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New study aims to decode how french parents choose to feed their babies

NCT ID NCT07620704

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Recruiting now
This trial is taking on new participants right now.
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Registered, but not yet taking participants.
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Paused for now. It may or may not start again.
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The trial has finished. Results may not be published yet.
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Stopped early, before it reached the end. That can be for many reasons, including safety.
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Cancelled before anyone took part.

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Not a trial. The treatment could once be requested outside a study, but no longer can.
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The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

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

Summary

This study has two parts. First, it will adapt a questionnaire called the Iowa Infant Feeding Attitude Scale for use in France, testing its accuracy with new mothers and co-parents. Second, it will survey pregnant women and their partners to understand their cultural beliefs about feeding babies. The goal is to better support families in making informed feeding choices.

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 930 people

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

Expected to start

May 2026

An estimate. Start dates often move.

Expected to finish

Jan 2029

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

For part 1, Our target population will consist of new parents during their stay in the maternity ward at one of the Auvergne Perinatal Network maternity participating in the study. For part 2, our target population will be expectant parents during pregnancy who are receiving care within the Auvergne Perinatal Network. Participation by both parents is not required for this study.

Ages

18 years and older

Sex

Anyone

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.

Part 1 Inclusion Criteria: * Adult women hospitalized for postpartum care in one of the 10 maternity hospitals of the Auvergne perinatal network participating in the project, and/or adult co-parents whose partner is hospitalized in one of the 10 RSPA maternity hospitals participating in the project, * Mothers and/or co-parents of a singleton child born alive at term (≥37 weeks' gestation) and hospitalized in the maternity ward, * Mothers and/or co-parents of a child less than 6 days old, * Mothers and/or co-parents affiliated to a social security scheme, * Mothers and/or co-parents capable of reading and understanding French. Non-inclusion Criteria: * Mothers and/or co-parents of a child hospitalized outside the maternity ward, * Mothers and/or co-parents who are adults with legal incapacity (under guardianship, conservatorship, or judicial protection), * Mothers and/or co-parents who refuse to participate in the study, * Mothers with a contraindication to AM and/or co-parents whose spouse has a contraindication to AM, * Mothers and/or co-parents of a child with a medical condition or malformation that affects their feeding. Part 2 during 1st trimester : Inclusion Criteria: * Pregnant adult women who are being cared for by healthcare professional belonging the Auvergne perinatal network and/or their co-parents of legal age, during the first trimester of pregnancy (before 16 weeks and 0 days of gestation), * Pregnant women and/or co-parents affiliated to a social security scheme, * Pregnant women and/or co-parents who can read and understand French. Non-inclusion criteria : * Pregnant women and/or co-parents in the second trimester of pregnancy (between 16 weeks 0 days and 28 weeks 6 days of gestation), * Pregnant women and/or co-parents who are legally incapacitated adults (under guardianship, conservatorship, or judicial protection), * Pregnant women and/or co-parents who refuse to participate in the study, * Pregnant women with a contraindication to breastfeeding and/or co-parents whose partner has a contraindication to breastfeeding, * Pregnant women with a multiple pregnancy and/or co-parents being monitored for a multiple pregnancy. Part 2 during 3rd trimester : Inclusion Criteria: * Pregnant adult women who are being cared for by healthcare professional belonging the Auvergne perinatal network and/or their co-parents of legal age, during the third trimester of pregnancy (after 28 weeks and 6 days of gestation), * Pregnant women and/or co-parents affiliated to a social security scheme, * Pregnant women and/or co-parents who can read and understand French. Non-inclusion criteria : * Pregnant women and/or co-parents in the second trimester of pregnancy (between 16 weeks 0 days and 28 weeks 6 days of gestation), * Pregnant women and/or co-parents who are legally incapacitated adults (under guardianship, conservatorship, or judicial protection), * Pregnant women and/or co-parents who refuse to participate in the study, * Pregnant women with a contraindication to breastfeeding and/or co-parents whose partner has a contraindication to breastfeeding, * Women and/or co-parents of a child with a medical condition or malformation affecting the child's feeding, * Pregnant women with a multiple pregnancy and/or co-parents being monitored for a multiple pregnancy.

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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.

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.

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  3. A doctor treating you

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Contacts and locations

Locations

  • CHU de Clermont-Ferrand

    Clermont-Ferrand, France, 63000, France

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