NCT01435512

Brief Summary

This is a research study funded by the Department of Defense to test a therapeutic intervention for male combat veterans who engage in intimate partner violence (IPV). The investigators hope to decrease the recurrence of relationship aggression and help veterans manage anger. The primary aim of the study is to test the intervention.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
135

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Mar 2009

Longer than P75 for not_applicable

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 1, 2009

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

August 6, 2009

Completed
2.1 years until next milestone

First Posted

Study publicly available on registry

September 16, 2011

Completed
3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2014

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2014

Completed
6 years until next milestone

Results Posted

Study results publicly available

September 16, 2020

Completed
Last Updated

September 16, 2020

Status Verified

August 1, 2020

Enrollment Period

5.5 years

First QC Date

August 6, 2009

Results QC Date

July 14, 2017

Last Update Submit

August 27, 2020

Conditions

Keywords

PTSDCBTIntimate Partner ViolenceTreatment

Outcome Measures

Primary Outcomes (1)

  • Intimate Partner Aggression as Measured by the Conflict Tactics Scale

    Revised Conflict Tactics Scale-2 (CTS2). The CTS2 is the most widely used measure of IPV, with excellent internal consistency reliability, content validity, and construct validity.76,88 Combined partner reports will be used such that scores of partners who report a greater frequency of specific CTS2 behaviors will be used in analyses to reduce the impact of response biases and the underreporting of abuse. The CTS2 will also be given every four weeks during the course of active intervention. Scale response options range from 0 to 7. Higher overall scores mean more conflict.

    Pretreatment (baseline), Posttreatment (12 weeks), 3 month follow up (24 weeks)

Secondary Outcomes (4)

  • Multidimensional Measure of Emotional Abuse (MMEA)

    Pretreatment (baseline), Posttreatment (12 weeks), 3 month follow up (24 weeks)

  • Symptoms of Posttraumatic Stress Disorder as Assessed by the Clinician Administered PTSD Scale (CAPS) and the Posttraumatic Stress Disorder Checklist (PCL)

    6 month follow-up (72 weeks)

  • Relationship Satisfaction as Measured by the Dyadic Adjustment Scale

    6-month follow up (72 weeks)

  • Trait Anger as Measured by the State-Trait Anger Expression Inventory (STAXI) and Aggression as Measured by the Aggression Questionnaire

    6-month follow up (72 weeks)

Study Arms (2)

Group

EXPERIMENTAL

PTSD-Focused Cognitive Behavioral Therapy for Partner Violence

Behavioral: PTSD-Focused CBT for Partner Violence

Waitlist

NO INTERVENTION

Control group - no intervention

Interventions

PTSD-Focused CBT (PFCBT) will consist of 12 2-hour weekly sessions,led by two project therapists. In each session, group members will discuss materials and do assignments to practice skills.

Also known as: Strength at Home, Veterans Program
Group

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Any era veteran
  • Over the age of 18
  • In a relationship within a female partner within the last 6 months
  • At least one act of male-to-female physical aggression over the previous 6 months or at least one act of male-to-female severe violence in the past 12 months
  • Male participant must consent for partner contact

You may not qualify if:

  • Participant evidences severe organicity or active psychosis
  • Reading difficulties prevent valid completion of the assessment instruments
  • Participant expresses prominent suicidal or homicidal ideation
  • Participant meets diagnostic criteria for alcohol and/or drug dependence, if not in early full remission or sustained partial remission

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

National Center for PTSD/VA Boston Healthcare System

Boston, Massachusetts, 02130, United States

Location

Providence VA Medical Center

Providence, Rhode Island, 02908, United States

Location

Related Publications (2)

  • Taft CT, Macdonald A, Creech SK, Monson CM, Murphy CM. A Randomized Controlled Clinical Trial of the Strength at Home Men's Program for Partner Violence in Military Veterans. J Clin Psychiatry. 2016 Sep;77(9):1168-1175. doi: 10.4088/JCP.15m10020.

  • Creech SK, Macdonald A, Benzer JK, Poole GM, Murphy CM, Taft CT. PTSD symptoms predict outcome in trauma-informed treatment of intimate partner aggression. J Consult Clin Psychol. 2017 Oct;85(10):966-974. doi: 10.1037/ccp0000228. Epub 2017 Jul 20.

Related Links

MeSH Terms

Conditions

Stress Disorders, Post-Traumatic

Condition Hierarchy (Ancestors)

Stress Disorders, TraumaticTrauma and Stressor Related DisordersMental Disorders

Results Point of Contact

Title
Dr. Casey Taft
Organization
BVARI

Study Officials

  • Casey T. Taft, PhD

    VA Boston Healthcare System

    PRINCIPAL INVESTIGATOR
  • Suzannah Creech, PhD

    VA VISN 17 Center of Excellence

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
No
Restrictive Agreement
No

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

August 6, 2009

First Posted

September 16, 2011

Study Start

March 1, 2009

Primary Completion

September 1, 2014

Study Completion

September 1, 2014

Last Updated

September 16, 2020

Results First Posted

September 16, 2020

Record last verified: 2020-08

Locations