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New study tests buddy system to boost breastfeeding in struggling moms

NCT ID NCT07499466

Knowledge-focused Sponsor: Hospices Civils de Lyon Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study is testing a program where trained volunteer mothers provide breastfeeding support to new mothers who are facing severe poverty, housing problems, or other major challenges. The goal is to see if this kind of peer support is acceptable and practical for these families. About 50 mothers will take part, and researchers will track how many complete the program and interview participants to learn what helps or hinders breastfeeding support.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 50 people

The number the study aims to enrol. It can still change while the study runs.

Started

Dec 2025

Expected to finish

Dec 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The study population consists of mothers experiencing severe socioeconomic deprivation with an infant hospitalized in the maternity or neonatal unit at the Hôpital Femme Mère Enfant (HFME), France. Eligible participants are adult mothers (≥18 years) who intend to breastfeed, have sufficient proficiency in French or a language spoken by available peer supporters, and provide oral agreement to participate. Mothers will be identified and recruited during their hospital stay. Approximately 20 eligible mothers are seen monthly in the unit. Based on eligibility criteria, expected refusal rates, and peer supporter availability (maximum two concurrent supports per peer), an estimated 5 to 8 mothers will be enrolled per month over 6 months, for a total sample of approximately 30 to 50 participants. Exclusion criteria include medical contraindications to breastfeeding, infants with life-threatening conditions, severe psychiatric conditions incompatible with participation, and legal guardianship.

Ages

18 years and older

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Mother with at least one infant hospitalized in the maternity or neonatal unit at the Hôpital Femme Mère Enfant (HFME) * Who Intents to breastfeed * Who is in a severe socioeconomic deprivation * Having sufficient proficiency in French or in one of the languages spoken by the available peer supporters to allow communication * Aged 18 years or older * Given verbal consent to participate in the study Exclusion Criteria: * \- Having a medical contraindication to breastfeeding * Having an infant with a known congenital condition with life-threatening prognosis * Having a severe psychiatric condition considered incompatible with participation in the peer-support intervention * Being under legal guardianship

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Conditions

The condition(s) this trial relates to.

Breast Feeding

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Breastfeeding Breastfeeding support Health disparities Health inequalities

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Service de néonatologie Hôpital Femme Mère Enfant

    RECRUITING

    Bron, France, 69500, France

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Other studies related to the condition(s) this trial covers.