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Completed

NCT Number: NCT02975063

Alive & Thrive Nigeria Impact Evaluation

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.

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Key information

Age range

15 year–49 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Kantar TNS RMS, Ikeja, Lagos, Nigeria

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About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

-

Treatment and study plan

A&T IYCF intervention

Behavioral

(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.

Primary outcomes

  1. Exclusive breastfeeding on the day preceding the interview.

    Time frame: 2 years

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

Secondary outcomes

  1. Exclusive breastfeeding from 0-5 months.

    Time frame: 2 years

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

  2. Breastfeeding within 1 hour of birth.

    Time frame: 2 years

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

  3. Minimum dietary diversity.

    Time frame: 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.

    Time frame: 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.

    Time frame: 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.

    Time frame: 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

Sponsors and collaborators

Lead sponsor

RTI International

Other

Collaborators

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

Registry information

Important dates

Study start
2017
Primary completion
2020
Study completion
2020
First posted
Nov 29, 2016
Registry last updated
Jan 14, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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