Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT00748995 · ClinicalTrials.gov registry record
Neuropsychological and Mental Outcomes of Operation Iraqi Freedom (OIF): A Longitudinal Cohort Study
A clinical trial of Stress Disorders, Post-Traumatic, sponsored by VA Office of Research and Development.
- Active
- Registry status
- 817
- Enrollment target
- 4
- Study locations
NCT00748995 is a study of Stress Disorders, Post-Traumatic that is active but no longer recruiting, run by VA Office of Research and Development. The registered enrollment target is 817 participants, above the 143-participant average among 64 other Stress Disorders, Post-Traumatic trials with a reported enrollment target (471% higher). The trial reports 4 study locations across 3 states.
The verdict
NCT00748995, a study of Stress Disorders, Post-Traumatic, is active but no longer recruiting, sponsored by VA Office of Research and Development.
- ACTIVE NOT RECRUITING
- Registry status
- 817 participants
- Enrollment target
- 4
- Study locations
Study Summary
This is a research study examining health effects of the Iraq War, especially those effects involving mental health. This study is a follow-up to the Neurocognition Deployment Health Study (NDHS), also called "Prospective Assessment of Neurocognition in Future Gulf-deployed and Gulf-nondeployed Military Personnel: A Pilot Study." The specific purpose of this research study is to find out more about the longer lasting effects of war on mood and stress symptoms, thinking and reaction skills, and different aspects of day to day life, such as work and daily activities. Survey and test results from previous participation in the NDHS will be compared to the new information that will be obtained from participants as part of this study. The investigators expect that a total of about 817 military personnel and military Veterans will participate in the study. There are two parts to this study: (1) mail/internet/phone survey and (2) in-person assessment. The investigators will invite all NDHS participants who deployed to Iraq to participate in the survey component. The survey component of the study involves being interviewed by phone about mood and stress symptoms and head injuries and completing written survey questions by either mail or on the internet that address basic personal history (such as age, military status, gender, combat injury history), mood, stress symptoms, and stressful experiences. The phone interview will take about 2 to 2.5 hours to complete. The questionnaire part will take about 20 to 30 minutes to complete, and can be completed either by mailing back completed questionnaires or by internet using a private, individual log-in/password combination. The investigators will invite approximately 200 selected at random from the larger group of survey responders to take part in the in-person assessment. The in-person assessment involves taking a small subset of neuropsychological tasks. The tasks will be given on a computer or using paper and pencil. Participant
Conditions Studied
Study Locations (4)
Massachusetts
- VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA - Boston
- VA Medical Center, Jamaica Plain Campus - Boston
Connecticut
- CERC (VISN1, West Haven, CT) - West Haven
Washington
- VA Puget Sound Health Care System, Seattle - Seattle
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 817 participants |
| Start Date | 2010-08-31 |
| Est. Completion | 2026-09-30 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00748995
The ClinicalTrials.gov registry entry for NCT00748995 describes a study currently listed as active not recruiting, categorized as an unspecified phase. The registered enrollment target is 817 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 143-participant average among 64 other Stress Disorders, Post-Traumatic trials with a reported enrollment target (471% higher). The listed sponsor is VA Office of Research and Development, which has 1,668 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Stress Disorders, Post-Traumatic appearing as the primary indexed condition, and to 0 interventions.
NCT00748995 reports 4 study locations spanning 3 distinct geographic areas - top geographies include Massachusetts, Connecticut, Washington.
Frequently Asked Questions
What is clinical trial NCT00748995 about?
NCT00748995 is a clinical study titled "Neuropsychological and Mental Outcomes of Operation Iraqi Freedom (OIF): A Longitudinal Cohort Study". This is a research study examining health effects of the Iraq War, especially those effects involving mental health. This study is a follow-up to the Neurocognition Deployment Health Study (NDHS), also called "Prospective Assessment of Neurocognition in Future Gulf-deployed and Gulf-nondeployed Mili...
What is the current status of trial NCT00748995?
This trial is currently active not recruiting. The enrollment target is 817 participants. The study started on 2010-08-31. Estimated completion is 2026-09-30.
What conditions does trial NCT00748995 study?
This clinical trial studies the following conditions: Stress Disorders, Post-Traumatic.
Who is sponsoring clinical trial NCT00748995?
This trial is sponsored by VA Office of Research and Development, which has 1,668 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00748995 being conducted?
This trial has 4 study locations across Connecticut, Massachusetts, Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Stress Disorders, Post-Traumatic
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
-
Manage Emotions to Reduce Aggression (MERA)
RECRUITING · NA
-
SMART Therapist Training: A Hybrid Factorial-SMART Design
RECRUITING · NA
-
Overcontrol and Suicide in PTSD
RECRUITING
-
Postpartum Care in the NICU (PeliCaN) Transitions
RECRUITING · NA
-
Healthy Recovery After Trauma Study
RECRUITING · NA
-
MDMA for Co-occurring PTSD and OUD After Childbirth
RECRUITING · Phase 2
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.