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The water birth versus land birth study for pregnant women at low-risk of complications

Water birth Access at Term to Estimate Risks and Benefits In Research cohorTs in Hospital (WATERBIRTH): prospective cohort feasibility study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12616000973415
Acronym
WATERBIRTH
Enrollment
600
Registered
2016-07-25
Start date
2014-10-02
Completion date
2016-10-01
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

Water birth occurs when a baby is born fully submerged in water. There is a lack of strong (Level 1) evidence to conclusively agree on the safety or risk of water birth. We aim to determine if it is possible to run a large study that examines the safety of water birth compared to land birth in women with low-risk pregnancies. In this study, we will test recruitment parameters, research processes, and outcome measures (for mother and baby) to assess the feasibility of a main study. If this study proves feasible and funding is obtained, then we will consider an international study across multiple sites (subject to ethical approval) with the primary purpose of testing safety for babies who are born under water.

Interventions

Participants who intend to have a water birth on admission to birth suite will be allocated to a room with water birth facilities and have one-to-one care in labour by a midwife who is credentialed to conduct water births in accordance with evidence-informed guidelines. Women may access water immersion in labour and in the absence of an indication to exit the pool; the woman will proceed to give birth under water.

Sponsors

Professor Sue Kildea
Lead SponsorIndividual

Eligibility

Sex/Gender
All
Age
15 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

- 15 years or older - do not require interpreter - weigh less than 100 kilograms - low obstetric risk - suitable for intermittent auscultation in labour - singleton viable pregnancy - admitted to birth suite in spontaneous labour at term - vertex presentation - intact membranes or draining clear liquor (PROM <24 hours) - maternal and fetal observations within normal limits - vaginal bleeding within normal limits (i.e. no more than a 'show')

Exclusion criteria

- 14 years or younger - require an interpreter or legal guardian for consent - weigh 100 kilograms or more - obstetric risk factors - not suitable for intermittent auscultation in labour - multiple pregnancy or fetal demise - blood born infection e.g. Hepatitis B, C and HIV - major congenital anomalies - admitted to birth suite in labour <37+0 or >42 weeks' gestation - induction or planned caesarean - non-vertex presentation - meconium-stained liquor - abnormal maternal or fetal observations - any suspected or proven active infectious illness - requesting narcotic or epidural analgesia - any contraindication to intermittent fetal heart rate monitoring - vaginal bleeding more than 'show'

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026