence
- Severe weight bearing pain
- Lower-extremity amputation
- Non-healing ulcers on the lower extremity
- Renal dialysis or end stage liver disease
- Legal blindness or deafness or severe visual or hearing impairment
- A history of significant psychiatric illness defined by diagnosis of bipolar affective disorder, psychosis, or schizophrenia
- Life expectancy less than one year
- Severe arthritis or orthopaedic problems that limit passive ranges of motion of lower extremity: Knee flexion contracture of -10 degrees, Knee flexion ROM < 90 degrees, hip flexion contracture > 25 degrees, ankle plantar flexion contracture > 15 degrees
- History of deep venous thrombosis or pulmonary embolism within 6 months
- Uncontrollable diabetes: diabetic coma, frequent insulin reactions
- Severe hypertension with systolic > 200mmHg and diastolic > 110mmHg at rest
- Intracranial hemorrhage related to aneurysm rupture or an arteriovenous malformation (hemorrhagic infarctions will not be excluded)
- History of severe seizure disorder; other neurological conditions such as multiple sclerosis or Parkinson's Disease
- Pain that is scored greater than 5 out of 10 on a visual analog scale and limits daily activity
- Any health problems judged by their screening physician to put the client at significant risk of harm during the study
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: CROSSOVER
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Immediate Treatment Group
|
Two commercially available gaming platforms were used in this study, the Nintendo Wii and the Sony PS 2. The Wii games included "Wii Sports" and "Wii Fit"; PS games included the EyeToy "Play 2" and "Kinetic". Each of these games provides multiple mini games which pose different movement challenges, including dynamic balance, speed, accuracy, general mobility, and weight shifts. Game play was performed 1 hour/day, 4 days/ week, for a period of 5 weeks, totaling 20 hours.
Other Names:
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NO_INTERVENTION: Delayed Treatment Group
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Balance (Berg Balance Scale)
Time Frame: change from pre to post and change from pre to follow-up (3 months)
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Do determine the influence of active gaming on balance in individuals with chronic stroke
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change from pre to post and change from pre to follow-up (3 months)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
balance (Berg Balance Scale)
Time Frame: change from pre to post and change from pre to follow-up (3 months)
|
Determine whether the Nintendo Wii games or the Sony PlayStation 2 EyeToy a) offers superior improvement of balance
|
change from pre to post and change from pre to follow-up (3 months)
|
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balance (Berg Balance Scale)
Time Frame: post (5 weeks)
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Determine whether individuals with low or high fall risk show greater improvements in balance following participation in an interactive video game session.
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post (5 weeks)
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Participant Perception
Time Frame: Post test (5 weeks)
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Determine whether the Nintendo Wii games or the Sony PlayStation 2 EyeToy offers superior participant perception of 1) enjoyability of the game, 2) feasibility for independent use of the game, and 3) improvement in perceived mobility as a result of the game.
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Post test (5 weeks)
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Stacy L Fritz, PhD, University of South Carolina
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Pro00001904
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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