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

2. Februar 2018 aktualisiert von: 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.

Studienübersicht

Status

Abgeschlossen

Intervention / Behandlung

Detaillierte Beschreibung

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).

Studientyp

Interventionell

Einschreibung (Tatsächlich)

3546

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

    • Eastern Province
      • Mfuwe, Eastern Province, Sambia
        • COMACO

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

6 Monate bis 3 Jahre (Kind)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

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.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Verhütung
  • Zuteilung: Nicht randomisiert
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Intervention
Establishment and support of a community-owned and -operated egg production facility located at a central location in the community
Kein Eingriff: Kontrolle

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Change in child height-for-age Z-score
Zeitfenster: 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

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Change in household egg consumption
Zeitfenster: 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
Zeitfenster: 6, 12, 18, and 24 months after intervention
6, 12, 18, and 24 months after intervention
Change in child egg consumption
Zeitfenster: 6, 12, 18, and 24 months after intervention
6, 12, 18, and 24 months after intervention
Change in maternal dietary diversity
Zeitfenster: 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
Zeitfenster: 6, 12, 18, and 24 months after intervention
6, 12, 18, and 24 months after intervention
Change in child stunting
Zeitfenster: 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

Andere Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Change in household food security
Zeitfenster: 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
Zeitfenster: 6, 12, 18, and 24 months after intervention
6, 12, 18, and 24 months after intervention
Change in maternal physical and emotional health
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 6, 12, 18, and 24 months after intervention
6, 12, 18, and 24 months after intervention
Change in child weight-for-age Z-score
Zeitfenster: 6, 12, 18, and 24 months after intervention
6, 12, 18, and 24 months after intervention

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

  • Hauptermittler: Alexander J Travis, VMD, PhD, Cornell University

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn

1. Juni 2014

Primärer Abschluss (Tatsächlich)

1. Juli 2016

Studienabschluss (Tatsächlich)

1. Mai 2017

Studienanmeldedaten

Zuerst eingereicht

3. August 2015

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

4. August 2015

Zuerst gepostet (Schätzen)

6. August 2015

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

6. Februar 2018

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

2. Februar 2018

Zuletzt verifiziert

1. Februar 2018

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

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