Health Mediation Program in the Maternity Ward to support breastfeeding
Official title: Evaluation of a Health Mediation Program in the Maternity Ward.
Run by Centre Hospitalier de Cayenne · NCT07806942 · Data updated 2026-11-12
This observational study tests whether a health mediator program in the maternity ward helps new mothers in French Guiana breastfeed exclusively longer after birth.
Quick facts
| Study type | Observational |
|---|---|
| Sex | Women only |
| Enrollment | 960 (estimated) |
| Sponsor | Centre Hospitalier de Cayenne Academic / other |
| Locations | 1 site (Cayenne, Guyane) |
| Status | Recruiting |
| Started | May 26, 2026 |
| Main results expected | May 31, 2029 |
| Study ends | May 31, 2029 |
| Registry record updated | September 8, 2026 |
| Trial ID | NCT07806942 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Women who gave birth at the French Guiana University Hospital Center and consent to participate.
✕Probably not a fit
Some participants may not experience a change in breastfeeding duration or exclusivity despite the intervention.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational project analyzes breastfeeding practices among mother–infant pairs in French Guiana, focusing on the impact of postpartum support from a health mediator versus standard care. It draws on data from 382 mother–child pairs enrolled between March and October 2024, and includes a qualitative component with 15 mothers facing multidimensional vulnerability to understand barriers to exclusive breastfeeding. The study examines how in-hospital support, formula supplementation, and family or social support influence breastfeeding duration and exclusivity, with findings intended to align feeding practices with national and international recommendations. The health mediator intervention is compared to routine care to observe potential effects on breastfeeding continuation and exclusivity up to several months postpartum.
Why it matters
Potential benefit: If successful, the program could improve exclusive breastfeeding rates and infant health outcomes by providing targeted postpartum support.
How similar studies have gone: Previous data suggest that in-hospital breastfeeding support can positively influence continuation, but results vary by setting and population.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Women who gave birth at the French Guiana University Hospital Center Exclusion Criteria: * Women refusal to participate to the study or lack of opposition collected * lack of authorization from legal representatives for underage women or from legal guardians for women under legal protection * foetal death, stillbirth, or neonatal death * feeding with formula from birth
Where it's running
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Centre hospitalier de Cayenne
Cayenne, Guyane, French Guiana Recruiting
Study contacts
- Study coordinator: Célia BASURKO, MD
- Email: celia.basurko@ch-cayenne.fr
- Phone: +594594395050
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.