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Patient Satisfaction During Physiological Water or Land Birth: a Prospective Study in an French Tertiary Maternity Unit.

Patient Satisfaction With Physiological Childbirth in Water or on Land a Prospective Study at the Tourcoing Hospital Maternity Unit

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06441370
Acronym
AQUAMODA
Enrollment
1200
Registered
2024-06-04
Start date
2024-04-01
Completion date
2026-06-01
Last updated
2024-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Water Birth

Brief summary

A study will be carried out to compare the level of satisfaction and psychological state of women who give birth in water with those who give birth out of water. The aim is to demonstrate the benefits of water birth and justify its place in the healthcare offering.

Interventions

PROCEDUREwaterbirth

waterbirth: laboured for all or part of the first stage of labour and remained in the water for birth of newborn

Sponsors

Tourcoing Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Major patient * Social security beneficiary * Presence of a companion * Delivery greater than or equal to 37 weeks of amenorhoea * Spontaneous labor * Cephalic presentation * Physiological delivery by woman's choice according to 2017 HAS criteria (French recommendations)

Exclusion criteria

* Patient under court protection * Patient under guardianship or curatorship * Placement of an epidural * Language barrier * Unexpected delivery (unwanted by the woman) * Scarred uterus * Meconium fluid * Maternal pathologies: epilepsy, MS (depending on neurological opinion), diabetes (types 1 and 2), herpes infection, HIV, HBV, HCV * History of delivery hemorrhage \> 1L * History of shoulder dystocia/clavicle fracture * Metrorrhagia * Administration of nalbuphine within 2 hours of birth.

Design outcomes

Primary

MeasureTime frameDescription
Perceived control over childbirthThis questionnaire will be achieved by participating women within 3 days postpartum, before discharge from the maternity ward.The perception of control over childbirth dimension of the QEVA (Quality and Experience of Childbirth), a long version with a total of 6 dimensions. The score associated with the perception of control over childbirth dimension is obtained by averaging responses to items 8, 10, 11, 12, 14 and 18 of the questionnaire. The response to each of these items is coded on a Likert scale from 1 to 4, with a high value corresponding to poor control.

Secondary

MeasureTime frameDescription
Dimension of the quality and experience of childbirth within 3 days of deliveryThis questionnaire is to be completed within 3 days of delivery, before discharge from the maternity hospital.The scores associated with the 5 other dimensions of the QEVA questionnaire: * Expectations, defined by items 9, 15 and 20; * Sensory experience, defined by items 3 and 16; * Relationship with caregivers, defined by items 5, 6, 7 and 13; * Emotions, defined by items 1, 2, 4, 21, 22, 23 and 24; * First moments with baby, defined by items 17, 18 and 19; Answers to the questions are coded on Likert scales from 1 to 4. Each score is calculated by averaging the responses to the questions in the dimension in question.
Dimension of the quality and experience of childbirth within 2 months of deliveryThis questionnaire is to be completed within 2 months of delivery.The scores associated with the 5 other dimensions of the QEVA questionnaire: * Expectations, defined by items 9, 15 and 20; * Sensory experience, defined by items 3 and 16; * Relationship with caregivers, defined by items 5, 6, 7 and 13; * Emotions, defined by items 1, 2, 4, 21, 22, 23 and 24; * First moments with baby, defined by items 17, 18 and 19; Answers to the questions are coded on Likert scales from 1 to 4. Each score is calculated by averaging the responses to the questions in the dimension in question.
Anxiety and depression at 2 months of delivery.This questionnaire is to be completed within 2 months of delivery.The Edinburgh Postnatal Depression Scale (EPDS) will be used to assess anxiety and depression and depression at 2 months postpartum in order to screen for possible postpartum depression.

Countries

France

Contacts

Primary ContactVitagliano JV Jean-Jacques, PhD
jjvitagliano@ch-tourcoing.fr03.20.69.42.80
Backup ContactDegrendel MD Maxime, MD
mdegrendel@ch-tourcoing.fr03.20.69.42.80

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026