- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07263971
Birth Experience of Women Giving Birth in Belgium
December 1, 2025 updated by: Université Catholique de Louvain
Birth Experiences of Women Giving Birth in French-speaking Belgium and Pathways to Choosing a Place of Birth
The aim of this research is to understand what motivates women giving birth in Belgium to choose a particular place of birth and their experiences of childbirth.
This understanding is made possible by collecting qualitative data from women who have given birth (from the first month after giving birth up to one year postpartum).
The objective here is to understand what motivates the choice of place of birth (with a focus on the notion of 'non-choice') and to gain insight into the childbirth experiences of women giving birth in Belgium.
The researcher also meets with birth companions (perinatal health professionals and birth companions such as doulas, for example) to understand their professional practice and their choice of workplace (home, birth centre or cottage, traditional hospital ward, university hospital ward, etc.).
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
60
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Woluwe-Saint-Lambert
-
Brussels, Woluwe-Saint-Lambert, Belgium, 1200
- Recruiting
- UCLouvain
-
Contact:
- Céline Chomé, PhD student
- Phone Number: 027643635
- Email: celine.chome@uclouvain.be
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Women having given birth within a year
Description
Inclusion Criteria:
- have given birth in Belgium
- have given birth less than a year ago
- be of legal age
- volunteer
Exclusion Criteria:
- not having given birth once in Belgium
- being a minor
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Women who have given birth
Qualitative interviews with women who have given birth
|
Qualitative interview with volunteering women having given birth.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Birth experience
Time Frame: Throughout the entire study, approximately during 40 months
|
The outcome is how women have experience their delivery.
As it is through qualitative interviews, we can not yet specify the results.
|
Throughout the entire study, approximately during 40 months
|
|
Birthplace Choice
Time Frame: Throughout the entire study, approximately during 40 months
|
Which birthplace women have choosen, do they have the feeling they had a choice.
If yes : how women choose the birth place, when and what influenced them in their decision.
If not : who took the decision and why.
|
Throughout the entire study, approximately during 40 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 8, 2025
Primary Completion (Estimated)
December 31, 2028
Study Completion (Estimated)
December 31, 2028
Study Registration Dates
First Submitted
September 23, 2025
First Submitted That Met QC Criteria
December 1, 2025
First Posted (Estimated)
December 4, 2025
Study Record Updates
Last Update Posted (Estimated)
December 4, 2025
Last Update Submitted That Met QC Criteria
December 1, 2025
Last Verified
December 1, 2025
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- NAISSANCE
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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