Evaluating information given to parents during prenatal consultations
Evaluation of the Concordance Between the Information Delivered in Antenatal Diagnosis Consultation and Parents Experience After the Birth of Their Infant
This study is trying to see if the information parents get during prenatal visits matches their experiences after their baby is born, especially regarding issues like congenital anomalies and prematurity.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 113 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | Hospices Civils de Lyon Academic / other |
| Locations | 1 site (Bron) |
| Trial ID | NCT06820892 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates for this study are parents who attended antenatal consultations with a pediatric neonatologist and gave birth between January 2020 and December 2022.
Not a fit: Patients who may not benefit from this study include those whose newborns had a high risk of death or who were non-French speaking mothers.
Why it matters
Potential benefit: If successful, this study could enhance the quality of information provided to parents during antenatal consultations, leading to better preparedness and support for families.
How similar studies have performed: While there may be similar studies evaluating antenatal information, this specific approach focusing on post-birth experiences is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
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 this trial is running
Bron
- Femme Mère Enfant Hospital (HFME) — Bron, France (Recruiting)
Study contacts
- Study coordinator: Cosima BABINET
- Email: cosima.babinet@chu-lyon.fr
- Phone: +33608161034
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.