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Leveraging an Existing Large-scale Safe Water Program to Deliver Nutrition Messages at a Low Marginal Cost

17 de março de 2019 atualizado por: Marcos Vera Hernandez
The investigators are seeking to overcome the dual challenges of under-nutrition and diarrhea using an existing safe water supply platform to deliver nutrition information to targeted groups in Western Kenya. Using a randomized evaluation, investigators will determine the impact on nutrition status and practices of delivering nutrition information. The evaluation results will enable Evidence Action to make strategic decisions regarding the potential scale-up of the combined program across Kenya.

Visão geral do estudo

Descrição detalhada

Evidence Action's Dispensers for Safe Water program currently provides access to safe water for two million people. The program would be able to leverage the existence of this service delivery platform to provide promoters with training on proper nutrition and methods for delivering these messages to target groups.

The intervention is a home visiting program that will provide nutrition advice on complementary feeding to households with children aged 6-24 months. Two types of home visits will be evaluated, a 'traditional visit mode' in which the child's mother receives the visit; and a 'couples visit mode' in which the promoter attempts to involve both the father and mother.

Households in the control group will also receive home visits by promoters but the content of the visit will be restricted to safe water. The same information on safe water will also be provided to households in the treatment group. Hence, the evaluation will measure the additional effect of providing nutrition information on top of information on safe water.

Promoters will provide advice on nutrition and food hygiene to target households, according to criteria established by Evidence Action. Following the Guiding Principles for Complementary Feeding of the Breastfed Child (PAHO/WHO 2003), the intervention will include information on the maintenance of breastfeeding, safe/hygienic preparation and storage of complementary foods, amount of complementary food needed, food consistency, meal frequency and energy density, nutrient content of complementary foods, and feeding after illness. The home visits will be modelled on the MaiMwana Infant Feeding intervention (http://www.maimwana.malawi.net/MaiMwana/Home.html) that has been taking place in Mchinji (Malawi) since 2005.

Households within the treatment group will be provided by a poster to hang in their dwellings with some basic information on nutrition. A random subset of households will be given a small poster in black and white, and the other subset of households will be give a larger color poster.

Tipo de estudo

Intervencional

Inscrição (Real)

1671

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

    • Busia County
      • Busia, Busia County, Quênia
        • Evidence Action

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

Não mais velho que 1 ano (Filho)

Aceita Voluntários Saudáveis

Sim

Gêneros Elegíveis para o Estudo

Tudo

Descrição

Inclusion Criteria:

  • Children will be included if they are between 0 and 18 months at baseline and live within the catchment area of a water point in which Evidence Action installs a chlorine dispenser

Exclusion Criteria:

  • None

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Prevenção
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Solteiro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Control
Provision of information on safe water
A promoter from Evidence Action will visit the household and provide information on safe water.
Experimental: Treatment traditional
Provision of information on safe water and child nutrition. The information will be targeted to the mother of the child aged between 6 and 24 months old.
A promoter from Evidence Action will visit the household and provide information on safe water, as well as child nutrition (including hygiene on food preparation and storage). Households will be given a poster to hang in their dwellings with basic nutrition information. The poster might be smaller and in black and white, or larger and in color.
Experimental: Treatment couple
Provision of information on safe water and child nutrition. The information will be targeted to the mother of the child aged between 6 and 24 months old, and her husband.
A promoter from Evidence Action will visit the household and provide information on safe water, as well as child nutrition (including hygiene on food preparation and storage). Households will be given a poster to hang in their dwellings with basic nutrition information. The poster might be smaller and in black and white, or larger and in color.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Prazo
Height-for-age z-score
Prazo: Up to 18 months
Up to 18 months

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Knowledge of child nutrition issues measured using a structured questionnaire
Prazo: Up to 18 months
Measured using a structured questionnaire
Up to 18 months
Child nutritional intake measured using a 7 day Food Frequency Questionnaire
Prazo: Up to 18 months
Measured using a 7 day Food Frequency Questionnaire
Up to 18 months
Child's age when breastfeeding stops measured using a structured questionnaire
Prazo: Up to 18 months
Measured using a structured questionnaire
Up to 18 months
A composite index of other anthropometric indicators (includes child's weight for age z-score, child's mid-upper arm circumference, and child's head circumference)
Prazo: Up to 18 months
The composite index will include child's weight for age z-score, child's mid-upper arm circumference, and child's head circumference.
Up to 18 months
Probability that the child suffers from bipedal oedema
Prazo: Up to 18 months
Up to 18 months

Outras medidas de resultado

Medida de resultado
Descrição da medida
Prazo
Household food consumption measured using a structured questionnaire
Prazo: Up to 18 months
Measured using a structured questionnaire
Up to 18 months
Household consumption measured using a structured questionnaire
Prazo: Up to 18 months
Measured using a structured questionnaire
Up to 18 months
Total Chlorine Residual score
Prazo: Up to 18 months
Up to 18 months
Labor supply measured using a structured questionnaire
Prazo: Up to 18 months
Measured using a structured questionnaire
Up to 18 months
Time cooking on the day prior to the interview measured using a structured questionnaire
Prazo: Up to 18 months
Measured using a structured questionnaire
Up to 18 months
Women's empowerment measured using a structured questionnaire
Prazo: Up to 18 months
Measured using a structured questionnaire
Up to 18 months
Probability of having a chat with a friend or acquaintance about food or nutrition measured using a structured questionnaire
Prazo: Up to 18 months
Measured using a structured questionnaire. Having a chat in the last 3 days prior to the survey interview.
Up to 18 months
Probability of child suffering from diarrhea measured using a structured questionnaire
Prazo: Up to 18 months
Measured using a structured questionnaire. Suffering from diarrhea in the last 7 days prior to the survey. Diarrhea is defined as having 3 loose stools in any one day and/or having blood in the stools at least once.
Up to 18 months
Hygiene practices measured using a structured questionnaire
Prazo: Up to 18 months
Measured using a structured questionnaire
Up to 18 months

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Colaboradores

Investigadores

  • Investigador principal: Marcos Vera-Hernandez, PhD, research fellow

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo

1 de maio de 2015

Conclusão Primária (Real)

1 de junho de 2017

Conclusão do estudo (Real)

1 de junho de 2017

Datas de inscrição no estudo

Enviado pela primeira vez

14 de abril de 2015

Enviado pela primeira vez que atendeu aos critérios de CQ

27 de abril de 2015

Primeira postagem (Estimativa)

28 de abril de 2015

Atualizações de registro de estudo

Última Atualização Postada (Real)

19 de março de 2019

Última atualização enviada que atendeu aos critérios de controle de qualidade

17 de março de 2019

Última verificação

1 de março de 2019

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • 1827/006

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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