Evaluation of Marketing Interventions in Colombia
21 augusti 2017 uppdaterad av: Kathryn Yount, Emory University
Evaluation Of The Effect Of Marketing Interventions For Women On Economic Empowerment And Risk Of Intimate Partner Violence In Colombia
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.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Detaljerad beskrivning
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.
Studietyp
Interventionell
Inskrivning (Faktisk)
1882
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
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Bogotá
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Aurora, Bogotá, Colombia
- World Food Programme Colombia
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Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
18 år till 60 år (Vuxen)
Tar emot friska volontärer
Nej
Kön som är behöriga för studier
Allt
Beskrivning
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
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Övrig
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
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Experimentell: Treatment Group 1
Farmers associations, including men and women, will be randomized to receive the smallholder marketing intervention.
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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.
|
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Experimentell: 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).
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Inget ingripande: Comparison Group 3
Women involved with farmers's associations that work independently of World Food Programmes (WFP's) assistance.
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Incidence Physical and/or Sexual IPV
Tidsram: Post-Baseline (12 Months)
|
The number of new physical and/or sexual IPV encounters as reported in the study survey.
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Post-Baseline (12 Months)
|
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Change in Prevalence of Physical and/or Sexual IPV
Tidsram: Baseline, End-Line (12 Months Post Intervention)
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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)
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Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Incidence Physical IPV
Tidsram: Post-Baseline (12 Months)
|
The number of new physical IPV encounters reported.
|
Post-Baseline (12 Months)
|
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Incidence Sexual IPV
Tidsram: Post-Baseline (12 Months)
|
The number of new sexual IPV encounters as reported in the study survey.
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Post-Baseline (12 Months)
|
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Incidence Psychological IPV
Tidsram: Post-Baseline (12 Months)
|
The number of new physiological IPV encounters as reported in the study survey.
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Post-Baseline (12 Months)
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Incidence Economic Coercion
Tidsram: Post-Baseline (12 Months)
|
The number of new encounters of economic coercion as reported in the study survey.
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Post-Baseline (12 Months)
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Change in Prevalence of Physical IPV
Tidsram: Baseline, End-Line (12 Months Post Intervention)
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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)
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Change in Prevalence of Sexual IPV
Tidsram: Baseline, End-Line (12 Months Post Intervention)
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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)
|
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Change in Prevalence of Psychological IPV
Tidsram: Baseline, End-Line (12 Months Post Intervention)
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The difference in the number of psychological IPV encounters between baseline and post intervention as reported in the study survey.
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Baseline, End-Line (12 Months Post Intervention)
|
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Change in Prevalence of Economic Coercion
Tidsram: Baseline, End-Line (12 Months Post Intervention)
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The difference in the number of economic coercion encounters between baseline and post intervention as reported in the study survey.
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Baseline, End-Line (12 Months Post Intervention)
|
Andra resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Women's Attitudes Towards Gender
Tidsram: End-Line (12 Months Post Intervention)
|
General attitudes towards gender will be qualitatively collected via interview from women post intervention.
|
End-Line (12 Months Post Intervention)
|
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Change in Women's Economic Empowerment
Tidsram: Baseline, End-Line (12 Months Post Intervention)
|
Changes in women's thoughts on economic empowerment will be qualitatively collected via interview.
|
Baseline, End-Line (12 Months Post Intervention)
|
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Change in Women's Attitudes Towards Gender
Tidsram: Baseline, End-Line (12 Months Post Intervention)
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Differences in general attitudes towards gender will be qualitatively collected via interview from women from baseline to post intervention.
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Baseline, End-Line (12 Months Post Intervention)
|
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Household Food Insecurity
Tidsram: End-Line (12 Months Post Intervention)
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Access to adequate amounts of food for the household will be assessed via interview.
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End-Line (12 Months Post Intervention)
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Change in Household Food Insecurity
Tidsram: Baseline, End-Line (12 Months Post Intervention)
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Change in access to adequate amounts of food for the household from baseline to end-line will be assessed via interview.
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Baseline, End-Line (12 Months Post Intervention)
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Total Personal and Household Income
Tidsram: End-Line (12 Months Post Intervention)
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The total income generated for a household will be collected via interview.
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End-Line (12 Months Post Intervention)
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Change in Total Personal and Household Income
Tidsram: 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.
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Baseline, End-Line (12 Months Post Intervention)
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Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Faktisk)
2 april 2016
Primärt slutförande (Faktisk)
31 juli 2017
Avslutad studie (Faktisk)
31 juli 2017
Studieregistreringsdatum
Först inskickad
5 juli 2017
Först inskickad som uppfyllde QC-kriterierna
5 juli 2017
Första postat (Faktisk)
7 juli 2017
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
22 augusti 2017
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
21 augusti 2017
Senast verifierad
1 augusti 2017
Mer information
Termer relaterade till denna studie
Andra studie-ID-nummer
- IRB00083606
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Nej
Studerar en amerikansk FDA-reglerad produktprodukt
Nej
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