Ignite Creation Date:
2024-05-05 @ 4:58 PM
Last Modification Date:
2024-10-26 @ 9:26 AM
Study NCT ID:
NCT00358865
Status:
COMPLETED
Last Update Posted:
2008-05-07
First Post:
2006-07-31
Brief Title:
Checking the Usability of a Virtual Reality System in Children With Brain Injury
Sponsor:
Sheba Medical Center
Organization:
Sheba Medical Center
Study Overview
Official Title:
Checking the Usability of Video Projected Virtual Reality Sytem in Children With Acquired Brain Injury
Status:
COMPLETED
Status Verified Date:
2008-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this study is to check the usability of Virtual Reality VR Video Capture Projected System in children with acquired brain injuryABIand comparing their performance to the performance of normally developing children The trial shall include 15 subjects in each group aged 6-12 years old ABI subjects are hospitalized at the hospitals Pediatric Rehabilitation Department Each subject will experience 3 different virtual environments The subjects in the trial group will practice 3 experiences 3 times in 3 different days during a period of a week to 10 days to check the practice effectIn addition all subjects will be tested in three tests PEDI - to evaluate the functional abilities of daily living dressing eatingThe Melbourne Assessment - to evaluate functional movements of upper extremities and the TEA-ch - to evaluate different attention abilities Performance correlations will be tested between these tests and the performance in the VR first experience
Detailed Description:
The purpose of this study is to check the usability of Virtual Reality VR Video Capture Projected System in children with acquired brain injuryABI comparing their performance with the performance of normally developing children matched by age gendersector and parents education subjects age 6 - 12 years old The trial shall include 15 subjects in each group ABI subjects are hospitalized at Sheba Hospitals Pediatric Rehabilitation Department
Each subject will experience 3 different virtual environments The subjects in the trial group will practice 3 experiences 3 times in 3 different days during a period of a week to 10 days to check the practice effect In addition all subjects will be tested in three tests PEDI - to evaluate the functional abilities of daily living dressing eatingThe Melbourne Assessment - to evaluate functional movements of upper extremities and the TEA-ch - to evaluate difference attention abilities
Correlations between those tests to the performance in the VR experiences will be checked with Pearsons statistical correlation tests The differences between the trial group ABI children and the control group will be checked with Independent t-tests
Each subject will experience 3 different virtual environments The subjects in the trial group will practice 3 experiences 3 times in 3 different days during a period of a week to 10 days to check the practice effect In addition all subjects will be tested in three tests PEDI - to evaluate the functional abilities of daily living dressing eatingThe Melbourne Assessment - to evaluate functional movements of upper extremities and the TEA-ch - to evaluate difference attention abilities
Correlations between those tests to the performance in the VR experiences will be checked with Pearsons statistical correlation tests The differences between the trial group ABI children and the control group will be checked with Independent t-tests
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None