Ignite Creation Date:
2024-05-05 @ 5:25 PM
Last Modification Date:
2024-10-26 @ 9:31 AM
Study NCT ID:
NCT00454454
Status:
COMPLETED
Last Update Posted:
2013-07-30
First Post:
2007-03-28
Brief Title:
Virtual Reality Helmet to Test for Problems With Memory
Sponsor:
Emory University
Organization:
Emory University
Study Overview
Official Title:
Display Enhanced TEsting for Cognitive Impairment and Traumatic Brain Injury
Status:
COMPLETED
Status Verified Date:
2013-07
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:
DETECT
Brief Summary:
The purpose of this research study is to compare a virtual reality display device with the standard neuropsychological evaluation for detecting mild cognitive impairment problems with memory concentration reaction time etc
Detailed Description:
Since many individuals with mild cognitive impairment MCI appear to function normally MCI may often be recognizable through testing in advance of any changes noticed by family members or caregivers Early and frequent testing can therefore trigger an earlier diagnosis which may increase the effectiveness of currently available medications used to delay onset of Alzheimers symptoms Primary care and geriatric physicians currently lack the necessary tools required for quick and accurate MCI screening in the doctors office environment The current industry-standard is a battery of pen paper neuropsychological tests that require 15 hours in a quiet room with a neuropsychologist
Comparison virtual reality display device compared to the standard neuropsychological evaluation for detecting mild cognitive impairment problems with memory concentration reaction time etc
Comparison virtual reality display device compared to the standard neuropsychological evaluation for detecting mild cognitive impairment problems with memory concentration reaction time etc
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