Clinical trial Recruiting at 2 sites Observational Ages 14 and up

Understanding parental well-being after childbirth in Switzerland

Official title: Stress Of Co-parents Related to A Traumatic Experience of Birth Across Switzerland

Run by School of Health Sciences Geneva · NCT06886841 · Data updated 2026-11-12

This study looks at how new parents in Switzerland feel and cope during the first year after having a baby to see how postnatal care can be improved.

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Quick facts

Study typeObservational
Ages14 Years and up
SexAll
Enrollment4200 (estimated)
SponsorSchool of Health Sciences Geneva
Academic / other
Locations2 sites (Geneva and 1 other locations)
StatusRecruiting
StartedMarch 17, 2025
Main results expectedAugust 2025
Study endsJune 2026
Registry record updatedMarch 20, 2025
Trial IDNCT06886841 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include mothers who have recently given birth and their designated partners living with them at the time of birth.

Probably not a fit

Patients who do not meet the inclusion criteria, such as those who refuse to participate or cannot provide informed consent, may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational cohort study investigates the health and well-being of mothers and their co-parents during the first year after childbirth in Switzerland. Participants will complete four online questionnaires at various intervals: shortly after birth, and at 2, 6, and 12 months postpartum. The study aims to address the gaps in postnatal care by assessing mental distress, physical pain, and overall quality of life for both mothers and their partners. The findings are intended to inform policy and improve postnatal care practices.

Why it matters

Potential benefit: If successful, this study could lead to enhanced postnatal care practices that better support the mental and physical health of new parents.

How similar studies have gone: While there is limited research specifically on co-parent well-being post-childbirth, studies on maternal mental health have shown promising results, indicating that this approach could yield valuable insights.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion criteria:

* Women who give birth in a participating maternity unit or birth center during the study period.
* Partner of a participating women: the partner must be designated by the mother, live with her at the time of birth, and only one partner can be included per mother.
* Gestational age at birth: ≥22+0 weeks and/or birthweight ≥500 grams
* Age: Participants must be 14 years or older.
* Language Proficiency: Participants must have sufficient proficiency in one of Switzerland's main official languages (German, French, Italian) or English to ensure accurate communication and comprehension of study materials.

Exclusion Criteria:

* Refusal to participate
* Inability to provide informed consent

Where it's running

  • Haute Ecole de Santé Genève
    Geneva, Switzerland
    Recruiting
  • ZHAW Zurich University of Applied Sciences
    Winterthur, Switzerland
    Recruiting

Study contacts

  • Principal investigator: Laurent Gaucher, RM, PhD — Geneva School of Health Sciences, HES-SO University of Applied Sciences and Arts Western Switzerland, Geneva, Switzerland.
  • Study coordinator: Laurent GAUCHER, PhD
  • Email: laurent.gaucher@hesge.ch
  • Phone: +41 22 558 68 96

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.