- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico 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"
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
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.
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Bogota, Colombia
- Econometria Consultores
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Women who initiate and finalize the process with the comissaries of family
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: Trained
Training civil servants in Medellin (Colombia) on attention to violence against women.
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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.
|
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Sin intervención: Non trained
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Occurrence of violence
Periodo de tiempo: 3 months
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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
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3 months
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Knowledge, attitudes and practices (KAP) on violence and care pathways
Periodo de tiempo: 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
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Average of 8 months after the complaint was presented at the comissaries
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Psychological well-being (self-acceptance, positive relationships, autonomy, environmental mastery, personal growth, purpose in life)
Periodo de tiempo: Average of 8 months after the complaint was presented at the comissaries
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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
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Average of 8 months after the complaint was presented at the comissaries
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Time resolution of cases
Periodo de tiempo: 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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Colaboradores e Investigadores
Patrocinador
Colaboradores
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Otros números de identificación del estudio
- ATN/MG-13064-RG ECO 577-3
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. .