Impact Evaluation of Training Civil Servants on Violence Against Women in Medellín, Colombia

February 6, 2017 updated by: Econometría Consultores

Capacity of State and Local Actors to Respond to Violence Against Women: Impact Evaluation of Training Civil Servants on Violence Against Women in Medellín (Colombia), Component of the Program "Seguridad Pública"

The purpose of this study is to determine whether the training of civil servants leads to a reduction in the violence suffered by women, as well as in their psychological wellbeing and attitudes towards violence.

Study Overview

Detailed Description

The Secretary of Women of Medellin, through the ICONTEC, intends to conduct training to officials of the 22 family commissioners in Medellin. The objective of these trainings is to standardize procedures in order that women do not feel re-victimized and can forward complaints. Since the training will be done in phases in 2014 and there is willingness of relevant stakeholders to generate a random order on which commissioners the training is first performed, it can be done a cluster randomized trial.

We will require all 22 commissioners to be randomly assigned into two groups, one treatment and one control. To implement it is intended to:

  • Conduct a baseline survey amongst women who used the services of the commissionaires between June and Septmber 2013, completed the process of care and signed informed consent.
  • Training of a randomly chosen set of 11 commissioners will take place between June and September 2014.
  • Conduct an endline survey amongst women who used the services of any of the 22 commissionaires between June and September 2014, completed the process of care and signed informed consent.

Women will be contacted through the commissioners. Women who have completed the process of care will be ask whether they want to participate in the study. If they agree, their contact details will transfer to the investigators for the survey to be conducted. This process would be conducted twice for baseline information before beginning the training, and for endline, once half of the first 11 commissioners have been trained.

Study Type

Interventional

Enrollment (Actual)

975

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

      • Bogota, Colombia
        • Econometria Consultores

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 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • Women who initiate and finalize the process with the comissaries of family

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: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Trained
Training civil servants in Medellin (Colombia) on attention to violence against women.
The Secretary of Women of Medellin, through the ICONTEC, intends to conduct training to officials of the 22 family commissioners in Medellin. The objective of these trainings is to standardize procedures in order that women do not feel re-victimized and can forward complaints.
No Intervention: Non trained

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Occurrence of violence
Time Frame: 3 months
The outcome will be measure through a survey to women who used the services of the commissionaires, completed the process of care and signed informed consent
3 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Knowledge, attitudes and practices (KAP) on violence and care pathways
Time Frame: Average of 8 months after the complaint was presented at the comissaries
The outcome will be measure through a survey to women who used the services of the commissionaires, completed the process of care and signed informed consent
Average of 8 months after the complaint was presented at the comissaries
Psychological well-being (self-acceptance, positive relationships, autonomy, environmental mastery, personal growth, purpose in life)
Time Frame: Average of 8 months after the complaint was presented at the comissaries
The outcome will be measure through a survey to women who used the services of the commissionaires, completed the process of care and signed informed consent
Average of 8 months after the complaint was presented at the comissaries
Time resolution of cases
Time Frame: Average of 8 months after the complaint was presented at the comissaries
The outcome will be measured through secondary data of the commissaries with information between the time of the initiation of the complaint and the completed the process of care.
Average of 8 months after the complaint was presented at the comissaries

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

May 1, 2014

Primary Completion (Actual)

November 1, 2015

Study Completion (Actual)

June 1, 2016

Study Registration Dates

First Submitted

May 28, 2014

First Submitted That Met QC Criteria

June 2, 2014

First Posted (Estimate)

June 3, 2014

Study Record Updates

Last Update Posted (Estimate)

February 7, 2017

Last Update Submitted That Met QC Criteria

February 6, 2017

Last Verified

February 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • ATN/MG-13064-RG ECO 577-3

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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