Partner Violence and Anger Management
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ClinicalTrials.gov Identifier: NCT01653860 |
Recruitment Status :
Completed
First Posted : July 31, 2012
Last Update Posted : November 3, 2020
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The purpose of this study is to investigate the effectiveness of the Brøset anger management model in reducing violent behavior amongst clients who are violent in intimate partnerships and who voluntarily seek help.
Violence in intimate partnerships constitutes a serious problem worldwide and there is reason to believe that cognitive behavior therapy has some effect on the reduction of violent behavior. However, there are currently too few randomized controlled studies to conclude about the effectiveness of cognitive behavior therapy for this client group.
Condition or disease | Intervention/treatment | Phase |
---|---|---|
Domestic Violence Spouse Abuse | Behavioral: The Brøset anger management model Behavioral: Ordinary group treatment | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 185 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Prevention |
Official Title: | Partner Violence and Anger Management: a Randomised Controlled Study of the Effectiveness of Cognitive Behavioral Therapy |
Actual Study Start Date : | July 2012 |
Actual Primary Completion Date : | May 4, 2018 |
Actual Study Completion Date : | May 4, 2018 |
Arm | Intervention/treatment |
---|---|
Experimental: The Brøset anger management model
Group treatment
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Behavioral: The Brøset anger management model
manualised structured cognitive treatment program 15 weeks (30 hours) |
Active Comparator: ordinary group treatment
Group treatment
|
Behavioral: Ordinary group treatment
group treatment 8 weeks (16 hours) |
- violent behaviour, reported by partner and client [ Time Frame: 3 months between assessments, 1 year duration, i.e. baseline and 4 follow-up assessments. In accordance with the original Norwegian protocol. ]measured by using the Conflict Tactics Scale Revised (CTS2), instrument for measuring violence in intimate partnerships(10), which consists of 78 questions (0-7) about different aspects of violence (frequence of physical, psychological, sexual and material violence)
- The client's and their partner's mental health [ Time Frame: 3 months between assessments, 1 year duration, i.e. baseline and 4 follow-up assessments. In accordance with the original Norwegian protocol. ]measured by using the Hopkins Symptoms Check List (HSCL-25, with 25 questions about the presence and intensity of anxiety and depression symptoms, and symptoms of somatoform character)
- The client's and their partner's health service use and absence due to sickness [ Time Frame: 3 months between assessments, 1 year duration, i.e. baseline and 4 follow-up assessments. In accordance with the original Norwegian protocol. ]
- Changes in emotional dysregulation [ Time Frame: 3 months between assessments, 1 year duration, i.e. baseline and 4 follow-up assessments. In accordance with the original Norwegian protocol. ]Emotional regulation will be assessed by the Difficulties in Emotion Regulation Scale (DERS, Gratz & Roemer, 2004).

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | Male |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- fluent in Norwegian language
- is in a partner relationship at inclusion. Partner relationship is defined by having an intimate partner at present, or being in regular contact with a former intimate partner so that violence is possible (e.g. they have children)
- admits being violent to his partner (physical, mental and/or sexual)
Exclusion Criteria:
- psychosis
- alcohol- or drug addiction to a level that hinders group participation free from intoxication.

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01653860
Norway | |
St Olavs University Hospital, Division of Psychiatry, Centre for research and education in forensic psychiatry Brøset | |
Trondheim, Norway, 7440 |
Principal Investigator: | Tom Palmstierna, MD PhD prof | Norwegian University of Science and Technology |
Responsible Party: | Norwegian University of Science and Technology |
ClinicalTrials.gov Identifier: | NCT01653860 |
Other Study ID Numbers: |
2012/683 |
First Posted: | July 31, 2012 Key Record Dates |
Last Update Posted: | November 3, 2020 |
Last Verified: | November 2020 |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
Behavior therapy Group therapy |