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

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.

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

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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