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Recruiting NCT07525830

NCT07525830 Optimizing Sleep Maternal-Offspring Bonding and Sleep in the Maternity Ward

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Clinical Trial Summary
NCT ID NCT07525830
Status Recruiting
Phase
Sponsor Centre Hospitalier Universitaire, Amiens
Condition Co-spleeping
Study Type INTERVENTIONAL
Enrollment 132 participants
Start Date 2026-02-16
Primary Completion 2027-02

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
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Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 132 participants in total. It began in 2026-02-16 with a primary completion date of 2027-02.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The quality of sleep in maternity wards is crucial for the mental and physical health of the mother, as well as for the development of secure mother to infant bonding. The introduction of "co-dodo" cribs, although scarcely studied, may influence sleep quality in both the mother and the newborn infant. Objective : This study aims at evaluating the impact of a co-dodo crib on the sleep quality of the newborn infant, her mother and the mother-infant bonding, compared to a control group with mother using a standard crib. This observational, randomized, controlled, multicenter study will include adult mother, breastfeeding and hospitalized in maternity wards after full-term delivery (≥ 37 weeks of gestation). Participant will be randomly assigned in a 1:1 ratio to receive either a co-dodo crib or a standard crib for their newborn infant during their maternity STAI-Y. Actigraphic data will be used for non-invasive sleep assessment in both the newborn infant and the mother. Validated self-reported questionnaires will evaluate maternal stress, sleep quality, post-partum depression risk and mother-infant bonding. • Hypothesis : We hypothesize that using a co-dodo crib compared to a standard crib may improve the newborn and mother sleep quality, decrease the mother stress and enhance the mother to infant bonding.

Eligibility Criteria

Inclusion Criteria: * Maternal inclusion criteria: * Mother over 18 years of age; * Mother for whom vaginal delivery is planned * Mother who has chosen to breastfeed exclusively; * Mother who has a single pregnancy; * Mother with no history of sleep disorders. * Mother able to understand, read and speak French or, failing that, who has someone in her immediate circle who can understand, read and speak French; * Mother affiliated to the social security system; * Having signed the consent to participate in the study * Newborn inclusion criteria: * Newborns born at term, i.e. ≥ 37+0 weeks of amenorrhea (SA). Exclusion Criteria: * Non-inclusion criterion relating to the mother: * Mother for whom a cesarean section is scheduled * Mother under legal protection ; * Mother presenting with an acute or chronic non-stabilized condition; * Mother with a history of sleep disorders; * Mother exposed to substances that can alter sleep (alcohol, sedative drugs). Secondary exclusion criteria: * Mother who gave birth by emergency cesarean section * Mother with a major post-partum medical complication requiring follow-up in a unit other than the maternity unit; * Newborn with a major medical complication requiring follow-up in a unit other than the maternity unit.

Contact & Investigator

Central Contact

Pierre TOURNEUX, Pr

✉ Tourneux.pierre@chu-amiens.fr

📞 33+322088051

Frequently Asked Questions

Who can join the NCT07525830 clinical trial?

This trial is open to female participants only, aged 18 Years or older, studying Co-spleeping. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07525830 currently recruiting?

Yes, NCT07525830 is actively recruiting participants. Contact the research team at Tourneux.pierre@chu-amiens.fr for enrollment information.

Where is the NCT07525830 trial being conducted?

This trial is being conducted at Amiens, France.

Who is sponsoring the NCT07525830 clinical trial?

NCT07525830 is sponsored by Centre Hospitalier Universitaire, Amiens. The trial plans to enroll 132 participants.

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