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Virtual Maternity Ward for women with pregnancy complications: pilot evaluation

Virtual Maternity Ward for women with pregnancy complications: pilot evaluation

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12625000976482
Acronym
VMW
Enrollment
50
Registered
2025-09-04
Start date
2025-10-21
Completion date
2026-02-28
Last updated
2025-09-08

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

Conditions

None listed

Brief summary

The Royal Hospital for Women (RHW) in Randwick is implementing a new model of maternity care for women with pregnancy complications such as: a diagnosis of gestational hypertension, threatened premature labour (TPL) and/or premature pre-labour rupture of membranes (PPROM) called ‘Virtual Maternity Ward’. Women who have traditionally required inpatient admission, will be offered the opportunity to be cared for at home by midwives and obstetricians from the RHW. The midwifery team will consult with women regularly and collaborate with obstetricians and escalate women’s care when required. The new model with combine a midwifery home visiting program and periodic outpatient visits to RHW. Models of this type are common in Europe and have been operating as standard care for up to 10 years. Examples include maternity units in Aarhus University Hospital and Copenhagen University Hospital, Denmark and Utrecht University Hospital The Netherlands - see Lancet publication: Bekker, M. N., Koster, M. P. H., Keusters, W. R., Ganzevoort, W., de Haan-Jebbink, J. M., Deurloo, K. L., Seeber, L., van der Ham, D. P., Zuithoff, N. P. A., Frederix, G. W. J., van den Heuvel, J. F. M., & Franx, A. (2023). Home telemonitoring versus hospital care in complicated pregnancies in the Netherlands: a randomised, controlled non-inferiority trial (HoTeL). The Lancet. Digital Health, 5(3), e116–e124. https://doi.org/10.1016/S2589-7500(22)00231-X This pilot evaluation study will evaluate the feasibility and acceptability of the Virtual Maternity Ward at RHW model to women, their partners, clinicians and managers. It will also pilot methods for a future evaluation of cost (hospital and individual levels) and carbon emissions. The study is fully funded by NSW Health, SPHERE and UTS and has been approved by the HRECs of SESLHD and UTS. Governance approval has been granted by the RHW.

Interventions

On October 7th 2025, the Royal Hospital for Women (RHW) in Randwick, NSW is launching a new model of maternity care called the 'Virtual Maternity Ward' (VMW) for women with pregnancy complications such as: a diagnosis of gestational hypertension, threatened premature labour (TPL), and/or premature pre-labour rupture of membranes (PPROM). Women who have traditionally required inpatient admission, will be offered the opportunity to be cared for at home by midwives and medical officers from the RH

On October 7th 2025, the Royal Hospital for Women (RHW) in Randwick, NSW is launching a new model of maternity care called the 'Virtual Maternity Ward' (VMW) for women with pregnancy complications such as: a diagnosis of gestational hypertension, threatened premature labour (TPL), and/or premature pre-labour rupture of membranes (PPROM). Women who have traditionally required inpatient admission, will be offered the opportunity to be cared for at home by midwives and medical officers from the RHW. The midwifery team will consult with women regularly and collaborate with medical officers and escalate women’s care when required. The new model will combine remote blood pressure monitoring, a midwifery home visiting program and periodic outpatient visits to RHW. A Virtual Maternity Ward Working Group was established at RHW in June 2024, membership of which includes a multidisciplinary group of clinicians, managers, researchers, digital health experts and women with the ‘lived’ experience of receiving complex pregnancy care. This study, the ‘Virtual Maternity Ward Pilot Evaluation’ will evaluate the model of care, in a cohort of women who have been admitted to the VMW and are being cared for at home (n=20), partners/support people (n=15-20), health service managers (n=3-5) and clinicians (5-10). Women and their partner participants will be recruited from those already admitted to the Virtual Maternity Ward by their treating clinician. Women participants will not be asked to participate in any procedures other than their standard course of treatment, as agreed to with their treating clinician. Hence, this study is OBSERVATIONAL only. The aim of the ‘Virtual Maternity Ward Pilot Evaluation’ is to evaluate the model of care from the perspectives of technical, financial, operational, and logistic feasibility, and to pilot test the methods to inform the refinement of the model and design of future larger studies. Data collected will include 1) semi structured interviews, 2) cost diaries and 3) data collected from medical records, all collected after participants' discharge from VMW. 1) Semi structured interviews will be conducted by a GCP trained research midwife/PhD Candidate who will ask women participants about their views and experiences of being cared for at home in the Virtual Maternity Ward. Interviews are expected to take 20-30 minutes and will be conducted via an online platform or phone, according to the participants’ preferences Semi structured interviews with clinicians and managers will be also conducted, after the last participant has been discharged from the VMW. The interview will ask clinicians about their views and experiences of providing care in the Virtual Maternity Ward model. Interviews are expected to take 20-30 minutes and will be conducted at RHW in a private space, or by phone, according to the participants’ preferences. 2) A pilot costing study will be included at both individual and hospital levels. To identify the costs of the Virtual Maternity Ward, payroll data identifying the salary costs of Virtual Maternity Ward and standard care midwives during the trial time will be extracted to identify amount of standard care midwife time required to deliver virtual episodes of care. To identify additional background health service use, electronic medical records will be extracted to identify participating women’s inpatient, outpatient and emergency department health service use from onset of antenatal care through to 6 weeks postpartum. We will also establish out of pocket costs for women through cost diaries. 3) Data extraction form medical records: • Routinely collected perinatal outcomes data – eMaternity o Demographic information including age, gestation at birth, parity, ethnicity o Reason for admission o Mode of birth – normal vaginal birth, emergency caesarean section, instrumental birth o Medical and obstetric history o Outpatient presentations to hospital o Admissions as inpatients to hospital o Length of admission to VMW o Apgar scores below 7 at 5 minutes o NICU admission of over 48 hours o Length of stay in hospital

Sponsors

University of Technology Sydney
Lead SponsorUniversity

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

Women: • Women who have been admitted to the ‘Virtual Maternity Ward’ by their treating clinician. • Willingness to provide written informed consent to participate in the research. For partners/support people: • Partners/family members or support people caring for participating women at home • Willingness to provide verbal informed consent For Clinicians: • Registered midwife or medical officer employed at the Royal Hospital for Women • Provided direct clinical care to women on the Virtual Maternity Ward • Willingness to provide verbal informed consent For Health Service Managers: • Health Service Managers at RHW who have responsibility for staff working in the Virtual Maternity Ward • Willingness to provide verbal informed consent

Exclusion criteria

For Women: • Women with a psychological illness or condition such as to interfere with her ability to understand the requirements of the study. • Women with a fetus known to be incompatible with life (as this clinical circumstance brings added burden to the woman, her family and caregivers and is beyond the scope of this study) No exclusion criteria for clinicians and managers who meet inclusion criteria.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026