Intervention Program With Perpetrators of Intimate Partner Violence

October 31, 2022 updated by: Olga Cunha, University of Minho
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.

Study Overview

Status

Recruiting

Intervention / Treatment

Study Type

Interventional

Enrollment (Anticipated)

50

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Póvoa De Varzim, Portugal
        • Recruiting
        • Junta de Freguesia Aver-o-Mar
        • Contact:
    • None Selected
      • Braga, None Selected, Portugal, 4704-553
        • Recruiting
        • Associação de Psicologia da Universidade do Minho
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 70 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

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.

Exclusion Criteria:

  • psychotic disorders;
  • cognitive impairment;
  • psychological and/or personality disorders;
  • substance abuse.

Study Plan

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

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: NON_RANDOMIZED
  • Interventional Model: PARALLEL

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: 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.
EXPERIMENTAL: 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.
NO_INTERVENTION: 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).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Perpetration of abuse against intimate partner
Time Frame: 18 weeks
Marital Violence Inventory (IVC) - Total scores range between 0 and 40. Higher scores mean a higher frequency of intimate partner violence.
18 weeks
Attitudes towards intimate partner violence
Time Frame: 18 weeks
Attitudes towards Marital Violence Scale (ECVC) - Total score ranges between 25 and 125. Higher scores mean more supportive attitudes towards intimate partner violence.
18 weeks
Psychopathological symptoms
Time Frame: 18 weeks
Bref Symptom Inventory (BSI) - BSI includes nine dimensions and three global indexes. Higher scores mean more psychopathological symptoms.
18 weeks
Coping skills
Time Frame: 18 weeks
Coping scale - Total score ranges between 13 and 52. Higher scores mean better coping skills.
18 weeks
Risk of intimate partner violence
Time Frame: 18 weeks
Spouse Abuse Risk Assessment (SARA) - Total scores range between 0 and 40. Higher scores mean a higher risk of intimate partner violence.
18 weeks
Motivation to change
Time Frame: 18 weeks
University Rhode Island Change Assessment - Domestic Violence - Revised (URICA-DV-R) - URICA-DV-R includes a Readiness to Change Index - higher scores mean higher readiness to change.
18 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Self-esteem
Time Frame: 18 weeks
Rosenberg Self-esteem scale (RSES) - Total scores range between 10 and 40. Higher scores mean higher self-esteem.
18 weeks
Self-concept
Time Frame: 18 weeks
Self-concept inventory (ICAC) - Total scores range between 20 and 100. Higher scores mean higher self-concept.
18 weeks
Aggression
Time Frame: 18 weeks
Buss-Perry Aggression Questionnaire (BPAQ) - Total scores range between 29 and 145. Higher scores mean higher levels of aggression.
18 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

January 1, 2010

Primary Completion (ACTUAL)

September 1, 2022

Study Completion (ANTICIPATED)

December 1, 2025

Study Registration Dates

First Submitted

June 21, 2022

First Submitted That Met QC Criteria

August 1, 2022

First Posted (ACTUAL)

August 2, 2022

Study Record Updates

Last Update Posted (ACTUAL)

November 1, 2022

Last Update Submitted That Met QC Criteria

October 31, 2022

Last Verified

October 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • CE.CSH 102/2018

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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