Quality of Information Provided During Antenatal Consultations
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorHospices Civils de Lyon
About this trial
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
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
Disqualifiers
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
Trial population
Of the patients who were followed up at the multidisciplinary prenatal diagnosis centre and had an antenatal consultation with a pediatric neonatologist, 113 patients met the inclusion criteria.
Trial design
Design model
Other
Time perspective
Retrospective
Treatments tested in this trial
Survey
Other interventionThe 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.
Treatment groups
113 Participants
are divided into 1 treatment groupGroup A: Patients (mother only)1 intervention
Trial outcomes
Primary outcomes
1
Question 8 of the questionnaire
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'.
Time frame
The outcome is measured at the time of questionnaire completion, typically at hospital discharge or within one week post-discharge.Sponsors and contacts
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Source ClinicalTrials.gov