RECRUITING

Family Involvement in Treatment for PTSD (FIT-PTSD): A Brief, Feasible Method for Enhancing Outcomes, Retention, and Engagement

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

Although effective treatments for PTSD exist, high rates of treatment dropout and sub-optimal response rates remain common. Incorporating family members in treatment represents one avenue for improving outcomes and providing Veteran-centered care, and surveys of Veterans in outpatient VA PTSD care indicate that 80% desire family involvement. The VA has invested many years and millions of dollars on the dissemination of Cognitive Processing Therapy (CPT) and Prolonged Exposure (PE) for PTSD. A family-based intervention that complements these two first-line treatments would capitalize on existing treatment infrastructure while also potentially boosting outcomes and retention. Preliminary testing of the proposed Brief Family Intervention (BFI) resulted in 50% less dropout from CPT/PE among Veterans whose family members received the BFI. There was also a large impact on PTSD symptoms at 16 weeks (d = 1.12) in favor of the BFI group. The goal of this study is to test the effectiveness of the BFI among a fully-powered sample. One hundred Veteran-family member dyads (n = 200) will be recruited. Veterans will be beginning a course of usual-care CPT or PE at one of two VA sites. Family members will be randomized to receive or not receive the BFI, a two-session psychoeducational and skills-based protocol. PTSD symptom severity and treatment retention will be the primary outcomes. Assessments will be conducted by independent evaluators at baseline, 6-, 12-, 18-, and 26-weeks. Veterans whose family members receive the BFI are expected to have lower dropout and a greater rate of change in their PTSD symptoms compared to Veterans whose family members do not receive the BFI. If the BFI is found to increase the effectiveness of and retention in CPT/PE, it will be a highly appealing option for incorporating families into Veterans' PTSD care.

Official Title

Family Involvement in Treatment for PTSD (FIT-PTSD): A Brief, Feasible Method for Enhancing Outcomes, Retention, and Engagement

Quick Facts

Study Start:2022-07-01
Study Completion:2026-03-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05267665

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. * a current DSM-5 diagnosis of PTSD
  2. * Veteran status
  3. * willing to have a family member involved in the study
  4. * has recently begun or is currently initiating individual CPT or PE (completed no more than 3 sessions of the protocol at the time of the baseline assessment)
  5. * If taking psychotropic medication, the Veteran must be on a stable dose for at least 30 days.
  6. * age 18 or older, family member of the Veteran (significant other, parent, adult child, sibling, etc.)
  7. * currently having frequent contact with the Veteran (three or more times per week)
  1. * current engagement in couple/family treatment with the identified family member participant
  2. * current severe substance use disorder (mild/moderate use disorders will not be excluded)
  3. * current psychosis or unstable bipolar disorder diagnosis
  4. * high suicidal risk
  5. * significant cognitive impairment
  6. * same as listed for Veterans. Additionally
  7. * family members will NOT be permitted to participate if they meet criteria for current PTSD

Contacts and Locations

Study Contact

Johanna Thompson-Hollands, PhD
CONTACT
(857) 364-2067
Johanna.Thompson-Hollands@va.gov
Cameron Busser, BA
CONTACT
(857) 364-4143
cameron.busser@va.gov

Principal Investigator

Johanna Thompson-Hollands, PhD
PRINCIPAL_INVESTIGATOR
VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA

Study Locations (Sites)

VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA
Boston, Massachusetts, 02130-4817
United States
Durham VA Medical Center, Durham, NC
Durham, North Carolina, 27705-3875
United States
Cincinnati VA Medical Center, Cincinnati, OH
Cincinnati, Ohio, 45220
United States

Collaborators and Investigators

Sponsor: VA Office of Research and Development

  • Johanna Thompson-Hollands, PhD, PRINCIPAL_INVESTIGATOR, VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA

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 Date2022-07-01
Study Completion Date2026-03-01

Study Record Updates

Study Start Date2022-07-01
Study Completion Date2026-03-01

Terms related to this study

Keywords Provided by Researchers

  • Posttraumatic stress disorder
  • PTSD
  • Veteran
  • Family treatment

Additional Relevant MeSH Terms

  • Posttraumatic Stress Disorder