Completed

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

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What is being tested

Male-focused group violence prevention intervention

Behavioral
Who is being recruted

Behavior

+ Sexual Behavior

+ Coitus

Over 15 Years
+5 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Prevention Study

Interventional
Study Start: September 2008
See protocol details

Summary

Principal SponsorLondon School of Hygiene and Tropical Medicine
Last updated: March 4, 2013
Sourced from a government-validated database.Claim as a partner

Study start date: September 1, 2008

Actual date on which the first participant was enrolled.

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.

NCT01803932
Principal SponsorLondon School of Hygiene and Tropical Medicine
Last updated: March 4, 2013
Sourced from a government-validated database.Claim as a partner

Protocol

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

601 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Prevention Study

Prevention studies aim to stop a disease from developing. They often involve people at risk and test things like vaccines, lifestyle changes, or preventive medications.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 15 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

BehaviorSexual BehaviorCoitus

Criteria

4 inclusion criteria required to participate
15+ years old
capable of completing face-to-face interview independently and without causing undue psychological distress
females: female intimate partner of males in intervention or selected as control
males: participant in group intervention or selected as control
1 exclusion criteria prevent from participating
lack of informed consent

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Male-focused group violence prevention intervention

Group II

No Intervention
Communities in which male-focused group prevention activities will not be conducted

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

International Rescue Committee

Abidjan, Côte d’IvoireOpen International Rescue Committee in Google Maps
CompletedOne Study Center