Extended Pilot Project Community Based Production of Complementary Food in Ethiopia

January 30, 2018 updated by: Ethiopian Public Health Institute

Evaluate the Impact of Package of Interventions on Growth and Micronutrient Status of Infant and Young Children

The purpose of the study is to evaluate the impact of a package of interventions including production and distribution of locally produced complementary foods (via so-called "Grain-banks") and Micronutrient Powders (MNPs) supplementation, and optimized food based Complementary Feeding Recommendation, on growth and micronutrient status of infants and young children. The impact of the intervention package will be evaluated in a quasi-experimental matched-control cluster design in infants and young children between 6 - 29 months of age. The impact, outcome, and output indicators of infants/children will be assessed in cross-sectional samples at baseline, after 9 and 18 months. A total of60 pair clusters are selected in which 15 households per cluster will be identified from the eligible population. A total of 1800 children from intervention and match-controlled clusters, will be sampled in the target age groups. Qualitative and quantitative data will be collected to gather information on Knowledge, Attitude and Practice (KAP), Infant and Young Child Feeding practices, anthropometry and anemia, following the impact pathway developed for the study.

Research questions to be answered in this program evaluation are:

  1. What impact does the extended pilot (implementation of local complementary food production and MNP) have on:

    1. Growth in children 17-29 months of age
    2. Infant and Young Child Feeding practices in children (6-23m), and
    3. Anemia status in children 11-23 m?
  2. What are determining factors for the impact/no impact related to:

    1. Immediate outcomes: skills and capacity; knowledge, attitude and practices; and improved access
    2. Intermediate outcomes: utilization; provision, and ensuring enabling environment
    3. Program performance as measured by program monitoring data on output and activities?

Study Overview

Status

Completed

Detailed Description

The aim of this study is to assess the impact/effectiveness of the improved interventions on infant growth and micronutrient status so as to measure what would have happened in the absence of interventions. The study will be conducted in the same four regions in Ethiopia where the program intervention is taking place namely, Amhara, Tigray, Oromiya, and South Nations Nationalities and Peoples Region (SNNPR) regions.

  • Sample size calculations assume an expected difference of 0.2 Standard Deviation (SD) in HAZ, and 5% difference in feeding practices, 80% power, and α-error of 5%; and a cluster effect of approximately 2.
  • A total of 1800 children will be sampled in both intervention and non-intervention (control) villages. A total of 120 clusters are chosen for both groups. Each intervention cluster will be matched with a control cluster selected to be similar in geographical and ecological conditions, access to a health-care centre, status of food security and the existence of Community Based Nutrition (CBN) programme. Within each pair of clusters, households will be randomly selected after the complete listing of eligible households. A total of 15 households will be identified in each 120 clusters.
  • Demographics and socio-economic status indicators will be collected using Demographic Health Surveys (DHS) methods.
  • Infant and Young Child feeding indicators will be assessed in all children 6-23 months at baseline, mid- and endline
  • Knowledge attitude and practices concerning the intervention exposure indicators including perceptions and utilization of complementary food, MNP, and the use and perceptions on the grain banks will be assessed at baseline, mid- and endline in caregivers.

Data analysis include:

  • For demographic and socio- economic characteristics of the study participants descriptive statistics will be used.
  • To calculate the nutritional status of children 6-23 months, Epi-Info/Emergency Nutrition Action (ENA) for SMART software will be used.
  • The median (min, max) of the weight or number of MNP consumed per day during the intervention period will be calculated as measure of compliance; however analyses will be done based on intention-to-treat.
  • Qualitative data will be recorded in digital recorders which will be transcribed first to local language then to English. Then specific themes will be identified and matrices will be prepared and data will be analysed.
  • The qualitative data will be analysed separately and triangulation will be made to compare the results.
  • All analysis will be done on an intention-to-treat basis, taking into account the matched-controlled design. For continuous variables we will use linear mixed models that include cluster, household and child as random effects to account for clustered observations. Fixed effects to be included in the model are covariates such as child's sex, age, household socio-economic status and relevant baseline values. Normality will be examined by creating a Quantile-Quantile (QQ) plot and subsequent visual inspection. Equal variances will be assured with Levene's test.
  • For categorical variables mixed-effects logistic regression models will be used with random effects for cluster and households.

Study Type

Interventional

Enrollment (Actual)

1800

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Addis Ababa, Ethiopia, 1242/5456
        • Ethiopian Public Health Institute

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

6 months to 2 years (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Children between 6-23 m of age who receive Complementary Food (CF) through grain bank or commercial central production
  • Living in one of the selected clusters(for intervention and nonintervention clusters)
  • Those who receive MNP (15 sachets/month/child)
  • Receive enhanced IYCF counselling
  • Receive food based Complementary Food Recommendation (CFR)
  • Free of chronic conditions that may impact their health

Exclusion criteria:

  • Children between 6-23 m of age who do not get CF either through grain bank program or central production
  • Those who do not get MNP
  • Those who do not receive food based CFR
  • Children with a chronic disease and/or chronic use of medications

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Program evaluation in intervention areas

A quasi-experimental matched-control cluster design will be used in which outcomes are compared in intervention and non-intervention areas. The program evaluation will have three points of data collection to assess effect of the program on the nutritional status of children 6-29 months. Sixty intervention clusters have been purposively selected whereas the data will be collected from randomly selected subjects. The following interventions will be provided:

  • Processed complementary food rations will be distributed to all children 6-23 months of age, from a grain bank based on bartering of raw materials.
  • Monthly 15 sachets of MNP will be provided to all children 6-23 months of age with the instruction to add them to their complementary food, to enable point-of-use fortification.

The program activities include: processed complementary food rations which will be distributed to all children 6-23 months of age, in a grain bank based on bartering of raw materials; enhanced Infant and Young Child Nutrition (IYCN) counselling will be given to the mothers of children 6-23 month of age, using improved Behavior messages based Change Intervention (BCI) on formative research.

Monthly 15 MNPs sachets will be provided to all children 6-23 months of age with the instruction to add them to their complementary food, to enable point-of-use fortification on every alternate day.

No Intervention: Non intervention areas
A quasi-experimental matched-control cluster design will be used in which outcomes will be compared in intervention and non-intervention clusters. The program evaluation will have three points of data collection to assess effect of the program on the nutritional status of children 6-29 months. Matching sixty non-intervention clusters have been purposively selected out of the predetermined non- intervention districts whereas study subjects will be randomly selected from the identified clusters on a population based sampling method both groups. These non-intervention areas do not get processed complementary food rations and do not receive MNPs.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
% of children 17-29 months of age with HAZ < -2 SD
Time Frame: Up to 18 months
The ultimate outcomes of the program are improved nutritional status of children which include improved Z-scores for height-for-age (HAZ) according to the child growth standard.
Up to 18 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Mean height
Time Frame: Up to 18 months
Mean Height : Measured using standardized instruments
Up to 18 months
Z score:
Time Frame: Up to 18 months

Change in weight-for-length Z-score (WHZ), and weight-for-age Z-score (WAZ)

% of wasted and underweight children Number of stunted, wasted, underweight children/Number of normal childrenX100

Up to 18 months
Morbidity
Time Frame: Up to 18 months
- including incidence of acute diarrhea episodes (>3 loose stools/day)-incidence of respiratory infection episodes (cough and/or difficult breathing with or without fever, accompanied by rapid breathing and chest in drawing) in the last 2 weeks prior to the survey
Up to 18 months
Anemia status
Time Frame: Up to 18 months
Hemoglobin level as measured by Hemocue and adjusted for altitude
Up to 18 months
% of children 6-23 months of age who were fed an minimum acceptable diet
Time Frame: Up to 18 months
Measured using 24 hr recall method
Up to 18 months
Mean weight
Time Frame: Up to 18 months
Mean weight: Measured using standardized instruments
Up to 18 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

March 1, 2015

Primary Completion (Actual)

May 1, 2016

Study Completion (Actual)

August 1, 2017

Study Registration Dates

First Submitted

June 16, 2015

First Submitted That Met QC Criteria

June 24, 2015

First Posted (Estimate)

June 29, 2015

Study Record Updates

Last Update Posted (Actual)

January 31, 2018

Last Update Submitted That Met QC Criteria

January 30, 2018

Last Verified

February 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • EPHI_FSNRD_CF_MNP002

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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