Evaluation of Marketing Interventions in Colombia
21. august 2017 oppdatert 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.
Studieoversikt
Status
Fullført
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
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.
Studietype
Intervensjonell
Registrering (Faktiske)
1882
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
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Bogotá
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Aurora, Bogotá, Colombia
- World Food Programme Colombia
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Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
18 år til 60 år (Voksen)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
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
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Annen
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
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Eksperimentell: 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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Eksperimentell: 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.
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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.
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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Ingen inngripen: Comparison Group 3
Women involved with farmers's associations that work independently of World Food Programmes (WFP's) assistance.
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Incidence Physical and/or Sexual IPV
Tidsramme: Post-Baseline (12 Months)
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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
Tidsramme: 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.
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Baseline, End-Line (12 Months Post Intervention)
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Incidence Physical IPV
Tidsramme: Post-Baseline (12 Months)
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The number of new physical IPV encounters reported.
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Post-Baseline (12 Months)
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Incidence Sexual IPV
Tidsramme: Post-Baseline (12 Months)
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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
Tidsramme: Post-Baseline (12 Months)
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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
Tidsramme: Post-Baseline (12 Months)
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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
Tidsramme: 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.
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Baseline, End-Line (12 Months Post Intervention)
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Change in Prevalence of Sexual IPV
Tidsramme: 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.
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Baseline, End-Line (12 Months Post Intervention)
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Change in Prevalence of Psychological IPV
Tidsramme: 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
Tidsramme: 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)
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Andre resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Women's Attitudes Towards Gender
Tidsramme: End-Line (12 Months Post Intervention)
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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
Tidsramme: Baseline, End-Line (12 Months Post Intervention)
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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)
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Change in Women's Attitudes Towards Gender
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Faktiske)
2. april 2016
Primær fullføring (Faktiske)
31. juli 2017
Studiet fullført (Faktiske)
31. juli 2017
Datoer for studieregistrering
Først innsendt
5. juli 2017
Først innsendt som oppfylte QC-kriteriene
5. juli 2017
Først lagt ut (Faktiske)
7. juli 2017
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
22. august 2017
Siste oppdatering sendt inn som oppfylte QC-kriteriene
21. august 2017
Sist bekreftet
1. august 2017
Mer informasjon
Begreper knyttet til denne studien
Andre studie-ID-numre
- IRB00083606
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
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