Patients' Choice of Health Care Provider for Monitoring Their Pregnancy (Grossesse-Cx)

Hôpital NOVO

Status: Completed

Conditions: Pregnancy Related

Treatments: Other: Patient questionnaire

Study type: Interventional

Funder types: Other

Identifiers

NCT05774353

CHRD0322

Details and patient eligibility

About

The aim of this study is to understand and interpret the determinants that lead pregnant women to refer more to a health professional in order to better meet the patient's request.

Full description

Pregnancy is a natural phenomenon that occurs without complication in the majority of pregnant women. Pregnancy monitoring is necessary to detect possible complications and improve the comfort and experience of all pregnant women. For several years now, pregnant women have wanted to benefit from pregnancy monitoring as well as a less medical and physiological delivery according to the perinatal plan 2005-2007.

Perinatal plans have been implemented and evaluated for over 30 years. Progress has been made in terms of obstetrical and perinatal safety. The latest plan advocates a "humanisation of birth" which leaves more room for the parents' wishes. Pregnancy monitoring is currently carried out by doctors or midwives as part of seven compulsory prenatal examinations. This medical follow-up is completed by a preparation for birth with group classes, based on these general and obstetrical assessments.

After declaring their pregnancy, women can consult various health professionals to monitor their pregnancy. The aim of this study is to understand and interpret the determinants that lead pregnant women to be more oriented towards one health professional or another. Each determinant will be analysed and quantified in order to better respond to patient demand. The investigator chose to interview women who had just given birth and not pregnant women because the health professional may change during the course of the pregnancy, and the investigator assumes that the women will have more perspective on their experience and their choice once they have given birth.

Enrollment: 400 patients

Sex: Female

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria :

• Woman in post-natal care at the NOVO hospital - Pontoise site
• Women aged 18 and over

Exclusion Criteria :

• Women who do not speak or understand French language (written and oral)
• Woman under legal protection (guardianship, curatorship...)
• Refusal to participate

Trial design

Primary purpose: Other

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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400 participants in 1 patient group

Patient questionnaire

Other group

Description:

Patients included in the study will complete an online questionnaire (LimeSurvey).

Treatment:

Other: Patient questionnaire