Comment Period Extended to 3/23/2015 for Notice of Proposed Rulemaking (NPRM) for FDAAA 801 and NIH Draft Reporting Policy for NIH-Funded Trials

Follow-up of Psychological and Neurocognitive Gulf War Outcome: Relation to Stress

This study has been completed.
Information provided by:
Department of Veterans Affairs Identifier:
First received: July 3, 2001
Last updated: January 20, 2009
Last verified: December 2004

This is the follow-up to an observational epidemiological study of psychological and neuropsychological outcomes of deployed and non-deployed Gulf War-era veterans.

Gulf War Syndrome

Study Type: Observational
Official Title: Follow-up of Psychological and Neurocognitive Gulf War Outcome: Relation to Stress

Further study details as provided by Department of Veterans Affairs:

Study Start Date: April 1999
Estimated Study Completion Date: March 2003
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.


Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes

Participation in Time 1 data collection

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT00018707

United States, Louisiana
VA, New Orleans
New Orleans, Louisiana, United States, 70112
Sponsors and Collaborators
  More Information

No publications provided Identifier: NCT00018707     History of Changes
Other Study ID Numbers: MHBS-033-98F
Study First Received: July 3, 2001
Last Updated: January 20, 2009
Health Authority: United States: Federal Government processed this record on March 01, 2015