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Purpose

The goal of this clinical trial is to test an abbreviated, intensive, multi-couple group version of cognitive-behavioral conjoint therapy for PTSD (AIM-CBCT for PTSD) in an active military and veteran population. The main questions it aims to answer are: - Does AIM-CBCT for PTSD improve PTSD symptoms? - Does AIM-CBCT for PTSD improve associated symptoms (e.g., depression), romantic partner distress, and couple relationship satisfaction? Participants will participate in a two-day retreat in which they are taught and practice skills to decrease PTSD symptoms and enhance their relationships. Researchers will compare AIM-CBCT for PTSD to the Prevention and Relationship Education Program (PREP) to determine whether it is superior to an evidence-based relationship education curriculum that is also delivered in a two-day multi-couple group format.

Condition

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Service member or veteran and a romantic partner willing to participate. - Couple is married or cohabiting for at least 3 months. Couple can be either different or same sex. - Service member/veteran diagnosis of PTSD as determined by the CAPS-5. - Each partner is at least 18 years old. - Both partners able to speak and read English.

Exclusion Criteria

  • Either partner reports current suicidal ideation severe enough to warrant immediate attention - Current homicide risk meriting crisis intervention for either partner - Current and severe alcohol misuse in either partner in the past 12 weeks and/or warranting immediate intervention - Recent (past month) manic episode or psychotic disorder symptoms in either partner - Evidence of a moderate or severe traumatic brain injury or other cognitive impairment in either partner - Couple is separated or have taken steps to dissolve their relationship - Either partner is currently participating in evidence-based treatment for PTSD (e.g., Prolonged Exposure, Cognitive Processing Therapy, Present-Centered Therapy for PTSD, Eye Movement Desensitization and Reprocessing, Cognitive-Behavioral Conjoint Therapy for PTSD, or Structured Approach Therapy). - Evidence or admission of severe intimate aggression as indicated by a "yes" endorsement to the one-question Screen for Conflict Question by either partner occurring within the past 6-months.

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Intervention Model Description
Randomized controlled trial with parallel group design
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)
Masking Description
Independent evaluators will be blinded as to participant treatment condition during follow-up assessments.

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Abbreviated, Intensive, Multi-Couple Group Cognitive-Behavioral Conjoint Therapy for PTSD 		AIM-CBCT for PTSD is an abbreviated, intensive, multi-couple group version of cognitive-behavioral conjoint therapy for PTSD, an evidence-based treatment for PTSD delivered in a conjoint format.
  • Behavioral: Abbreviated, Intensive, Multi-Couple Group Cognitive-Behavioral Conjoint Therapy for PTSD
    Approximately 12 hours of programming delivered over 2 consecutive days in a multi-couple group retreat format. Couples are provided with psychoeducation about PTSD and relationship functioning and are taught cognitive and behavioral skills to address the manifestation of PTSD in the couple relationship. Couples will also meet once individually with one of the group leaders 1-2 weeks before the retreat and once 1-2 weeks after the retreat.
Active Comparator
Prevention and Relationship Education Program 		PREP is an evidence-based relationship education program delivered in a multi-couple group format.
  • Behavioral: Prevention and Relationship Education Program
    Approximately 12 hours of programming delivered over 2 consecutive days in a multi-couple group retreat format.The content of PREP and workshop experiences focuses on helping couples communicate effectively, manage conflict without harming their relationship, preserve and act on commitment, improve relationship decision-making, increase understanding of differences between partners, and protect positive connections between partners. Approximately 12 hours of PREP content will be delivered over 2 consecutive days in a multi-couple group retreat format. Couples will also meet once individually with one of the group leaders 1-2 weeks before the retreat and will check in with a member of the study staff 1-2 weeks after the retreat.

Recruiting Locations

University of Texas Health Science Center at San Antonio
San Antonio, Texas 78229
Contact:
Alan Peterson, Ph.D.
210-562-6703
petersona3@uthscsa.edu

More Details

Status
Recruiting
Sponsor
Penn State University

Study Contact

Steffany J Fredman, Ph.D.
781-879-9758
sjf23@psu.edu

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.