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Study to reveal best visiting policies for new Moms' mental health

NCT ID NCT07653646

Knowledge-focused Sponsor: Centre Hospitalier Annecy Genevois Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study looks at how different visitor policies in maternity wards impact mothers' mental health and newborn health. Researchers will survey 8,000 women in France about their postpartum experience and screen for depression. The goal is to create science-based guidelines for hospital visits that support recovery and bonding.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this could lead to evidence-based recommendations for maternity ward visiting policies that improve mothers' mental health and newborn outcomes.
What could go wrong
This is an observational study, not a treatment trial, so it won't directly test a new therapy. Results may vary across hospitals and may not apply everywhere.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 8,000 people

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

Expected to start

Jun 2026

An estimate. Start dates often move.

Expected to finish

Jun 2028

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.

Ages

18 years and older

Sex

Female participants only

Healthy volunteers

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

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

Inclusion Criteria: * Adult female patient (aged 18 or over), * Female patient admitted to the maternity ward with her newborn baby or babies, * Length of stay in the maternity ward of 48 hours or more, * Female patient who has been informed about the study and has given her free, informed verbal consent to participate in the study. Exclusion Criteria: * Patients who have already participated in this study, * Patients whose newborn(s) are hospitalised in neonatal units, neonatal intensive care units or neonatal resuscitation units, * Patients who have given birth to three or more newborns (triplets or more), * Patient whose newborn(s) has/have died, * Patient unable to understand spoken or written French, making self-assessment impossible, * Patient under guardianship, curatorship or placed under judicial protection, * Patient not covered by the French social security system.

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Conditions

The condition(s) this trial relates to.

puerperal disorder

As listed by the trial registrant

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

Newborn health Post partum women

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

  • CH Annecy Genevois

    Épagny, Auvergne-Rhône-Alpes, 74370, France

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