RECRUITING

A Hybrid 1 Effectiveness-Implementation Trial of Partner-Assisted Prolonged Exposure for PTSD

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

PTSD occurs in up to 17% of post-9/11 US Service Members and is associated with long-term functional impairment, family problems, unemployment, and suicidality. Trauma-focused therapies (TFTs), such as Prolonged Exposure (PE), result in significant relief for many. Yet, TFTs are not equally effective for everyone. An important minority (\~40%) will retain their PTSD diagnoses after treatment, and many discontinue treatment prematurely, especially post-9/11 Service Members. TFTs are also more effective in addressing symptoms than psychosocial functioning. More work is needed to improve the consistency and potency of TFTs. Partnering with significant others may provide a powerful method for helping individuals get more out of their PTSD treatment. Observational research shows that relationship factors can help patients initiate, stay in, and experience greater benefit from PTSD treatment. Veterans that were surveyed experienced greater treatment gains when they shared more about their treatment with loved ones and when loved ones accommodated less for PTSD symptoms. Despite the promise of partner-involved interventions, there is no couples approach to PTSD treatment that has demonstrated superior outcomes to individual-only treatment models (i.e., TFTs). To address this gap, the investigators have completed a series of partner-assisted PTSD treatment studies, leading up the current proposal (Partnered PE, PPE). The investigators found that treatment completion rates were better than routine clinical care, and the treatment led to large improvements in participants' functioning, PTSD symptoms, and romantic functioning. For this proposed study, the primary objective is to conduct a randomized controlled trial (Research Level 3; larger-scale clinical trial) to test the superiority of PPE to standard PE among post 9/11 Veterans. The investigator's primary hypothesis is that PPE will lead to greater improvements in psychosocial functioning than standard PE. Secondary and tertiary aims examine posttreatment clinical outcomes (PTSD, depression) and intimate partner outcomes (relationship functioning, distress, caregiver burden, and psychosocial functioning), as well as examine strategies for PPE implementation. In exploratory aims, the investigators will examine the stability of group differences, treatment completion rates, the role military sexual trauma history, and treatment mechanisms.

Official Title

A Hybrid 1 Effectiveness-Implementation Trial of Partner-Assisted Prolonged Exposure for PTSD

Quick Facts

Study Start:2025-05-16
Study Completion:2028-08-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06990191

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Post-9/11 Veteran Enrolled in VHA
  2. * 1 \> mo stable medication
  3. * Committed relationship 6+ months
  4. * DSM-5-R PTSD Diagnosis
  1. * Imminent suicidality/homicidally
  2. * Mania, psychosis, or severe substance use disorder, past 3 mos
  3. * Severe cognitive impairment
  4. * Severe intimate partner violence in last 6 months
  5. * Fear of or intimidation by partner
  6. * Partner screens positive for PTSD

Contacts and Locations

Study Contact

Erin Linden
CONTACT
612-725-2000
erin.linden@va.gov
Donald Lemon
CONTACT
(612) 467-1957
donald.lemon2@va.gov

Principal Investigator

Laura Meis, PhD
PRINCIPAL_INVESTIGATOR
University of Minnesota, National Center for PTSD, Minneapolis VA Healthcare System
Leslie Morland, PhD
PRINCIPAL_INVESTIGATOR
National Center for PTSD; San Diego VA Healthcare System

Study Locations (Sites)

Phoenix VA Healthcare System
Phoenix, Arizona, 85012
United States
San Diego VA Healthcare System
San Diego, California, 92161
United States
Minneapolis VA Healthcare System
Minneapolis, Minnesota, 55417
United States
Charleston VA Healthcare System
Charleston, South Carolina, 29401
United States

Collaborators and Investigators

Sponsor: United States Department of Defense

  • Laura Meis, PhD, PRINCIPAL_INVESTIGATOR, University of Minnesota, National Center for PTSD, Minneapolis VA Healthcare System
  • Leslie Morland, PhD, PRINCIPAL_INVESTIGATOR, National Center for PTSD; San Diego VA Healthcare System

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-05-16
Study Completion Date2028-08-31

Study Record Updates

Study Start Date2025-05-16
Study Completion Date2028-08-31

Terms related to this study

Keywords Provided by Researchers

  • Trauma-focused therapies
  • Prolonged exposure
  • Veterans
  • Integrative Behavioral Couples Therapy
  • couples
  • PTSD

Additional Relevant MeSH Terms

  • Post Traumatic Stress Disorder