- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03210454
Evaluation of Marketing Interventions in Colombia
Evaluation Of The Effect Of Marketing Interventions For Women On Economic Empowerment And Risk Of Intimate Partner Violence In Colombia
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The proposed project seeks to implement a cluster-randomized controlled trial (RCT) to measure the impact of increasing women´s incomes and providing gender equality trainings on women´s empowerment and risk of intimate partner violence (IPV) in Colombia. This project will be the first in Latin America to evaluate rigorously the impact of a marketing intervention, alone and combined with IPV prevention training. The knowledge generated from this evaluation has the potential to identify the most effective solutions to empower women, as well as to drive transformative change in current approaches to reduce IPV and promote gender equality in highly vulnerable populations in Colombia, and worldwide.
The goal of the project is to estimate the impact of generating livelihood opportunities and providing gender-based violence (GBV) training to reduce IPV among women in Colombia. This will generate much needed evidence on the most effective approach to empower women smallholder farmers and reduce their exposure to IPV. Investigators will conduct a cluster randomized controlled trial targeting approximately 100 smallholder farmers' associations and approximately 2700 women. Results will inform and strengthen future programming of humanitarian assistance and can be replicated in humanitarian interventions in other parts of the world.
The experimental operational research will compare two programmatic modalities and their impact on women's risk of exposure to IPV, against a comparison group where no intervention takes place. The modalities will include: (1) providing a stable income for women, and (2) providing a stable income and IPV trainings to women. The evaluation will take place in five departments: Cauca, Valle de Cauca, Meta, Caquetá, and Nariño.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Bogotá
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Aurora, Bogotá, Colombia
- World Food Programme Colombia
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Women currently married or living together with a man as if married
- Males or females who are active within the farmer's association are eligible to participate
Exclusion Criteria:
- Women who have a husband/partner who is living elsewhere permanently
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Treatment Group 1
Farmers associations, including men and women, will be randomized to receive the smallholder marketing intervention.
|
The smallholder marketing intervention involves product purchasing (e.g., bananas, beans, goats, eggs) from smallholder farmers' associations through WFP's large procurement procedures.
WFP is will also provide technical training on topics such as sustainable farming practices, quality control, and business practices.
|
|
Experimental: Treatment Group 2
Farmers associations, including men and women, will be randomized to receive the smallholder marketing intervention combined with the intimate partner violence (IPV) prevention training.
|
The smallholder marketing intervention involves product purchasing (e.g., bananas, beans, goats, eggs) from smallholder farmers' associations through WFP's large procurement procedures.
WFP is will also provide technical training on topics such as sustainable farming practices, quality control, and business practices.
IPV prevention training involves 24 hours of gender training (gender equality and rights, economic empowerment, gender-based violence prevention), and 8 hours of nutrition and food security training (with a focus on gender).
|
|
No Intervention: Comparison Group 3
Women involved with farmers's associations that work independently of World Food Programmes (WFP's) assistance.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Incidence Physical and/or Sexual IPV
Time Frame: Post-Baseline (12 Months)
|
The number of new physical and/or sexual IPV encounters as reported in the study survey.
|
Post-Baseline (12 Months)
|
|
Change in Prevalence of Physical and/or Sexual IPV
Time Frame: Baseline, End-Line (12 Months Post Intervention)
|
The difference in the number of physical or sexual IPV encounters between baseline and post intervention as reported in the study survey.
|
Baseline, End-Line (12 Months Post Intervention)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Incidence Physical IPV
Time Frame: Post-Baseline (12 Months)
|
The number of new physical IPV encounters reported.
|
Post-Baseline (12 Months)
|
|
Incidence Sexual IPV
Time Frame: Post-Baseline (12 Months)
|
The number of new sexual IPV encounters as reported in the study survey.
|
Post-Baseline (12 Months)
|
|
Incidence Psychological IPV
Time Frame: Post-Baseline (12 Months)
|
The number of new physiological IPV encounters as reported in the study survey.
|
Post-Baseline (12 Months)
|
|
Incidence Economic Coercion
Time Frame: Post-Baseline (12 Months)
|
The number of new encounters of economic coercion as reported in the study survey.
|
Post-Baseline (12 Months)
|
|
Change in Prevalence of Physical IPV
Time Frame: Baseline, End-Line (12 Months Post Intervention)
|
The difference in the number of physical IPV encounters between baseline and post intervention as reported in the study survey.
|
Baseline, End-Line (12 Months Post Intervention)
|
|
Change in Prevalence of Sexual IPV
Time Frame: Baseline, End-Line (12 Months Post Intervention)
|
The difference in the number of sexual IPV encounters between baseline and post intervention as reported in the study survey.
|
Baseline, End-Line (12 Months Post Intervention)
|
|
Change in Prevalence of Psychological IPV
Time Frame: Baseline, End-Line (12 Months Post Intervention)
|
The difference in the number of psychological IPV encounters between baseline and post intervention as reported in the study survey.
|
Baseline, End-Line (12 Months Post Intervention)
|
|
Change in Prevalence of Economic Coercion
Time Frame: Baseline, End-Line (12 Months Post Intervention)
|
The difference in the number of economic coercion encounters between baseline and post intervention as reported in the study survey.
|
Baseline, End-Line (12 Months Post Intervention)
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Women's Attitudes Towards Gender
Time Frame: End-Line (12 Months Post Intervention)
|
General attitudes towards gender will be qualitatively collected via interview from women post intervention.
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End-Line (12 Months Post Intervention)
|
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Change in Women's Economic Empowerment
Time Frame: Baseline, End-Line (12 Months Post Intervention)
|
Changes in women's thoughts on economic empowerment will be qualitatively collected via interview.
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Baseline, End-Line (12 Months Post Intervention)
|
|
Change in Women's Attitudes Towards Gender
Time Frame: Baseline, End-Line (12 Months Post Intervention)
|
Differences in general attitudes towards gender will be qualitatively collected via interview from women from baseline to post intervention.
|
Baseline, End-Line (12 Months Post Intervention)
|
|
Household Food Insecurity
Time Frame: End-Line (12 Months Post Intervention)
|
Access to adequate amounts of food for the household will be assessed via interview.
|
End-Line (12 Months Post Intervention)
|
|
Change in Household Food Insecurity
Time Frame: Baseline, End-Line (12 Months Post Intervention)
|
Change in access to adequate amounts of food for the household from baseline to end-line will be assessed via interview.
|
Baseline, End-Line (12 Months Post Intervention)
|
|
Total Personal and Household Income
Time Frame: End-Line (12 Months Post Intervention)
|
The total income generated for a household will be collected via interview.
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End-Line (12 Months Post Intervention)
|
|
Change in Total Personal and Household Income
Time Frame: Baseline, End-Line (12 Months Post Intervention)
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The difference in the total income generated for a household from baseline to end-line.
|
Baseline, End-Line (12 Months Post Intervention)
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- IRB00083606
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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