Quality of Information Provided During Antenatal Consultations
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorHospices Civils de Lyon
About this trial
The objective of this questionnaire study is to evaluate the concordance between the information provided to parents during antenatal consultations and their subsequent experiences following childbirth.
Eligibility criteria
Qualifiers
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
Disqualifiers
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
Trial design
Treatments tested in this trial
- Survey
Treatment groups
113 Participants
are divided into 1 treatment groupLocations
1Femme Mère Enfant Hospital (HFME)69500, Bron France
Sponsors and collaborators
Hospices Civils de Lyon
Lead sponsor
Source ClinicalTrials.gov