- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02043834
Virtual Reality-based Exercise in Older Adults
Promoting Virtual Reality-based Exercise to Prevent Falls in Older Adults: Pilot Study
The aim of the present study is to evaluate an innovative virtual reality-based balance training intervention for improving clinically relevant motor performances (balance and gait) in older adults.
We hypothesize that the virtual reality-based balance training intervention will improve balance and gait performances in older adults compared to a control group receiving usual care only.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Arizona
-
Tucson, Arizona, United States, 85710
- Villa Hermosa - Senior Living Tucson
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- ability to ambulate without assistance
- willingness to provide informed consent
Exclusion Criteria:
- severe neurologic, cardiovascular, metabolic, or psychiatric disorders
- severe visual impairment
- cognitive impairment
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Balance Training
Balance training will be conducted individually two times per week for 4 weeks.
Each training session will include virtual reality tasks such as "ankle reaching" and "obstacle crossing" using a virtual obstacle shown on a computer screen.
Each session will last 30 - 45 minutes.
|
Balance training will be conducted individually two times per week for 4 weeks.
Each training session will include virtual reality tasks such as "ankle reaching" and "obstacle crossing" using a virtual obstacle shown on a computer screen.
Each session will last 30 - 45 minutes.
|
|
No Intervention: Control
The control group will keep their normal activity without receiving any intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Postural Balance
Time Frame: after 4 weeks
|
Postural Balance during quiet standing for 30 seconds will be assessed using validated wearable sensor technologies (BalanSens™)
|
after 4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Gait performance
Time Frame: 4 weeks
|
Gait performance will be measured using validated wearable sensor technology (LEGSys™)
|
4 weeks
|
|
Quality of life
Time Frame: 4 weeks
|
4 weeks
|
|
|
Cognitive status
Time Frame: 4 weeks
|
Changes in cognitive status will be measured by the Trail Making Test and the Category Fluency Test
|
4 weeks
|
|
Functional performance
Time Frame: 4 weeks
|
Functional performance will be assessed using the Timed Up and Go Test and the Alternate Step Test
|
4 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Bijan Najafi, PhD, interdisciplinary Consortium on Advanced Motion Performance (iCAMP), Department of Surgery, College of Medicine, University of Arizona
- Principal Investigator: Michael Schwenk, PhD, interdisciplinary Consortium on Advanced Motion Performance (iCAMP), Department of Surgery, College of Medicine, University of Arizon
Publications and 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 (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- ARPF-123
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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