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NCT02290639 · ClinicalTrials.gov registry record · NA

Brief Cognitive Behavioral Treatment of Deployment-Related PTSD Symptoms in Primary Care Settings

A NA study of Post Traumatic Stress Disorder, sponsored by The University of Texas Health Science Center at San Antonio.

Completed
Registry status
NA
Development phase
74
Enrollment target
2
Study locations

NCT02290639: Completed NA study of Post Traumatic Stress Disorder, sponsored by The University of Texas Health Science Center at San Antonio.

NCT02290639 is a NA study of Post Traumatic Stress Disorder that has completed, run by The University of Texas Health Science Center at San Antonio. The registered enrollment target is 74 participants, below the 664-participant average among 262 other Post Traumatic Stress Disorder trials with a reported enrollment target (89% lower). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02290639, a NA study of Post Traumatic Stress Disorder, has completed, sponsored by The University of Texas Health Science Center at San Antonio.

COMPLETED
Registry status
NA
Development phase
74 participants
Enrollment target
2
Study locations

Study Summary

A significant number of veterans of the wars in Iraq and Afghanistan are affected by posttraumatic stress disorder (PTSD). The limited reach of effective treatments for PTSD into the veteran population is at least partially due to the perceived stigma by service members for seeking help in traditional specialty mental health clinics. A comprehensive approach to PTSD treatment in a veteran population should provide alternative sources for accessing effective psychotherapy treatments. The purpose of study is to conduct a randomized clinical trial comparing a brief (four 30-minute sessions delivered over 6 weeks) cognitive-behavioral therapy (CBT) protocol designed specifically for use by behavioral health consultants working in an integrated primary care setting to a minimal contact 6-week control. The primary outcome measure is PTSD symptom relief.

Primary Outcome

The PSS-I is a 20-minute, 17-item clinical interview that evaluates each of the DSM-IV PTSD symptoms during the past 2 weeks on a frequency/severity scale (Foa, Riggs, Dancu, \& Rothbaum, 1993). The PSS-I is comparable to the gold standard employed in studies of veterans (the Clinician Administered PTSD Scale; CAPS) yet takes considerably less time to administer (Foa \& Tolin, 2000). Each symptom is rated on a 4-point scale ranging from 0 (not at all) to 3 (very much). Subscale scores are calcul

Conditions Studied

Post Traumatic Stress Disorder

Interventions

  • BEHAVIORAL Brief Cognitive Behavioral Treatment
  • BEHAVIORAL Minimal Contact

Study Locations (2)

Texas

  • Wilford Hall Ambulatory Surgical Center Family Medicine Clinic - Lackland Air Force Base
  • Joint Base San Antonio - Randolph Air Force Base

Trial Details

FieldValue
Enrollment Target 74 participants
Start Date 2012-12
Est. Completion 2015-11
Phase NA
The University of Texas Health Science Center at San Antonio

378 total trials

What the finished NCT02290639 record still lists

NCT02290639 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 74 participants, a relatively small participant target, below the 664-participant average among 262 other Post Traumatic Stress Disorder trials with a reported enrollment target (89% lower).

The record links to 1 condition, with Post Traumatic Stress Disorder appearing as the primary indexed condition, and to 2 interventions - of which Brief Cognitive Behavioral Treatment is the first listed.

NCT02290639 reports a single indexed study location in Texas.

Frequently Asked Questions

What is clinical trial NCT02290639 about?

NCT02290639 is a clinical study titled "Brief Cognitive Behavioral Treatment of Deployment-Related PTSD Symptoms in Primary Care Settings". A significant number of veterans of the wars in Iraq and Afghanistan are affected by posttraumatic stress disorder (PTSD). The limited reach of effective treatments for PTSD into the veteran population is at least partially due to the perceived stigma by service members for seeking help in tradition...

What is the current status of trial NCT02290639?

This trial is currently completed. It is a NA study. The enrollment target is 74 participants. The study started on 2012-12. Estimated completion is 2015-11.

What conditions does trial NCT02290639 study?

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

What interventions are being tested in trial NCT02290639?

The interventions under investigation include: Brief Cognitive Behavioral Treatment (BEHAVIORAL), Minimal Contact (BEHAVIORAL).

Who is sponsoring clinical trial NCT02290639?

This trial is sponsored by The University of Texas Health Science Center at San Antonio, which has 378 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02290639 being conducted?

This trial has 2 study locations across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Learn More About Clinical Trials

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 NCT02290639's enrollment target sits among peer trials

74 148th of 262 higher than 115 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

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Related registry views

Source: ClinicalTrials.gov NCT02290639, the US trial registry maintained by the National Library of Medicine. NCT02290639 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.