Evaluating information given to parents during prenatal consultations

Is this trial a fit for you?

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

What this trial studies

This observational study aims to assess how well the information provided to parents during antenatal consultations aligns with their experiences after childbirth. It involves administering a questionnaire to parents who attended consultations with a pediatric neonatologist and whose newborns were hospitalized in the neonatology department. The study focuses on understanding the quality of information regarding congenital anomalies and prematurity. By analyzing the responses, researchers hope to identify gaps in communication and improve future antenatal consultations.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patients were observed at the multidisciplinary prenatal diagnosis centre.
* Patients who had attended at least one antenatal consultation with a pediatric neonatologist
* Patients who gave birth between January 2020 and December 2022 and whose newborn was hospitalized in the neonatology department

Exclusion Criteria:

* a child who died in hospital or had a condition with a high risk of death in the first few years of life
* non-French speaking mothers
* Mothers who were minors at the time of the study

Where it's running

• Femme Mère Enfant Hospital (HFME)
  Bron, France Recruiting

Study contacts

• Study coordinator: Cosima BABINET
• Email: cosima.babinet@chu-lyon.fr
• Phone: +33608161034

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

• Household, wellbeing, and quality-of-life impacts of very preterm birth and necrotising enterocolitis

  This project will collect information to see if pausing or continuing milk feeds around blood transfusions relates to babies' quality of life and the financial and emotional impact on families of very preterm infants, especially those with NEC.

  Recruiting at 7 sites Imperial College London · Norwich, Norfolk and 6 other locations · NCT07192393

• Giving surfactant to premature infants using a thin catheter at birth

  This study is testing if giving a special lung treatment to very premature babies right after birth using a thin tube can help them breathe better and need less breathing support in their first few days of life.

  Recruiting University College Dublin · Dublin, None Selected · NCT06557551

• Earlier use of an electric breast pump to maximize milk in preterm babies

  This study tests whether starting a double electric breast pump earlier (at birth) helps mothers of very preterm infants produce more milk by day 14.

  Recruiting National Maternity Hospital, Ireland · Dublin, Co. Dublin and 2 other locations · NCT07908238

• Adding azithromycin to ampicillin for late PPROM

  This test sees if adding a single dose of azithromycin to the usual ampicillin/amoxicillin treatment helps newborns when membranes break early between 34.0 and 36.6 weeks.

  Recruiting Phase 4 Sheba Medical Center · Ramat Gan, Israel · NCT07183462

• Medically tailored groceries to support pregnant people facing food insecurity

  This project will test whether home-delivered medically tailored groceries, with or without extra food education, help Medicaid-eligible pregnant people in Cuyahoga County improve nutrition and birth outcomes.

  Recruiting at 2 sites Case Western Reserve University · Cleveland, Ohio and 1 other locations · NCT06965530

• Tracking intellectual and motor development in babies at high risk for cerebral palsy

  This project will follow babies at higher risk for cerebral palsy to see if early thinking and movement signs predict later intellectual and motor outcomes.

  Recruiting at 3 sites University College Cork · Cork and 3 other locations · NCT06857539

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.