Actively Recruiting

Age: 18Years +
FEMALE
ID06820892

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

Led by Hospices Civils de Lyon · Updated on 2025-02-11

113

Participants Needed

1

Research Sites

2 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to assess how well the information given to parents during antenatal consultations matches their actual experiences after childbirth. It focuses on mothers who attended a multidisciplinary prenatal diagnosis center and delivered newborns admitted to the hospital's neonatology department between January 2020 and December 2022. The study is observational and evaluates the quality and consistency of information provided during these consultations. Participants in this study completed a 16-item questionnaire that asked about various aspects of their antenatal consultations, including the number and length of visits, the information they received, and the long-term outcomes for their child. This survey was designed to capture the parents' views on the consultation process and their subsequent experiences after birth and hospitalization. Mothers answer questions mostly at the time of hospital discharge or within one week after leaving the hospital. Researchers analyze responses to understand how well initial information corresponds to postnatal reality. The primary outcome focuses on a specific questionnaire item reflecting this concordance. The study involves mothers only, with no additional treatments or interventions, and participation is based on completing the survey and providing feedback about their antenatal care experience.

CONDITIONS

Brief Title

Quality of Information Provided During Antenatal Consultations

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • 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
  • Female patients aged 18 years or older
Not Eligible

You will not qualify if you...

  • 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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Monitoring

Duration - From antenatal consultation through hospital discharge and up to one week post-discharge

Participants who attended antenatal consultations and delivered newborns hospitalized in the neonatology department are observed regarding the quality of information received during consultations and their experiences after birth.

1 visit at hospital discharge or within one week post-discharge

Trial Site Locations

Total: 1 location

1

Femme Mère Enfant Hospital (HFME)

Bron, France, 69500

Actively Recruiting

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Research Team

C

Cosima BABINET

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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