Suspended
PRIMIPEREFirst-time Fathers' Experiences of Childbirth in Lorraine.
What is being collected
Data Collection
Collected from today forward - ProspectiveWho is being recruted
Over 18 Years
How is the trial designed
Case-Only
Examining characteristics of individuals with a disease in order to identify genetic or environmental factors contributing to the condition.Observational
Study Start: October 2020
Summary
Principal SponsorCentral Hospital, Nancy, France
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner
Study start date: October 12, 2020
Actual date on which the first participant was enrolled.The primary aim of this study is to evaluate first time father's experience during childbirth in three different maternity hospitals in Lorraine. Secondary aims of this study is to identify domains that need improvement in order to enhance fathers's experience during childbirth.
Official TitleFirst-time Fathers' Experiences of Childbirth in Lorraine.
Principal SponsorCentral Hospital, Nancy, France
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.Design Details
80 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Case-only
These studies focus only on individuals who have a specific disease. Researchers examine patterns—often genetic or environmental—to uncover what might be linked to the condition.
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Criteria
Male
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Inclusion Criteria: * First time father after a physiological pregnancy and delivery of a healthy newborn of more than 37 gestational weeks. Exclusion Criteria: \-
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Study Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Suspended
SuspendedOne Study Center