Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
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
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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