- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02136966
Joint Infant and Young Child Nutrition Program and Malnutrition Prevention
Joint Infant and Young Child Nutrition Program in Burkina Faso : Impact Evaluation
Study title: Joint Infant and young children nutrition program in Burkina Faso: Impact evaluation Hypothesis: The fortification of complementary foods associated with a counseling on feeding practices for infants and young children prevents malnutrition in 6-23 months-old children.
Objective: to assess the effectiveness of a promotional care package in preventing malnutrition among children aged 6-23 months.
Study Overview
Status
Intervention / Treatment
Detailed Description
The 'Institut de Recherche en Sciences de la Santé (IRSS)', in collaboration with Micronutrient Initiative (MI), the Institute of Tropical Medicine (ITM) Antwerp (Belgium), and the Health District of Tougan, will conduct a study to assess the effectiveness of a promotional package in the prevention and management of malnutrition among children aged 6-23 months.
This promotional package includes:
- A monthly follow-up sessions promoting growth in which detailed advice on feeding practices infant and young child feeding (IYCF) will be given to the mothers of children 6-23 months . These behavioral change informations be developed based on the rapid assessment of practices and foods available in the community and adaptation of the WHO manual.
- The distribution of micronutrient powders (MNP) (15 micronutrients) to mothers of children 6-23 months of age for home fortification of complementary foods
- Intensive counseling sessions and cooking demonstrations every two weeks for moderately malnourished children . Cooking demonstrations will include instructions on adding micronutrient powders and oil to meals .
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Kadiogo
-
Ouagadougou, Kadiogo, Burkina Faso
- LANOU Hermann Bienou
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Mothers of 6 to 23 months old children
- Reside in the study area
- Accept to use MNP
Exclusion Criteria:
- Mothers of children aged less than 6 months or more than 23 months.
- Refusal
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Programme
|
Growth monitoring and promotion sessions will take place every month at village level for all children 0-23 months of age and will serve as an entry point for all the interventions.
During these sessions children under 24 months will be weighed monthly and screened for MAM and uncomplicated SAM for treatment in the community as well as complicated SAM for referral to health facility During the monthly sessions cooking demonstrations will take place in which the community Health workers will instruct the mother how to prepare a good complementary food for 6-23 months olds adding the MNP.
These meals will be given to the child during the session.
Mothers will be encouraged to prepare the same meal at home During the monthly sessions enhanced IYCN counseling will be given to the mothers of 6-23 months olds, using improved BCI messages developed based on the rapid assessment of practices and foods available in the community and adaptation of the WHO manual.
|
No Intervention: Controle
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Proportion of children with Weight-for-height and/or Height-for-age ZScore <-2
Time Frame: 1 year
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Proportion of mothers who can describe at least 3 best practices about IYCN
Time Frame: 3, 6 and 12 months
|
3, 6 and 12 months
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of children with adverse events as a safety measure of the use of Micronutrient Powder for food fortification at home
Time Frame: 1 year
|
The morbidity will be assess every week from baseline until the end of the intervention (1 year)
|
1 year
|
Collaborators and Investigators
Investigators
- Principal Investigator: Hermann Lanou, MSc, Institut de Recherche en Sciences de la Santé (IRSS), Ouagadougou, Burkina Faso
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRSS0002
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