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NCT01803932 Clinical Trial

Evaluation of a Male-focused Intervention to Prevent Intimate Partner Violence in a Conflict-affected Setting

Domestic Violence Clinical Trial

Official title:
Evaluation of a Male-focused Primary Prevention Intervention to Prevent Intimate Partner Violence in a Conflict-affected Setting: A Cluster Randomized Controlled Trial in Cote d'Ivoire

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01803932
Other study ID # InterveneDV-CI
Secondary ID
Status Completed
Phase N/A
First received February 25, 2013
Last updated March 1, 2013
Start date September 2008
Est. completion date March 2012

Study information
Verified date March 2013
Source London School of Hygiene and Tropical Medicine
Contact n/a
Is FDA regulated No
Health authority UK: LSHTM Ethics Committee
Study type Interventional

Clinical Trial Summary

Cluster randomized controlled trial to evaluate a male-focused primary prevention programme which used a men's only group discussion format to prevent intimate partner violence against women & girls through fostering knowledge and behaviour changes by: (1) increasing men's knowledge on the impact of violence against women; (2) promoting gender equitable beliefs/behaviours within relationships; and (3) developing anger management techniques.

Recruitment information / eligibility
Status Completed
Enrollment 601
Est. completion date March 2012
Est. primary completion date November 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 15 Years and older
Eligibility Inclusion Criteria:

- 15+ years old

- males: participant in group intervention or selected as control

- females: female intimate partner of males in intervention or selected as control

- capable of completing face-to-face interview independently and without causing undue psychological distress

Exclusion Criteria:

- lack of informed consent

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Intervention

Behavioral:
• Male-focused group violence prevention intervention

Locations
Country Name City State
Côte D'Ivoire International Rescue Committee Abidjan

Sponsors (2)
Lead Sponsor Collaborator
London School of Hygiene and Tropical Medicine International Rescue Committee

Country where clinical trial is conducted

Côte D'Ivoire, 

Outcome
Type Measure Description Time frame Safety issue
Primary Past 12 months victimisation/perpetration of physical or sexual intimate partner violence 1 year after intervention completion No
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