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Improving Routine Immunization Coverage Through Educational Messages Delivered During Polio NIDs in Pakistan: A Cluster Randomized Trial

0 criterios cumplidosConsulta de un vistazo cómo tu perfil cumple con cada criterio de elegibilidad.
Qué se está evaluando

Vaccine promotion messages

+ Distribution of Plastic Pouches to retain vaccination card

+ Vaccination Verification.

ConductualOtro
Quiénes están siendo reclutados

Enfermedades Neuroinflamatorias+10

+ Enfermedades del Sistema Nervioso Central

+ Infecciones del Sistema Nervioso Central

Entre 3 y 14 meses
+6 Criterios de eligibilidad
Ver todos los criterios de elegibilidad
Cómo está diseñado el estudio

Estudio de Investigación en servicios de salud

Intervencional
Inicio del estudio: abril de 2012
Ver detalles del protocolo

Resumen

Patrocinador PrincipalAga Khan University
Última actualización: 16 de enero de 2014
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Fecha de inicio: 1 de abril de 2012

Fecha en la que se inscribió al primer participante.

The overall objective of this study is to assess whether supplementary immunization activities (SIAs) held for polio eradication can be used to improve routine immunization coverage in Pakistan. Primary research objectives: (i) To assess effectiveness of educational messages regarding routine immunization during SIAs held for polio on improving routine immunization coverage in Pakistan. Secondary research objectives: (i) To assess maternal knowledge about routine immunization in the intervention and control arms. (ii) To estimate vaccination card retention in the intervention and control arms. This study will be completed in 12 months, between March 2012 to February 2013. Overall, three major operational steps have been defined for the study as follow: Baseline vaccine coverage survey: This is a 02-months activity in which a baseline household vaccine coverage survey will be carried out to independently assess the immunization coverage and socio-demographic indicators in the study areas. Participation in this survey will be voluntary and written consent from participants will be obtained prior to administering the study questionnaire. Training of vaccinators/volunteers and distribution of plastic pouches: The project research staff (Research Associate/Senior Research Assistants) will be exclusively trained by Principal Investigator/Research Supervisor on educational material. Having completed the baseline coverage survey, a one-day training session will be organized by trained project staff to provide trainings to participating EPI vaccinators/volunteers on the vaccine promotion educational messages to be delivered during intervention. These trainings will be held at a common venue (EPI center/public hospital) in the selected towns for this study. The messages will be low-literacy, of very short duration, and will be delivered with the help of pictorial cards which were previously developed for and used in a similar department-run study in Karachi. These educational messages will include the following messages: Vaccines can save a child's life Children who are immunized on time are less likely to become ill Unimmunized children can become disabled for life Photograph of the nearest EPI center where vaccines are offered free of charge, as well as its address and timings Additionally, at the start of this project, all EPI centers in the study areas will be provided with plastic pouches to be given to parents of all children coming to EPI centers for vaccinations. These pouches will be used to store a child's immunization card. In order to assess the likely change in vaccination card retention, we will compare the proportion of vaccination cards available on pre-and-post coverage assessment in both intervention and control groups. Endline vaccine coverage survey/outcome assessment. Outcome assessment will be done through a representative endline survey assessing vaccine coverage for Penta-3 and Measles-1 in the study areas, 3 months after the NID was held. Participation in this survey will be voluntary and written consent from study participants will be obtained prior too administering the study questionnaire. NID = National Immunization Days SNID = Sub-national Immunization Days EPI: Expanded Programme on Immunization SIA - Supplementary Immunization Activity CHW = Community Health Worker AKU = Aga Khan University, Karachi, Pakistan

Patrocinador PrincipalAga Khan University
Última actualización: 16 de enero de 2014
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Protocolo

Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.
Detalles del Diseño

Se reclutarán 4560 pacientes

Número total de participantes que el ensayo clínico espera reclutar.

Estudio de Investigación en Servicios de Salud

Estos estudios analizan cómo se brinda, organiza y gestiona la atención médica. Su objetivo es mejorar la calidad del cuidado, la experiencia del paciente y el acceso al tratamiento.



Elegibilidad

Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.
Condiciones
Criterios

Cualquier sexo

Sexo biológico de los participantes elegibles para inscribirse.

Entre 3 y 14 meses

Rango de edades de los participantes que pueden unirse al estudio.

Voluntarios sanos permitidos

Indica si personas sanas, sin la condición que se estudia, pueden participar.

Condiciones

Patología

Enfermedades NeuroinflamatoriasEnfermedades del Sistema Nervioso CentralInfecciones del Sistema Nervioso CentralInfecciones por enterovirusInfeccionesMielitisEnfermedades del sistema nerviosoEnfermedades NeuromuscularesInfecciones por PicornaviridaeInfecciones por virus de ARNEnfermedades de la médula espinalEnfermedades ViralesPoliomielitis

Criterios

3 criterios de inclusión requeridos para participar
Households with children aged 3-14 months

Resident of selected cluster

Willing to consent for participation in the study

3 criterios de exclusión impiden participar
Households with children aged below 3 months or above 14 months

Non-resident of selected cluster

Refusing to consent

Plan de Estudio

Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.
Grupos de Tratamiento
Objetivos del Estudio

4 grupos de intervención están designados en este estudio

0% de probabilidad de ser asignado al grupo placebo

Grupos de Tratamiento

Grupo I

Experimental
EPI vaccinators/volunteers will educate mothers/care-providers of infants less than 12 months old months about the benefits of routine immunization

Grupo II

Experimental
EPI vaccinators/volunteers will identify and record details of un/under-vaccinated children less than 12 months old in households they visit during an NID, and update immunization registries maintained at the local EPI centers so these children can be reached in subsequent outreach activity.

Grupo III

Experimental
EPI vaccinators/volunteers will educate mothers/care-providers of infants less than 12 months old months about the benefits of routine immunization, identify and record details of un/under-vaccinated children in households they visit during an NID, and update immunization registries maintained at the local EPI centers so these children can be reached in subsequent outreach activity.

Grupo IV

Sin Intervención
No interventional activity will take place in this group. Therefore, the status quo (routine services) will be maintained during Polio NID

Objetivos del Estudio

Objetivos Primarios

Objetivos Secundarios

Centros del Estudio

Estos son los hospitales, clínicas o centros de investigación donde se lleva a cabo el estudio. Puedes encontrar la ubicación más cercana a ti y su estado de reclutamiento.

Este estudio tiene una ubicación

Thatta, Hyderabad

Thatta, Hyderabad, PakistanAbrir Thatta, Hyderabad en Google Maps
Completado1 Centros de Estudio