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

17 mars 2019 mis à jour par: 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.

Aperçu de l'étude

Description détaillée

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.

Type d'étude

Interventionnel

Inscription (Réel)

1671

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

    • Busia County
      • Busia, Busia County, Kenya
        • Evidence Action

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

Pas plus vieux que 1 an (Enfant)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Tout

La description

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

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: La prévention
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Seul

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Control
Provision of information on safe water
A promoter from Evidence Action will visit the household and provide information on safe water.
Expérimental: 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.
Expérimental: 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.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Délai
Height-for-age z-score
Délai: Up to 18 months
Up to 18 months

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Knowledge of child nutrition issues measured using a structured questionnaire
Délai: Up to 18 months
Measured using a structured questionnaire
Up to 18 months
Child nutritional intake measured using a 7 day Food Frequency Questionnaire
Délai: 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
Délai: 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)
Délai: 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
Délai: Up to 18 months
Up to 18 months

Autres mesures de résultats

Mesure des résultats
Description de la mesure
Délai
Household food consumption measured using a structured questionnaire
Délai: Up to 18 months
Measured using a structured questionnaire
Up to 18 months
Household consumption measured using a structured questionnaire
Délai: Up to 18 months
Measured using a structured questionnaire
Up to 18 months
Total Chlorine Residual score
Délai: Up to 18 months
Up to 18 months
Labor supply measured using a structured questionnaire
Délai: 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
Délai: Up to 18 months
Measured using a structured questionnaire
Up to 18 months
Women's empowerment measured using a structured questionnaire
Délai: 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
Délai: 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
Délai: 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
Délai: Up to 18 months
Measured using a structured questionnaire
Up to 18 months

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Collaborateurs

Les enquêteurs

  • Chercheur principal: Marcos Vera-Hernandez, PhD, Research Fellow

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude

1 mai 2015

Achèvement primaire (Réel)

1 juin 2017

Achèvement de l'étude (Réel)

1 juin 2017

Dates d'inscription aux études

Première soumission

14 avril 2015

Première soumission répondant aux critères de contrôle qualité

27 avril 2015

Première publication (Estimation)

28 avril 2015

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

19 mars 2019

Dernière mise à jour soumise répondant aux critères de contrôle qualité

17 mars 2019

Dernière vérification

1 mars 2019

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • 1827/006

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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