Alive & Thrive Nigeria Impact Evaluation

Sponsor
RTI International (Other)
Overall Status
Completed
CT.gov ID
NCT02975063
Collaborator
FHI 360 (Other), University of North Carolina, Chapel Hill (Other), TNS RMS Nigeria, Ltd. (Other)
15,169
2
2
46.4
7584.5
163.4

Study Details

Study Description

Brief Summary

Investigators will use a cluster-randomized design to evaluate the overall impact of the Alive & Thrive infant and young child feeding communication strategies in Lagos and Kaduna States, Nigeria. The impact in each state and in a subset of urban local government areas (LGAs) will also be tested.This is a mixed methods evaluation; the quantitative data will be complemented by qualitative data obtained from different groups targeted by or involved in the program.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: A&T IYCF intervention
N/A

Detailed Description

Adequate nutrition during the first 1,000 days is necessary for children to grow and develop to their full potential. Alive & Thrive (A&T) contributes to better nutrition during the first 1,000 days by promoting improved infant and young child feeding (IYCF) practices. A&T is expanding its efforts to Nigeria and will target Lagos and Kaduna States. In Nigeria, 33% of infants are breastfed within 1 hour of delivery, 60% are given other fluids in the first 3 days of life, and only 17% of children 0-5.9 months are exclusively breastfed. Approximately 60% of children 6 to 23 months achieve the minimum meal frequency for their age and 19% are fed four or more food groups per day. To address these gaps in optimal IYCF practices, A&T will use an implementation framework for IYCF impact at scale that includes advocacy, interpersonal communication and community mobilization, mass communication, and strategic use of data. The A&T intervention will be compared to mass media communication on IYCF, which will be provided throughout the two states. LGAs in Lagos and Kaduna will be randomly allocated such that two-thirds receive the A&T intervention and one-third are assigned to the comparison group. The primary objectives of the evaluation are to measure the impact of the A&T intervention on IYCF practices among mothers with children 0-23 months of age overall, in each state, and in a subset of urban LGAs. Secondary evaluation objectives are to document: the type, quantity, and timing of the implementation of A&T program activities; coverage levels A&T achieves with different program activities; extent to which A&T increases knowledge and awareness of optimal IYCF practices among women with children 0 to 23 months and health providers; extent to which A&T improves the capacity of health providers to counsel mothers on IYCF; and extent to which A&T improves the capacity of stakeholders to implement community-based activities that support optimal IYCF practices.

Study Design

Study Type:
Interventional
Actual Enrollment :
15169 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Alive & Thrive Nigeria Impact Evaluation
Actual Study Start Date :
Jan 19, 2017
Actual Primary Completion Date :
Dec 2, 2020
Actual Study Completion Date :
Dec 2, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: A&T IYCF intervention

A&T IYCF intervention is includes comprehensive IYCF counseling which includes intensive activity that aims to deliver one-on-one counseling at home or in a health facility.

Behavioral: A&T IYCF intervention
(1) Interpersonal communication through frontline workers/volunteers to increase mothers' knowledge and practice of optimal infant and young child feeding (IYCF) behaviors. Interpersonal communication will involve multiple contacts with mothers and an array of IYCF messages; (2) Community mobilization activities to raise awareness of the benefits of optimal IYCF practices among opinion leaders and family members, and increase their support to mother for IYCF; (3) Training of facility and community-based health workers on IYCF to improve their ability to support mothers and provide timely information on IYCF; and (4) Mass media communication on IYCF.

No Intervention: Control

No intervention.

Outcome Measures

Primary Outcome Measures

  1. Exclusive breastfeeding on the day preceding the interview. [2 years]

    The proportion of infants 0-5 months who were exclusively breastfed on the previous day.

Secondary Outcome Measures

  1. Exclusive breastfeeding from 0-5 months. [2 years]

    The proportion of children who were exclusively breastfed from 0-5 months.

  2. Breastfeeding within 1 hour of birth. [2 years]

    The proportion of children 0-23 months who were breastfed within 1 hour of birth.

  3. Minimum dietary diversity. [2 years]

    The proportion of children 6-23 months who were fed the minimum number of food groups on the previous day based on the WHO infant and young child feeding guidelines.

  4. Minimum meal frequency. [2 years]

    Description: The proportion of children 6-23 months who were fed the minimum number of meals on the previous day based on the World Health Organization infant and young child feeding guidelines.

  5. Mothers' accurate knowledge of optimal infant and young child feeding practices. [2 years]

    Mothers' accurate knowledge of: Optimal timing of breastfeeding initiation Optimal duration of exclusive breastfeeding Solution to common breastfeeding problems Optimal timing to introduce complementary foods Optimal dietary diversity and frequency of complementary feeding from 6-23 months

  6. Health providers' knowledge of optimal infant and young child feeding practices. [2 years]

    Providers' accurate knowledge of: Optimal timing of breastfeeding initiation Optimal duration of exclusive breastfeeding Solution to common breastfeeding problems Optimal timing to introduce complementary foods Optimal dietary diversity and frequency of complementary feeding from 6-23 months

Eligibility Criteria

Criteria

Ages Eligible for Study:
15 Years to 49 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • For mother's survey:

  • Women of reproductive age (15-49 years),

  • Must be married if 15-17 years,

  • Has a child 0-23 months

  • For provider's survey:

  • Male or female,

  • 18 years or older

  • Works in a government or private health facility or works as a community pharmacist, private patent medicine vendor, or traditional birth attendant

Exclusion Criteria:

Contacts and Locations

Locations

Site City State Country Postal Code
1 Kantar TNS RMS Ikeja Lagos Nigeria
2 Kantar TNS RMS Kaduna Nigeria

Sponsors and Collaborators

  • RTI International
  • FHI 360
  • University of North Carolina, Chapel Hill
  • TNS RMS Nigeria, Ltd.

Investigators

  • Principal Investigator: Valerie Flax, RTI International
  • Principal Investigator: Mariam Fagbemi, TNS RMS Nigeria, Ltd.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
RTI International
ClinicalTrials.gov Identifier:
NCT02975063
Other Study ID Numbers:
  • 08100206
First Posted:
Nov 29, 2016
Last Update Posted:
Jan 14, 2021
Last Verified:
Aug 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by RTI International

Study Results

No Results Posted as of Jan 14, 2021