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Quality of Information Provided During Antenatal Consultations

Evaluation of the Concordance Between the Information Delivered in Antenatal Diagnosis Consultation and Parents Experience After the Birth of Their Infant

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06820892
Acronym
EVIDANCE
Enrollment
113
Registered
2025-02-11
Start date
2024-08-02
Completion date
2025-03-15
Last updated
2025-02-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Antenatal Consultation, Congenital Anomalies, Prematurity

Keywords

Antenatal, Antenatal consultation, information

Brief summary

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

OTHERSurvey

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.

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Question 8 of the questionnaireThe outcome is measured at the time of questionnaire completion, typically at hospital discharge or within one week post-discharge.In summary, did the information provided during the consultation with the paediatrician correspond to the events that transpired during your child's hospitalisation ? Patients are invited to indicate their level of agreement or disagreement with a series of four statements by selecting one of four options : 'not at all', 'to some extent', 'almost' or 'completely'.

Countries

France

Contacts

Primary ContactCosima BABINET
cosima.babinet@chu-lyon.fr+33608161034

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026