Cette page a été traduite automatiquement et l'exactitude de la traduction n'est pas garantie. Veuillez vous référer au version anglaise pour un texte source.

Assessing the Effect of Sustainable Small-scale Egg Production on Maternal and Child Nutrition in Rural Zambia

2 février 2018 mis à jour par: Cornell University

Animal source foods (ASF), such as meat and eggs, are rich in nutrients critical for growth and development. Yet, for poor children in developing countries, ASF consumption is limited by cost, inadequate caregiver knowledge, and lack of local production and physical availability. The impact of HH- and village-level livestock interventions on household dietary diversity and nutritional status in resource-poor communities is not well established. The objective of this study is to test the effectiveness of local egg production intervention on maternal and child diets and child nutrition status.

This project takes place in the Luangwa Valley, Zambia in partnership with a local non-governmental organization, COMACO. Twenty communities will be assigned to the intervention, and 20 matched communities will be selected as controls. In each intervention community, an egg production facility will be built, owned, and operated by trained COMACO farmers.

Households (HHs) in each community will be sampled twice annually for 1 year pre-intervention (baseline) and 1 year post-intervention to assess dietary diversity and nutritional status. Data analysis will test for a change in these outcomes from baseline in each intervention community compared to the matched control community.

Aperçu de l'étude

Statut

Complété

Intervention / Traitement

Description détaillée

The objective of this study is to test the effectiveness of an intervention establishing local egg production on maternal and child diets and nutrition status. The investigators hypothesize that this intervention, combined with appropriate agricultural extension and nutrition education programs, will result in: 1) increased total household, maternal, and child consumption of eggs; 2) improved maternal and child dietary quality; and 3) improved infant/ young child nutritional status.

The investigators will test this hypothesis in the Luangwa Valley, Zambia in partnership with a local non-governmental organization, Community Markets for Conservation (COMACO). The forty study sites are located in four geographic clusters (Chiefdoms) in Eastern Province Zambia. These Chiefdoms are located in two districts: Mambwe (Mnkhanya, Jumbe, and Nsefu Chiefdoms) and Lundazi (Mwanya Chiefdom).

Twenty communities will be assigned to the intervention (egg production), and 20 matched communities will be selected as controls (no intervention). In each intervention community, an egg production facility will be built, each owned and operated by trained COMACO farmers, mostly women. Each group will be provided layer pullets at point-of-lay and layer mash. Facility owners will make all business decisions, retain all profits, and will be responsible for all upkeep costs.

In a repeated cross-sectional study design, indicators of food security, wealth, diet, nutritional status (anthropometrics), and health and wellbeing will be assessed in all egg-producing HHs and in women/child dyads (children aged 6-36 months) residing in the area surrounding each facility or central control point. Data will be collected twice annually for 1 year pre-intervention (baseline) and 1 year post-intervention.

The exposure of interest is living in an egg-producing community. In the primary analysis, the investigators will use hierarchical mixed effects modeling to analyze the effect of the program on each of the outcomes of interest (see Outcome Measures section for details).

Type d'étude

Interventionnel

Inscription (Réel)

3546

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

    • Eastern Province
      • Mfuwe, Eastern Province, Zambie
        • COMACO

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

6 mois à 3 ans (Enfant)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  1. the HH dwelling is ≤1.5 km from the egg production facility or central control point;
  2. there is a child 6-36 months of age in the HH; and,

Additionally, all HHs that include a member of the egg production group will be enrolled in the study, regardless of whether or not they meet the above inclusion criteria.

Exclusion Criteria:

  1. the mother/primary caretaker or head of HH cannot converse with the field staff because of language;
  2. the mother/primary caretaker or head of HH is unable to give informed consent or complete an interview without assistance; or,
  3. the child is deformed, disabled, severely ill, or unable to cooperate for anthropometric measures.

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: Non randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Intervention
Establishment and support of a community-owned and -operated egg production facility located at a central location in the community
Aucune intervention: Contrôler

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Change in child height-for-age Z-score
Délai: 6, 12, 18, and 24 months after intervention
Recumbent length for children < 24 months and standing height for those 24-36 months, with WHO Child Growth Standards as the reference population.
6, 12, 18, and 24 months after intervention

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Change in household egg consumption
Délai: 6, 12, 18, and 24 months after intervention
7 day recall on total number of chicken or other eggs consumed in the household
6, 12, 18, and 24 months after intervention
Change in maternal egg consumption
Délai: 6, 12, 18, and 24 months after intervention
6, 12, 18, and 24 months after intervention
Change in child egg consumption
Délai: 6, 12, 18, and 24 months after intervention
6, 12, 18, and 24 months after intervention
Change in maternal dietary diversity
Délai: 6, 12, 18, and 24 months after intervention
Measured by Women's Dietary Diversity Score, a 24 hour recall of all foods consumed, organized into 9 food groups
6, 12, 18, and 24 months after intervention
Change in child dietary diversity
Délai: 6, 12, 18, and 24 months after intervention
6, 12, 18, and 24 months after intervention
Change in child stunting
Délai: 6, 12, 18, and 24 months after intervention
Defined as having a height-for-age z-score < -2.0, with WHO Growth Standards as the reference population.
6, 12, 18, and 24 months after intervention

Autres mesures de résultats

Mesure des résultats
Description de la mesure
Délai
Change in household food security
Délai: 6, 12, 18, and 24 months after intervention
Measure by Household Food Insecurity Access Scale (HFIAS), Household Hunger Scale (HHS) and/or Months of inadequate household food provisioning (MIHFP)
6, 12, 18, and 24 months after intervention
Change in producer household and poultry incomes
Délai: 6, 12, 18, and 24 months after intervention
6, 12, 18, and 24 months after intervention
Change in maternal physical and emotional health
Délai: 6, 12, 18, and 24 months after intervention
Measured through a 6-item index adapted from RAND short form
6, 12, 18, and 24 months after intervention
Change in maternal nutritional status
Délai: 6, 12, 18, and 24 months after intervention
Measured by mid-upper arm circumference and body mass index
6, 12, 18, and 24 months after intervention
Change in child weight-for-height Z-score
Délai: 6, 12, 18, and 24 months after intervention
6, 12, 18, and 24 months after intervention
Change in child weight-for-age Z-score
Délai: 6, 12, 18, and 24 months after intervention
6, 12, 18, and 24 months after intervention

Collaborateurs et enquêteurs

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

Parrainer

Les enquêteurs

  • Chercheur principal: Alexander J Travis, VMD, PhD, Cornell University

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

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 juin 2014

Achèvement primaire (Réel)

1 juillet 2016

Achèvement de l'étude (Réel)

1 mai 2017

Dates d'inscription aux études

Première soumission

3 août 2015

Première soumission répondant aux critères de contrôle qualité

4 août 2015

Première publication (Estimation)

6 août 2015

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

6 février 2018

Dernière mise à jour soumise répondant aux critères de contrôle qualité

2 février 2018

Dernière vérification

1 février 2018

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • 1402004456

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 .

S'abonner