Virtual Reality and Active Video Games to Improve Balance in Children With Brain Injury

Sponsor
Blythedale Children's Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT03386968
Collaborator
(none)
4
1
2
49
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Study Details

Study Description

Brief Summary

The purpose of this pilot feasibility study is to assess the feasibility of using the Playstation Xbox 360 and Rutgers V-step via a Kinect Sensor with active video game software as a part of a physical therapy intervention to improve obstacle negotiation, gait speed, and stair negotiation in ambulatory children with Cerebral Palsy (CP) hemiparesis or spastic diplegia, or non-progressive brain injury (BI). Children will be assessed using perceptual, balance, functional and gait assessments.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Active video gaming
  • Behavioral: Usual care physical therapy
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
4 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
A Randomized Block Design will be utilized in order to attempt to "match" subjects according to functional level and diagnosis (cerebral palsy or acquired brain injury). Upon signing consent the subjects will be grouped based on their diagnosis. At that time gait speed for the 10 M Walk Test will be utilized to categorize all participants into a "fast" and "slow" group. (subjects performing the 10 M Walk Test at a speed less than .4 m/s will be placed in the "slow" group, and subjects testing at a speed greater than or equal to .4 m/s will be placed in the "fast" group After this determination is made, subjects will be randomized to "control" (usual care), and "intervention" one therapy session replaced with a session utilizing Active video games and the Rutger's V-step. A minimum of 2 subjects per grouping will be sought in order to analyze for differences.A Randomized Block Design will be utilized in order to attempt to "match" subjects according to functional level and diagnosis (cerebral palsy or acquired brain injury). Upon signing consent the subjects will be grouped based on their diagnosis. At that time gait speed for the 10 M Walk Test will be utilized to categorize all participants into a "fast" and "slow" group. (subjects performing the 10 M Walk Test at a speed less than .4 m/s will be placed in the "slow" group, and subjects testing at a speed greater than or equal to .4 m/s will be placed in the "fast" group After this determination is made, subjects will be randomized to "control" (usual care), and "intervention" one therapy session replaced with a session utilizing Active video games and the Rutger's V-step. A minimum of 2 subjects per grouping will be sought in order to analyze for differences.
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Use of Low-Cost Virtual Reality and Active Video Games to Improve Balance and Perceptual Skills in Children With Cerebral Palsy and Brain Injury
Actual Study Start Date :
Dec 7, 2017
Actual Primary Completion Date :
Jan 6, 2022
Actual Study Completion Date :
Jan 6, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Video gaming

A child's usual physical therapy session will be replaced with a session utilizing Active video games and the Rutger's V-step.

Behavioral: Active video gaming
Children will visit Blythedale for 8 sessions, one 45-session visit per week, in place of one of the child's typical physical therapy sessions. During each session, children will play a video game on the X-Box Kinect system, using the games "Kinect Adventures" and "Kinect Sports". The child will first play a "Kinect Adventures" game, which requires ambulating, ducking, and dodging one's way through an obstacle course.

Active Comparator: Usual care

Children will receive their usual care in the physical therapy program at Blythedale.

Behavioral: Usual care physical therapy
Children will attend their usual care physical therapy appointments at Blythedale.

Outcome Measures

Primary Outcome Measures

  1. Change in Pediatric Evaluation of Disability Inventory Computer Adaptive Test [From before intervention to immediately after intervention]

    The PEDI-CAT measures abilities in three functional domains: Daily Activities, Mobility and Social/Cognitive.

Secondary Outcome Measures

  1. Change in 10 Meter walk test [From before intervention to immediately after intervention]

    Measures time taken for a participant to walk 10 meters

  2. Change in Gross Motor Function Measure (GMFM) subtest D and E [From before intervention to immediately after intervention]

    The GMFM is a standardized observational instrument designed and validated to measure change in gross motor function over time in children with cerebral palsy.

  3. Change in Four Square Step Test [From before intervention to immediately after intervention]

    Measures how well a patient can change directions while stepping.

  4. Change in Functional Gait Assessment (FGA) [From before intervention to immediately after intervention]

    10-item test that assesses dynamic balance and postural stability during gait.

  5. Change in Motor Free Visual Perceptual Test (MVPT)-4 [From before intervention to immediately after intervention]

    The MVPT-4 assesses five categories of visual perception: Visual Discrimination: Ability to discriminate dominant features of different objects, including the ability to discriminate position, shapes, and forms.

  6. Change in Visually guided weight shift ability as measured by the Smart Balance MasterĀ® [From before intervention to immediately after intervention]

    Force platform system that tests balance

  7. Change in Children's Assessment of Participation and Enjoyment [From before intervention to immediately after intervention]

    Self-report measures of children's participation in recreation and leisure activities outside of mandated school activities.

Eligibility Criteria

Criteria

Ages Eligible for Study:
7 Years to 17 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age 7-17

  • Diagnosis of Cerebral Palsy or Diagnosis of Acquired Brain Injury

  • Ambulatory with or without an assistive device x 150 feet

  • Cognition and attention ability sufficient to be successful in video game play and to follow instructions of the investigator.

  • Able to complete testing process.

  • Current patient at Blythedale Children's Hospital program (Expected Length of Stay/availability for study of approximately 8 weeks)

Exclusion Criteria:
  • Any history of photosensitive epilepsy or seizures triggered by exposure to flashing lights, television or video games

  • Attention or behavior problems that prevent the successful completion of game play

  • Any acute musculoskeletal injury that limits weight bearing on one lower extremity (due to orthopedist concerns for fracture or injury)

  • Any medical condition that prevents the child from tolerating exercise due to cardiovascular conditions

Contacts and Locations

Locations

Site City State Country Postal Code
1 Blythedale Children's Hospital Valhalla New York United States 10595

Sponsors and Collaborators

  • Blythedale Children's Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Blythedale Children's Hospital
ClinicalTrials.gov Identifier:
NCT03386968
Other Study ID Numbers:
  • 17-1206TS
First Posted:
Dec 29, 2017
Last Update Posted:
Jan 10, 2022
Last Verified:
Jan 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Blythedale Children's Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 10, 2022