Midwife-Led birth units may boost Parents' mental health years after childbirth
NCT ID NCT06630741
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study follows couples who gave birth in either a midwifery-led birth unit or a standard obstetric unit in France. Researchers want to see if the type of care affects parents' mental health, especially post-traumatic stress, and the child's development up to two years later. The study includes low-risk pregnancies and aims to understand whether less medicalized care can improve long-term well-being.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Alternative midwifery birth unit (AMU) care model
- What this could lead to
- If this study shows benefits, it could support expanding midwifery-led birth units as a standard option for low-risk pregnancies, potentially improving parents' mental health and child outcomes.
- What could go wrong
- This is an observational follow-up study, not a randomized trial, so results may show associations but not prove cause and effect. Differences in outcomes could be due to other factors, and the findings may not apply to all settings.
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
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793 people
The number who actually took part.
- Started
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Oct 2024
- Finished
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May 2025
- Lead sponsor
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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
Women who gave birth in a maternity hospital involved in the study, with a low-risk pregnancy and their co-parent
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide 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: * Women who participated in the PhysioCare study, as well as the already included first-time parents partners. * Non-first-time parent partners who received information about the PhysioCare study but did not participate. * Having been informed about the protocol and not having expressed opposition to participate in the PhysioCare study. Non-inclusion Criteria: * Participant who has withdrawn his/her consent to participate in the PhysioCare study * Participant excluded from the PhysioCare study * Death of the child since the last questionnaire was entered * Adults under legal protection (safeguard of justice, curatorship, guardianship) and persons deprived of liberty.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Centre Hospitalier Simone Veil
Eaubonne, 95600, France
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Clinique Mutualiste la Sagesse
Rennes, 35000, France
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Rennes University Hospital
Rennes, 35000, France