Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02069873 · ClinicalTrials.gov registry record · NA

Effectiveness of Cognitive, Exposure, and Skills Group Manualized Treatments in Operations Iraqi (OIF)/Operation Enduring Freedom (OEF) Female Veterans

A NA study of Post Traumatic Stress Disorder, sponsored by New Mexico VA Healthcare System.

Completed
Registry status
NA
Development phase
86
Enrollment target
1
Study location

NCT02069873: Completed NA study of Post Traumatic Stress Disorder, sponsored by New Mexico VA Healthcare System.

NCT02069873 is a NA study of Post Traumatic Stress Disorder that has completed, run by New Mexico VA Healthcare System. The registered enrollment target is 86 participants, below the 663-participant average among 262 other Post Traumatic Stress Disorder trials with a reported enrollment target (87% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02069873, a NA study of Post Traumatic Stress Disorder, has completed, sponsored by New Mexico VA Healthcare System.

COMPLETED
Registry status
NA
Development phase
86 participants
Enrollment target
1
Study location

Study Summary

The purpose of the study is to evaluate the efficacy of a group protocol for the delivery of evidence-based therapies in comparison to a wait-list control and evaluate the relative contribution of exposure, cognitive, and skills blocks of treatment in a 16-session manualized group treatment protocol in a sample of OIF/OEF female PTSD veterans. Hyp1: Overall improvement is expected in PTSD symptoms compared to a wait-list control group; and Hyp2: the exposure and cognitive components are expected to show greater improvement in PTSD symptoms than the skills component. Significant results will establish the efficacy of a group format for evidence-based treatments for all veterans with a PTSD diagnosis. An ancillary part of the study is to examine initial neuropsychological presentation in this population and possible changes that may occur as the result of treatment.

Primary Outcome

Interview administration of the CAPS by independent assessor captures current (past month) and lifetime symptoms and diagnosis of Post-Traumatic Stress Disorder (PTSD).

Interventions

  • BEHAVIORAL 16-Week Group Treatment

Study Locations (1)

New Mexico

  • New Mexico VA Health Care System - Albuquerque

Trial Details

FieldValue
Enrollment Target 86 participants
Start Date 2008-04
Est. Completion 2013-02
Phase NA
New Mexico VA Healthcare System

3 total trials

What the finished NCT02069873 record still lists

NCT02069873 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 86 participants, a relatively small participant target, below the 663-participant average among 262 other Post Traumatic Stress Disorder trials with a reported enrollment target (87% lower).

The record links to 1 condition, with Post Traumatic Stress Disorder appearing as the primary indexed condition, and to 1 intervention - of which 16-Week Group Treatment is the first listed.

NCT02069873 reports a single indexed study location in New Mexico.

Frequently Asked Questions

What is clinical trial NCT02069873 about?

NCT02069873 is a clinical study titled "Effectiveness of Cognitive, Exposure, and Skills Group Manualized Treatments in Operations Iraqi (OIF)/Operation Enduring Freedom (OEF) Female Veterans". The purpose of the study is to evaluate the efficacy of a group protocol for the delivery of evidence-based therapies in comparison to a wait-list control and evaluate the relative contribution of exposure, cognitive, and skills blocks of treatment in a 16-session manualized group treatment protocol...

What is the current status of trial NCT02069873?

This trial is currently completed. It is a NA study. The enrollment target is 86 participants. The study started on 2008-04. Estimated completion is 2013-02.

What conditions does trial NCT02069873 study?

This clinical trial studies the following conditions: Post Traumatic Stress Disorder.

What interventions are being tested in trial NCT02069873?

The interventions under investigation include: 16-Week Group Treatment (BEHAVIORAL).

Who is sponsoring clinical trial NCT02069873?

This trial is sponsored by New Mexico VA Healthcare System, which has 3 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02069873 being conducted?

This trial has 1 study location across New Mexico. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Post Traumatic Stress Disorder

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.

Where NCT02069873's enrollment target sits among peer trials

86 127th of 262 higher than 135 of 262 other Post Traumatic Stress Disorder trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Post Traumatic Stress Disorder trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01639508 · 86 participants · Phase 2

    Cabozantinib in Patients With RET Fusion-Positive Advanced Non-Small Cell Lung Cancer and Those With Other Genotypes: ROS1 or NTRK Fusions or Increased MET or AXL Activity

  • NCT03519269 · 86 participants · NA

    Navio Robotic Versus Conventional Total Knee Arthroplasty

  • NCT04132999 · 86 participants · NA

    PAP for Children With DS and OSAS

  • NCT04545957 · 86 participants · NA

    Jump: MR Simulation For Radiation Therapy Master Protocol

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02069873, the US trial registry maintained by the National Library of Medicine. NCT02069873 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.