Autism Spectrum Disorder Clinical Trial
Official title:
Effect of Virtual Reality-based Training on Postural Control in Youth With Autism Spectrum Disorder
NCT number | NCT06023563 |
Other study ID # | 19116 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | May 15, 2023 |
Est. completion date | April 19, 2024 |
Verified date | June 2024 |
Source | Indiana University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The goal of this clinical trial is to assess the effect of short-term (3 days/week for 2 weeks) Virtual Reality (VR) active video gaming intervention on static and dynamic balance, versus traditional balance training exercises, in youth with ASD. The participants in the intervention group will engage in VR active video gaming using the Nintendo Switch Sports under supervision via Zoom for 6 sessions occurring over 2 weeks, from their home. While, the participants in the control group will engage in standard physical therapy exercises for balance and walking under supervision via Zoom, for 6 sessions occurring over 2 weeks, from their home. Their balance and walking will be assessed 3 times, 3-5 days before the intervention, 3-5 days after the intervention and 4-weeks after the intervention. - Participants static balance will be assessed by standing on pressure mat, under 2 conditions, eyes open and eyes closed for 30 seconds each. - The Pediatric Berg's balance Scale (PBS), a 14-point scale containing everyday activities, will be used as a clinical measure for assessing the static and dynamic balance. - 13-infra-red camera motion capture system, Qualisys, will be used for assessing the walking. The difference in the balance and walking parameters will be assessed and compared.
Status | Completed |
Enrollment | 12 |
Est. completion date | April 19, 2024 |
Est. primary completion date | April 19, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 7 Years to 22 Years |
Eligibility | Inclusion Criteria: - age 7-22 years, - existing ASD DSM-5 level 1 or 2 diagnosis confirmed by medical record/ educational services categorized under ASD/ therapeutic services categorized under ASD/ any other official document indicating the diagnosis of ASD, - able to follow instructions and - able to stand unsupported for at least 20 minutes. Exclusion Criteria: - epilepsy or other medical conditions which can be exacerbated by looking at a screen, - Uncorrected vision loss or any other eye condition prohibiting looking at the screen for a prolong time, - co-occurring musculoskeletal conditions such as joint or muscle pain or stiffness that limits mobility, implanted plates, pins, or screws that limit mobility, fractures or recent surgeries or any other physical condition that could interfere with the ability to play an active video game - co-occurring neurological conditions such as numbness or muscle weakness, temporary loss of vision, speech or strength, loss of consciousness (black out), Dizziness or lightheadedness, Impaired memory or confusion, any other cooccurring diagnosis that could be negatively impacted by playing an active video game - any other health conditions that are contraindicated to or may interfere with physical activity such as impaired hearing (uncorrected), medically documented balance disorder, Any heart condition prohibiting exercise, chronic pain or any pain at the time of testing, need assistance to stand for 20 minutes or more, - aggression or other severe behaviors that may limit the ability to safely participate in the intervention. |
Country | Name | City | State |
---|---|---|---|
United States | Indiana University Bloomington | Bloomington | Indiana |
Lead Sponsor | Collaborator |
---|---|
Indiana University |
United States,
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* Note: There are 17 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in the center of pressure movement | High resolution pressure mat containing multiple integrated sensors is used to detect center of pressure movement of the person standing on it recorded at 100 Hz | 3-5 days before the intervention, 3-5 days after the intervention and 4 weeks after the intervention | |
Primary | Change in Pediatric Berg's Balance Scale score | 14-component battery that evaluates daily living tasks such as sitting to standing, transferring from one chair to another, and sitting and standing without support. This scale is reliable and valid clinical balance assessment tool for children and youth with motor impairments. Maximum total score is 56 points and minimum total score is 0 points. Higher score indicates better balance such that increase in total score by 3.7 points indicates minimal clinically important difference. | 3-5 days before the intervention, 3-5 days after the intervention, 4 weeks after the intervention | |
Primary | Change in step length (meters) of the gait | 13-infra red camera system with 19-light reflecting passive markers recording at 100 Hz are used to measure the gait parameter: step length (meters). | 3-5 days before the intervention, 3-5 days after the intervention, 4 weeks after the intervention | |
Primary | Change in step width (meters) of the gait | 13-infra red camera system with 19-light reflecting passive markers recording at 100 Hz are used to measure the gait parameter: step width (meters). | 3-5 days before the intervention, 3-5 days after the intervention, 4 weeks after the intervention | |
Primary | Change in stride length (meters) of the gait | 13-infra red camera system with 19-light reflecting passive markers recording at 100 Hz are used to measure the gait parameter: stride length (meters). | 3-5 days before the intervention, 3-5 days after the intervention, 4 weeks after the intervention | |
Primary | Change in double support period (seconds) of the gait | 13-infra red camera system with 19-light reflecting passive markers recording at 100 Hz are used to measure the gait parameter: double support period (seconds). | 3-5 days before the intervention, 3-5 days after the intervention, 4 weeks after the intervention | |
Primary | Change in the cadence (steps/minute) of the gait | 13-infra red camera system with 19-light reflecting passive markers recording at 100 Hz are used to measure the gait parameter: cadence (number of steps/minute). | 3-5 days before the intervention, 3-5 days after the intervention, 4 weeks after the intervention | |
Primary | Change in gait velocity (meters/second) | 13-infra red camera system with 19-light reflecting passive markers recording at 100 Hz are used to measure the gait parameter: gait velocity (meters/second). | 3-5 days before the intervention, 3-5 days after the intervention, 4 weeks after the intervention |
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