Recruiting NCT06820892
Quality of Information Provided During Antenatal Consultations
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Survey.
- Who it may be relevant to
- Registry conditions: Congenital Anomalies, Prematurity, Antenatal Consultation. Basic parameters: from 18 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Evaluation of the Concordance Between the Information Delivered in Antenatal Diagnosis Consultation and Parents Experience After the Birth of Their Infant
Overview
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.
Interventions
- Other Survey
The study utilised a 16-item questionnaire to evaluate the quality of information received during antenatal diagnosis consultations and its congruence with subsequent experiences following birth and hospitalisation of the infant. The questionnaire encompassed seven questions pertaining to consultation arrangements, including duration, frequency and unit visits, six questions addressing the received information, and three questions exploring the long-term outcomes of the child.
Primary outcome measures
- Question 8 of the questionnaire [Time frame: The outcome is measured at the time of questionnaire completion, typically at hospital discharge or within one week post-discharge.]
Eligibility 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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Other
Study locations
France · 1 center
- Femme Mère Enfant Hospital (HFME) — Bron
Identifiers
NCT: NCT06820892 · 24-5216