Checking the Usability of a Virtual Reality System in Children With Brain Injury

Checking the Usability of Video Projected Virtual Reality Sytem in Children With Acquired Brain Injury

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00358865

Enrollment

Registered

2006-08-01

Start date

2005-12-31

Completion date

2006-12-31

Last updated

2008-05-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acquired Brain Injury

Keywords

Virtual Reality, ABI, Projected system

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 injury(ABI)and 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 hospital's 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, eating...),The 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 injury(ABI) comparing their performance with the performance of normally developing children, matched by age, gender,sector and parents' education. subjects' age: 6 - 12 years old. The trial shall include 15 subjects in each group. ABI subjects are hospitalized at Sheba Hospital's 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, eating...),The 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 Pearson's statistical correlation tests. The differences between the trial group (ABI children) and the control group will be checked with Independent t-tests.

Interventions

None listed

Study design

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

6 Years to 12 Years

Healthy volunteers

Yes

Inclusion criteria

(trial group) * acquired brain injury as a result of brain tumor excision intervention, traumatic brain injury, infection, vascular disorders, metabolic disorders or anoxia. * ability to move at least one of the upper extremities against gravity in a partial range of motion (MMT: -3)

Exclusion criteria

(trial group) * Significant visual limitations * Premorbid, progressive mental disorder or neurological injury * Premorbid learning disability Inclusion Criteria (control group): * healthy subjects

Countries

Israel

Outcome results