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Evaluation of Marketing Interventions in Colombia

21 de agosto de 2017 actualizado por: 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.

Descripción general del estudio

Estado

Terminado

Condiciones

Intervención / Tratamiento

Descripción detallada

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.

Tipo de estudio

Intervencionista

Inscripción (Actual)

1882

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

  • Colombia
    • Bogotá
      • Aurora, Bogotá, Colombia
        • World Food Programme Colombia

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años a 60 años (Adulto)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

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

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Otro
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Treatment Group 1
Farmers associations, including men and women, will be randomized to receive the smallholder marketing intervention.
Otro: Smallholder Marketing
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.
Otro: Smallholder Marketing
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.
Otro: Intimate Partner Violence (IPV) Prevention Training
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).
Sin intervención: Comparison Group 3
Women involved with farmers's associations that work independently of World Food Programmes (WFP's) assistance.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Incidence Physical and/or Sexual IPV
Periodo de tiempo: 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
Periodo de tiempo: 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)

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Incidence Physical IPV
Periodo de tiempo: Post-Baseline (12 Months)
The number of new physical IPV encounters reported.
Post-Baseline (12 Months)
Incidence Sexual IPV
Periodo de tiempo: Post-Baseline (12 Months)
The number of new sexual IPV encounters as reported in the study survey.
Post-Baseline (12 Months)
Incidence Psychological IPV
Periodo de tiempo: Post-Baseline (12 Months)
The number of new physiological IPV encounters as reported in the study survey.
Post-Baseline (12 Months)
Incidence Economic Coercion
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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)

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Women's Attitudes Towards Gender
Periodo de tiempo: 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)
Change in Women's Economic Empowerment
Periodo de tiempo: 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)
Change in Women's Attitudes Towards Gender
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: End-Line (12 Months Post Intervention)
The total income generated for a household will be collected via interview.
End-Line (12 Months Post Intervention)
Change in Total Personal and Household Income
Periodo de tiempo: Baseline, End-Line (12 Months Post Intervention)
The difference in the total income generated for a household from baseline to end-line.
Baseline, End-Line (12 Months Post Intervention)

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Emory University

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

2 de abril de 2016

Finalización primaria (Actual)

31 de julio de 2017

Finalización del estudio (Actual)

31 de julio de 2017

Fechas de registro del estudio

Enviado por primera vez

5 de julio de 2017

Primero enviado que cumplió con los criterios de control de calidad

5 de julio de 2017

Publicado por primera vez (Actual)

7 de julio de 2017

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

22 de agosto de 2017

Última actualización enviada que cumplió con los criterios de control de calidad

21 de agosto de 2017

Última verificación

1 de agosto de 2017

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • IRB00083606

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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