Follow-up of Psychological and Neurocognitive Gulf War Outcome: Relation to Stress
Primary Purpose
Gulf War Syndrome
Status
Completed
Phase
Locations
United States
Study Type
Observational
Intervention
Sponsored by
About this trial
This is an observational trial for Gulf War Syndrome
Eligibility Criteria
Participation in Time 1 data collection
Sites / Locations
- VA, New Orleans
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT00018707
First Posted
July 3, 2001
Last Updated
January 20, 2009
Sponsor
US Department of Veterans Affairs
1. Study Identification
Unique Protocol Identification Number
NCT00018707
Brief Title
Follow-up of Psychological and Neurocognitive Gulf War Outcome: Relation to Stress
Official Title
Follow-up of Psychological and Neurocognitive Gulf War Outcome: Relation to Stress
Study Type
Observational
2. Study Status
Record Verification Date
December 2004
Overall Recruitment Status
Completed
Study Start Date
April 1999 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
March 2003 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
US Department of Veterans Affairs
4. Oversight
5. Study Description
Brief Summary
This is the follow-up to an observational epidemiological study of psychological and neuropsychological outcomes of deployed and non-deployed Gulf War-era veterans.
Detailed Description
Approximately 800 deployed and 250 nondeployed veterans were originally administered psychological assessment instruments shortly after the cessation of the Gulf War. These veterans are currently being followed to evaluate longer-term psychological outcomes in relation to war-zone stress, intervening life stress, and individual difference factors and personal resources, such as coping and social support.
Approximately 75 of these veterans, oversampled for post-traumatic stress disorder, were administered a specialized neuropsychological battery emphasizing attention and memory. This sample will also be followed to evaluate longitudinal neuropsychological outcome in relation to PTSD status.
A cross-sectional study will also be conducted examining visual, hierarchical attention in relation to PTSD diagnosis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gulf War Syndrome
7. Study Design
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Participation in Time 1 data collection
Facility Information:
Facility Name
VA, New Orleans
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70112
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Follow-up of Psychological and Neurocognitive Gulf War Outcome: Relation to Stress
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