- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05484440
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
Conditions
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:
- Paula Coelho
- Email: pamcds@gmail.com
-
-
None Selected
-
Braga, None Selected, Portugal, 4704-553
- Recruiting
- Associação de Psicologia da Universidade do Minho
-
Contact:
- Rui Abrunhosa Gonçalves, Phd
- Email: rabrunhosa@psi.uminho.pt
-
-
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.
Sponsor
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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