- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02153554
Impact Evaluation of Training Civil Servants on Violence Against Women in Medellín, Colombia
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"
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Bogota, Colombia
- Econometria Consultores
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Women who initiate and finalize the process with the comissaries of family
Study Plan
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
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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.
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Average of 8 months after the complaint was presented at the comissaries
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Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
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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