Enrolling by invitation

Trauma-Informed Intervention for Justice-Involved Men Facing Partner Violence

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being tested

SAH

+ TAU

Behavioral
Who is being recruted

Trauma and Stressor Related Disorders+6

+ Affective Symptoms

+ Alcohol Drinking

Over 18 Years
+2 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Interventional
Study Start: February 2025
See protocol details

Summary

Principal SponsorBoston University
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: February 13, 2025

Actual date on which the first participant was enrolled.

This study is focused on evaluating a program called Strength at Home (SAH) to help men who have been involved with the justice system manage issues related to partner violence. The program aims to reduce instances of both physical and psychological partner violence and address associated challenges such as posttraumatic stress disorder (PTSD) symptoms, difficulties in expressing emotions (known as alexithymia), and problems with alcohol use. The study targets 200 men, comparing those who participate in the SAH program with those who receive the usual treatment. By understanding how effective SAH is in reducing these problems, the study hopes to improve the support available for men dealing with these issues and ultimately enhance their well-being and relationships. Participants in the study will be randomly assigned to either the SAH program or the usual treatment group. They will undergo assessments before and after the treatment, with follow-ups every three months for a year. These assessments will track changes in partner violence, PTSD symptoms, emotional expression issues, and alcohol use. The study will also gather feedback from participants to assess their satisfaction with the treatment. By comparing results from both groups, the study aims to determine which approach is more effective. Additionally, the study will work with community advisors to identify any challenges in implementing the SAH program more broadly and to gather feedback from the community to refine the program further.

Official TitleA Randomized Controlled Trial to Evaluate a Trauma-Informed Partner Violence Intervention Program
NCT06803043
Principal SponsorBoston University
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

800 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Male

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Trauma and Stressor Related DisordersAffective SymptomsAlcohol DrinkingBehaviorMental DisordersBehavioral SymptomsDrinking BehaviorStress Disorders, Post-TraumaticStress Disorders, Traumatic

Criteria

1 inclusion criteria required to participate
Men court-mandated to IPV intervention from the Rhode Island Department of Parole and Probation and their partners

1 exclusion criteria prevent from participating
None

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
SAH isa trauma-informed 12-week intimate partner violence (IPV) intervention program.

Group II

Active Comparator
TAU is a 20-week state-approved IPV intervention program.

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 2 locations

Suspended

CABU School of Medicine, Psychiatry

Boston, United StatesOpen CABU School of Medicine, Psychiatry in Google Maps
Suspended

Rhode Island Hospital

Providence, United States
Enrolling by invitation2 Study Centers