- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01780792
Examining the Effects of Video-game Exercise on Mobility and Brain Plasticity in Individuals With Multiple Sclerosis
Examining the Effects of Dance, Dance Revolution on Mobility, Brain Plasticity and Cognition in Individuals With Multiple Sclerosis
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Dance Dance Revolution (DDR) may offer an innovative and highly effective format for delivering exercise programs to people with MS. It is a fun, engaging and interactive video game that requires players to move their feet to targets while matching the rhythm of a song. In addition, DDR, involving both aerobic exercise and cognitive training, is an ideal intervention for improving cognitive functioning in those with MS. The purpose of this pilot study is to examine the use of DDR as a novel and highly specific exercise intervention to improve mobility and cognition among individuals with MS. We will be guided by the following three specific aims and hypotheses:
Specific Aim 1: Determine if an eight-week exercise program administered using DDR improves dynamic balance in people with MS relative to a wait-list control group.
Hypothesis 1: Dynamic balance as measured by the Berg Balance Scale will be more improved with the DDR intervention than the wait-list control group.
Specific Aim 2: Determine if the DDR intervention, combining fitness and cognitive training, over the course of an eight-week intervention, will have a more positive effect on domains of processing speed and executive control, than a wait-list control group.
Hypothesis 2: The DDR group relative to the wait-list control group, will show significant improvement in cognitive functioning as assessed by the Paced Auditory Serial Addition Test (PASAT), a measure of processing speed, and executive functioning. Specifically, we hypothesize that given severe deficits in processing speed and executive control, participation in a DDR intervention, will result in a significant improvement on the PASAT, a widely used measure to assess cognitive functioning in patients with MS.
Specific Aim 3: We will also examine whether improvements in cognitive processes engendered by DDR on the PASAT will be supported by changes in underlying neural circuits, as inferred from patterns of event-related functional magnetic resonance imaging (fMRI) activation obtained in a 3 Tesla scanner.
Hypothesis 3: Improvements in cognition as indexed by higher accuracy scores and faster reaction time on the PASAT, will be accompanied by a change in the recruitment of underlying neural processes as inferred from functional magnetic resonance imaging. MS participants in the DDR group will show an increase in recruitment of the attentional network, and more specifically the prefrontal and parietal cortices, cortical regions responsible for successful performance on the PASAT task.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Ohio
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Columbus, Ohio, United States, 43210
- The Ohio State University Atwell Hall
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Expanded Disability Status Score of < 5 and a diagnosis of relapsing-remitting multiple sclerosis
Exclusion Criteria:
- other neurological or orthopedic diagnosis that limits ambulation, age 30-59
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: Dance Dance Revolution game play
Dance Dance Revolution video game play
|
Individuals play dance dance revolution 3 times a week for 8 weeks
|
|
No Intervention: control
individuals continue usual care for 8 weeks
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Berg Balance Scale
Time Frame: after 8 weeks
|
The Berg Balance scale consists of 14 functional activities that test static and dynamic balance.
Each item is scored on a scale of 0-4 with higher scores indicating better balance
|
after 8 weeks
|
|
PASAT
Time Frame: after 8 weeks
|
The PASAT is a measure of sustained attention, working memory and information processing speed.
|
after 8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
4 square step test
Time Frame: after 8 weeks
|
requires a person to step rapidly in a multi-directional pattern over a cane.
It predicts fallers
|
after 8 weeks
|
|
The Activities Specific Balance Confidence Scale
Time Frame: after 8 weeks
|
Measures fear of falling.
Subjects rate their balance confidence on 10 items.
|
after 8 weeks
|
|
GAITRite
Time Frame: after 8 weeks
|
individuals walk on a computerized carpet that records spatiotemporal aspects of gait such as velocity and stride length.
|
after 8 weeks
|
|
6 minute walk test
Time Frame: Immediately prior to starting the intervention/control period,, after 8 week intervention/control period and then at an 8 week follow up
|
subjects walk for 6 minutes and distance walked is measured
|
Immediately prior to starting the intervention/control period,, after 8 week intervention/control period and then at an 8 week follow up
|
|
physical activity
Time Frame: after 8 weeks
|
subjects wear an accelerometer for 5 days which records how active they are.
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after 8 weeks
|
|
multiple sclerosis quality of life inventory
Time Frame: after 8 weeks
|
the MS quality of life inventory is filled out to measure the impact of MS on the individuals quality of life.
|
after 8 weeks
|
|
fMRI
Time Frame: after 8 weeks
|
individuals will go into an MRI and undergo neuropsychological and motor testing to examine for neuroplasticity
|
after 8 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ruchika Prakash, PhD, Ohio State University
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
- 2011H0048
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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