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Completed

NCT Number: NCT05016895

REACH2: Implementation Research on Bi-Annual Mass Distribution of Azithromycin to Children 1-11 Months in Côte d'Ivoire

REACH2 is a three-year implementation research study designed to examine the implementation through a mass drug administration platform of bi-annual single-dose azithromycin to reduce child mortality among children ages 1 to 11 months who reside in high child mortality settings.

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Key information

Conditions

Age range

1 month–11 month

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

FHI 360

Abidjan, Côte d’Ivoire

About this study

The aim of the study is to provide the government of Côte d'Ivoire and other stakeholders the information needed to understand what is required to bring bi-annual mass drug administration (MDA) of single-dose azithromycin for children ages 1 to 11 months in high child mortality settings to scale using the existing MDA platform used for trachoma and other neglected tropical diseases.

Design: The serial cross-sectional study will be carried out in 19 health districts in coordination with the trachoma MDAs over the course of three years. The intervention under study will involve a public health campaign of bi-annual distribution of single-dose azithromycin, including:

  • Expanded coverage with azithromycin during annual trachoma MDAs to children 1-5 months of age when delivered at the same time as the annual trachoma MDA, which already covers children 6-11 months, followed by
  • Stand-alone MDAs targeting children 1 to 11 months delivered at the approximately 6-month interval between annual trachoma MDAs, or bi-annually in areas where the annual trachoma MDAs are phased out.

To study scale up of these intervention activities, the investigators will systematically collect data, guided by the Reach, Effectiveness, Adoption, Implementation and Maintenance (RE-AIM) implementation science framework. Data collection activities will involve:

  • Analyses of routine monitoring, process, and adverse drug reaction data from the trachoma MDA platform into which the REACH activities are being integrated
  • Periodic, cross-sectional, post-MDA surveys to verify coverage and examine exposure to project information/messaging
  • Qualitative data collection through in-depth interviews (IDI) and/or focus group discussions (FGD) with parents or primary caregivers of children ages 1 to 11 months in the 19 health districts, and district-level MDA implementers to explore issues of acceptability, communication, challenges and areas for improvement in implementation.

Further, after the first round of the annual trachoma MDA scheduled to take place in July 2021, a round of focus groups will be carried out with parents of children ages 1-11 months and local implementers to inform message development for the public health campaign.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Ages 1 to 11 months
  • Resident in targeted community

Exclusion criteria

  • Children below 3.0 kg (3rd centile for healthy 1-month old infants in the WHO growth charts)
  • Appears seriously ill at the time of the MDA (per the CDD's assessment)
  • Unable to swallow liquid delivered through a needle-less syringe because of physical limitations
  • Known allergy to macrolides, including azithromycin, based on the primary caregiver's report of prior adverse reaction to medication likely to be a macrolide
  • prior allergic reaction to medication likely to be a macrolide

Treatment and study plan

Single-dose azithromycin

Drug

Bi-annual mass, community-based distribution of single-dose azithromycin to children ages 1 to 11 months.

Primary outcomes

  1. % of eligible population covered by intervention

    Time frame: three years

    coverage of the intervention's target population (reach) with azithromycin in targeted health districts

  2. Infant mortality rate

    Time frame: three years

    Rate of child deaths among children under 1 year of age per 1,000 population

  3. Implementation fidelity

    Time frame: three years

    Proportion of intervention activities are carried out as planned

Secondary outcomes

  1. Cost of the program as a whole

    Time frame: three years

    Program costs will be calculated based on the following inputs: personnel, supplies/recurrent goods, capital goods, travel/transport, space, services, and training

  2. Cost per child treated

    Time frame: three years

    Program costs per child treated

  3. Cost per death averted

    Time frame: three years

    Program costs per death averted

Sponsors and collaborators

Lead sponsor

FHI 360

Other

Collaborators

  • Ministry of Health, Ivory Coast

Registry information

Official study title

The Resiliency Through Azithromycin for Children Project: Implementation Research on Bi-Annual Mass Distribution of Azithromycin to Children 1-11 Months in Côte d'Ivoire

Acronym: REACH

Important dates

Study start
2021
Primary completion
2024
Study completion
2024
First posted
Aug 23, 2021
Registry last updated
Mar 4, 2025

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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