Trauma-Informed Intervention for Justice-Involved Men Facing Partner Violence
SAH
+ TAU
Trauma and Stressor Related Disorders+6
+ Affective Symptoms
+ Alcohol Drinking
Treatment Study
Summary
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.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.800 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.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
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
Active ComparatorStudy 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
CABU School of Medicine, Psychiatry
Boston, United StatesOpen CABU School of Medicine, Psychiatry in Google MapsRhode Island Hospital
Providence, United States