Home Fortification of Complementary Foods in Bihar India

Sponsor
Emory University (Other)
Overall Status
Completed
CT.gov ID
NCT02593136
Collaborator
(none)
11,861
1
2
21
565

Study Details

Study Description

Brief Summary

This study evaluates the program effectiveness of home fortification along with infant and young child feeding (IYCF) counseling as a strategy to address anemia and complementary feedings gaps in a program setting of the Integrated Family Health Initiative being implemented by CARE India (a non-profit organization) in partnership with the Government of Bihar. The study also seeks to assess the field level worker experience with counseling and dissemination of home fortification products.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Home Fortification Product (HFP)
  • Other: Infant and Young Child Feeding (IYCF) Practices Counseling
N/A

Detailed Description

This study evaluates the program effectiveness of home fortification along with infant and young child feeding (IYCF) counseling as a strategy to address anemia and complementary feedings gaps in a program setting of the Integrated Family Health Initiative being implemented by CARE India (a non-profit organization) in partnership with the Government of Bihar.The key objectives of this study are to examine acceptability and utilization by target population, assess impact on infant and young child feeding (IYCF) practices, evaluate impact on child growth, evaluate impact on hemoglobin concentration, and assess front line worker experience and motivation to disseminate enhanced counseling and home fortification products.

Study Design

Study Type:
Interventional
Actual Enrollment :
11861 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Assessing Feasibility and Program Effectiveness of Home Fortification of Complementary Foods in Bihar: A Cluster Randomized Community Pilot
Study Start Date :
Jun 1, 2014
Actual Primary Completion Date :
Mar 1, 2016
Actual Study Completion Date :
Mar 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: Home Fortification and Counseling

Participants aged 6 to 18 months will receive a daily supplement of vitamins and minerals in dry powder form to be taken once daily for up to nine months or up to 240 sachets. Participant caregivers will also receive improved young child feeding practices (IYCF) counseling from a front line worker.

Dietary Supplement: Home Fortification Product (HFP)
The home fortification product (HFP) is a sachet containing multiple vitamins and nutrients as follows: Iron (Ferrous Fumarate) 12.5 mg Zinc (Zinc Gluconate) 5 mg Folic Acid 0.160 mg Vitamin-A (Vit-A Acetate) 0.30 mg Vitamin-C (Ascorbic Acid) 30 mg Vitamin-B12 0.9 mcg Iodine 90 mcg Maltodextrin (Base)

Other: Infant and Young Child Feeding (IYCF) Practices Counseling
Infant and Young Child Feeding (IYCF) Practices Counseling provides direction on breast milk and milk feeding, food variety, and frequency for caregivers of children aged 6 to 18 months. Participants will be visited at least monthly by a field line worker for IYCF counseling and educational materials distribution.

Experimental: Improved Child Feeding Practices (IYCF) Counseling

Participants ages 6 to 18 months will receive improved young child feeding practices (IYCF) counseling from a front line worker.

Other: Infant and Young Child Feeding (IYCF) Practices Counseling
Infant and Young Child Feeding (IYCF) Practices Counseling provides direction on breast milk and milk feeding, food variety, and frequency for caregivers of children aged 6 to 18 months. Participants will be visited at least monthly by a field line worker for IYCF counseling and educational materials distribution.

Outcome Measures

Primary Outcome Measures

  1. Number of home fortification sachets consumed [Within 7 days (Up to 7 days)]

    The number of sachets consumed versus those received by participants within seven days of distribution.

  2. Number of home fortification sachets consumed [Within 31 days (Up to 31 days)]

    The number of sachets consumed versus those received by participants within thirty one days of distribution.

  3. Change in hemoglobin concentration [Baseline (month 0), Endline (month 12)]

    Hemoglobin concentration will be collected by taking a small blood sample via finger or heal prick. A hemoglobin level below 7 g/dl is considered severe anemia.

Secondary Outcome Measures

  1. Frequency of home visits [Up to 12 months]

    The number of times a front-line worker (FLW) visits one home within a twelve month period.

  2. Frequency of home fortification sachet distribution [Up to twelve months]

    The number of times a front-line worker (FLW) distributes home fortification sachets within a twelve month period.

  3. Change in body length [Baseline (month 0), Endline (month 12)]

    Child length will be measured using a SECA 417 length measuring board. Its measuring range is 10-100 cm with a graduation of 1 mm.

  4. Change in body weight [Baseline (month 0), Endline (month 12)]

    Child body weight will be measured using a SECA 874 mother-baby digital scale with capacity of 200 kg and graduation of 50 g < 150 kg > 100 g.

  5. Complementary Feeding Rate [Month 6 (Up to six months)]

    The percent of children initiating complementary feeding at six months.

  6. Number of daily meals [Within 24 hours (Up to one day)]

    The number of meals consumed per child in one day.

  7. Quantity of food [Within 24 hours (Up to one day)]

    The amount of food consumed by a child per meal in the home fortification and IYCF arm versus the IYCF alone arm.

  8. Consistency of foods [Within 24 hours (Up to one day)]

    The type of food textures (thick versus thin) consumed within 24 hours in the home fortification and IYCF arm versus the IYCF alone arm.

  9. Diversity of foods [Within 24 hours (Up to one day)]

    The number of different food groups consumed in one day in the home fortification and IYCF arm versus the IYCF alone arm.

  10. Front-line worker motivation [Endline (Up to 9 months)]

    Front-line worker (FLW) motivation to disseminate enhanced counseling and home fortification products will be measured at the end of study by the FLW survey. The FLW survey consists of questions regarding experience and perceived impact on work burden.

  11. Change Developmental Milestones Checklist-II (DMC-II) [Baseline (month 0), Endline (month 12)]

    Child development will be measured using the Developmental Milestones Checklist-II (DMC-II). The DMC-II is a 75-item parent report questionnaire evaluating gross motor, fine motor, language, personal-social skill development in children who are 3 to 24 months in age. The DMC-II has been slightly modified for this study by adding 7 items assessing cognitive development. The exact number of items administered depends on responses to previous items and the total range of score varies. Higher scores indicate increased development.

  12. A-not-B task performance [Endline (month 12)]

    Child executive function will be measured by direct child assessment using the A-not-B task in children 12-18 months of age only. Whether or not the child correctly identifies the location of a hidden toy is method of assessing development in early life.

  13. Elicited imitation task performance [Endline (month 12)]

    Child memory will be measured by direct child assessment using the Elicited imitation tasks in children 12-18 months of age only. Elicited imitation tasks are a tool to diagnose communication deficiencies in children. This test assesses whether or not a child can imitate the order of events of a sequence modeled by the evaluator.

Eligibility Criteria

Criteria

Ages Eligible for Study:
6 Months to 18 Months
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Randomly selected children living within Health-Sub Centers (HSC) in West Champaran Bihar
Exclusion Criteria:
  • Children less than six months of age

  • Children greater than eighteen months of age

Contacts and Locations

Locations

Site City State Country Postal Code
1 CARE-India Patna Bihar India

Sponsors and Collaborators

  • Emory University

Investigators

  • Principal Investigator: Reynaldo Martorell, PhD, Emory University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Reynaldo Martorell, Professor, Emory University
ClinicalTrials.gov Identifier:
NCT02593136
Other Study ID Numbers:
  • IRB00065311
First Posted:
Oct 30, 2015
Last Update Posted:
Mar 14, 2017
Last Verified:
Mar 1, 2017
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Reynaldo Martorell, Professor, Emory University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 14, 2017