Intervention Program With Perpetrators of Intimate Partner Violence

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2010-01-31

Study Completion Date

2025-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The current project aims to develop, implement and assess the effectiveness of an intervention program for perpetrators of intimate partner violence (both volunteers and court-mandated) that incorporates Motivational Interviewing techniques (MIT) as well as cognitive-behavioral and psychoeducational strategies implemented in a community setting. The intervention focuses on ending violence against the intimate partner and promoting the batterer's personal and social skills. The study uses pre- and post-treatment measures, with an experimental group (intervention) and two control groups (a group without intervention and a group without MIT). Data were collected at pre-test, post-test, and follow-up.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Motivational Interviewing Intervention for Intimate Partner Violence

NCT01410669

Self-efficacy

COMPLETED NA

Intervention for Men Who Batter Women

NCT02722317

Violence

COMPLETED

A Randomized Clinical Study of a Mind-Body Approach to Domestic Violence Offender Treatment

NCT00983593

Domestic Violence Intimate Partner Violence

COMPLETED NA

The IPV Provider Network: Engaging the Health Care Provider Response to Interpersonal Violence Against Women

NCT03259646

Violence, Domestic Violence, Sexual

COMPLETED NA

Evaluating the Efficacy of a New Sexual Violence Prevention Program with College Students

NCT06887361

Sexual Violence

RECRUITING NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Intimate Partner Violence

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Group cognitive-behavioral intervention plus individual Motivational Interviewing

Group participants will participate in six individual sessions based on Motivational Interviewing techniques (60 minutes each) and then in 18 group sessions based on psychoeducational and cognitive-behavioral techniques (90 to 120 minutes each). Groups will be composed of 6 to 10 participants. The intervention will be delivered weekly.

Group Type EXPERIMENTAL

Psychological

Intervention Type OTHER

Group cognitive-behavioral intervention

Group participants will participate in 18 group sessions based on psychoeducational and cognitive-behavioral techniques (90 to 120 minutes each). Groups will be composed of 6 to 10 participants. The intervention will be delivered weekly.

Group Type EXPERIMENTAL

Psychological

Intervention Type OTHER

Treatment as usual (TAU)

Group participants will receive the usual treatment delivered by different institutions (e.g., correctional services, probation services, child protection services) as the participants of this study are justice-involved individuals (i.e., perpetrators of intimate partner violence).

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Psychological

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* being an adult male;
* having perpetrated physical, psychological, and/or sexual violence against a female intimate partner or ex-partner;
* be able to read and write.