- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07425665
Experiences of Early Postnatal Discharge Home as Perceived by Mothers and Healthcare Professionals (BbDom94)
Expériences du Retour à Domicile Post-natal précoce Par Les mères et Les Professionnels de santé : enquête Qualitative Sur Les Pratiques et Besoins
In recent years, the average length of stay in maternity units has decreased, leading to the development of early postnatal discharge home (EPDH) programs. Postnatal follow-up is a major public health issue, as it supports the physical and psychological well-being of mothers and newborns, helps parents adjust to their new roles, and promotes health prevention and education.
International studies show that mothers expect longer and more comprehensive follow-up, particularly regarding child development, sexuality, contraception, and returning to work. In France, EPDH has existed since the early 2000s and is offered to low-risk mothers and newborns shortly after birth, with two or three follow-up visits at home or in healthcare facilities.
As these programs are expected to expand, there is a need to better understand the experiences and needs of both mothers and healthcare professionals. This qualitative study, conducted in the Val-de-Marne department, aims to explore how they experience early discharge at individual, organizational, and medical levels. It seeks to identify the factors that contribute to positive or negative postnatal experiences and to compare local findings with existing international research.
Study Overview
Status
Conditions
Detailed Description
In recent years, the average length of stay in maternity units has decreased, and various early postnatal discharge home programs have been implemented. From a public health perspective, postnatal follow-up involves multiple challenges: it helps ensure the physical and psychological well-being of both mother and child and provides parents with support in caring for their newborn. During a period of vulnerability, it supports parents in their new roles while also contributing to health promotion and prevention (health behaviors, intra-family violence, etc.).
At the international level, several studies have identified the expectations of mothers and parents, who report a need for longer follow-up focused on child development, sexuality, contraception, and return to work.
In France, early postnatal discharge home (EPDH) has existed since the early 2000s. It is offered to low-risk women and newborns (as defined by the French National Authority for Health), two days after a vaginal birth and three days after a cesarean section. The program includes two or three follow-up visits, either at home or in a healthcare setting.
Early postnatal discharge programs are expected to expand as part of the reorganization of peri- and postnatal care, which requires the development of community-based services enabling mothers to access healthcare professionals as close as possible to their homes. This entails gaining a better understanding of the actual needs of mothers and healthcare professionals across different regions, which are characterized by considerable diversity.
This study is conducted in order to document the needs of mothers and healthcare professionals who experience early postnatal discharge home (EPDH) in the Val-de-Marne department.
It is a qualitative study that does not aim to test a hypothesis, but rather to document lived experiences in order to propose explanatory hypotheses. Accordingly, the study is grounded in the following research questions:
- How do healthcare professionals and mothers experience early postnatal discharge home in Val-de-Marne, at the individual, collective, organizational, familial, and medical levels, among others?
- According to them, what are the dimensions of a positive or negative postnatal experience? What are their needs and expectations?
- Do the experiences of mothers and healthcare professionals (as documented in this study) overlap with those identified in the predominantly international literature, or do they differ?
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Andrès IRURETA GOYENA CADIOT, Paramedical
- Phone Number: 0157023555
- Email: andres.iruretagoyenacadiot@chicreteil.fr
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Selection of Maternity
Inclusion Criteria:
- Public maternity unit in Val-de-Marne offering mothers early discharge home and willing to participate
Exclusion Criteria:
- Maternity unit opposed to participation
Selection of Home Care Professionals
Inclusion Criteria:
-Healthcare professional involved in the follow-up of early postnatal discharge home for women in Val-de-Marne and willing to participate in the study
Inclusion Criteria:
-Person with expertise in early return home and willing to participate
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The results of the thematic data analysis (see above "Data Analysis").
Time Frame: Eight months
|
The study triangulates sources by collecting observations, individual interviews, and group interviews.
All collected data are analyzed thematically and inductively, meaning that themes are developed dynamically by the researchers.
The analysis is conducted by two researchers and regularly discussed with the scientific committee
|
Eight months
|
Collaborators and Investigators
Investigators
- Principal Investigator: Edouard LECARPENTIER, Pr, Centre Intercommunal de Créteil
- Principal Investigator: Emmanuelle LAUMONDE, Midwife, Hôpitaux Paris Est Val-de-Marne (Site Saint-Maurice)
- Principal Investigator: Fabienne PIGEARD, Midwife, Centre Intercommunal de Villeneuve-Saint-George
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- BbDom94
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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