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Completed Not applicable Interventional

Testing the Effectiveness of a Therapist-Assisted Self-Management Program for Veterans Who Finished PTSD Therapy

ClinicalTrials.gov ID: NCT05797441

Public ClinicalTrials.gov record NCT05797441. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 1:37 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Empowering Veterans to Self-Manage PTSD Symptoms Following Completion of Trauma-Focused Therapy

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Patients who complete prolonged exposure and cognitive processing therapy, the treatments for posttraumatic stress disorder (PTSD) with the most empirical support, continue to express a need for mental health treatment. A therapist-assisted self-management program for patients who have completed one of these two treatments and achieved symptom improvement has the potential to meet patients' stated treatment needs, maintain or build upon their PTSD symptom reductions, increase their confidence in managing their symptoms, and reduce the number of mental health appointments that they need to attend. Further, reducing the number if mental health sessions attended by completers of these time and resource intensive psychotherapies will increase the likelihood that their implementation in regular-practice clinics will be maintained.

Study identification

NCT ID
NCT05797441
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Enrollment
80 participants

Conditions and interventions

Interventions

Behavioral · Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 16, 2023 (Actual)
Primary completion
Mar 23, 2026 (Actual)
Completion
Mar 23, 2026 (Actual)
Last update posted
Apr 8, 2026

2023 – 2026

United States locations

U.S. sites
8
U.S. states
7
U.S. cities
8
Facility City State ZIP Site status
VA Greater Los Angeles Healthcare System, Sepulveda, CA Sepulveda California 91343 —
James A. Haley Veterans' Hospital, Tampa, FL Tampa Florida 33612 —
Jesse Brown VA Medical Center, Chicago, IL Chicago Illinois 60612 —
Edward Hines Jr. VA Hospital, Hines, IL Hines Illinois 60141-3030 —
Minneapolis VA Health Care System, Minneapolis, MN Minneapolis Minnesota 55417-2309 —
Durham VA Medical Center, Durham, NC Durham North Carolina 27705-3875 —
Cincinnati VA Medical Center, Cincinnati, OH Cincinnati Ohio 45220-2213 —
Wm. Jennings Bryan Dorn VA Medical Center, Columbia, SC Columbia South Carolina 29209-1638 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05797441, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 8, 2026 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05797441 live on ClinicalTrials.gov.

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