Quality of Information Provided During Antenatal Consultations

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.

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Key information

Conditions

Congenital Anomalies Antenatal Consultation Congenital Abnormalities Congenital, Hereditary, and Neonatal Diseases and Abnormalities Female Urogenital Diseases and Pregnancy Complications Obstetric Labor Complications Obstetric Labor, Premature Pregnancy Complications Premature Birth Prematurity Urogenital Diseases

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

Femme Mère Enfant Hospital (HFME)

Bron, 69500, France

Location status: Recruiting

Location contact

Hélène GAUTHIER MOULINIER, MD

CONTACT

[email protected]

+33427855284

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Survey

Other

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 outcomes

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.

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'.

Study contacts

Contact information is provided by the study sponsor or research team.

Cosima BABINET

CONTACT

[email protected]

+33608161034

Sponsors and collaborators

Lead sponsor

Hospices Civils de Lyon

Other

Registry information

Official study title

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

Acronym: EVIDANCE

Important dates

Study start: 2024
Primary completion: 2025
Study completion: 2025
First posted: Feb 11, 2025
Registry last updated: Feb 11, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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