NCT05763069Enrolling by invitation
HOME: Home Monitoring of High-risk Pregnancies
The HOME Study: Home Monitoring of High-risk Pregnancies
Source: ClinicalTrials.gov · Last updated 18 Feb 2026
Brief summary (registry, in English)
High-risk pregnancies often require long-term hospitalization or outpatient maternal and/or fetal monitoring, placing a burden on patients, hospital resources and society. The demand for intensified pregnancy surveillance and interventions is increasing, due to the increased prevalence of risk factors like obesity and advanced maternal age, as well as altered guidelines resulting in increasing labor induction rates.The main aims of the HOME study (Home monitoring of pregnancies at risk) are to assess if home monitoring of selected high-risk pregnancies for maternal and fetal wellbeing is feasible, safe (in a clinical trial), cost-efficient, and simultaneously empowers the users.
- Status (registry)
- Enrolling by invitation
- Study type
- Observational
- Enrollment
- 250 (estimated)
- First submitted
- 28 Feb 2023
- Start date
- 21 Nov 2022
- Primary completion date
- Sept 2035
- Lead sponsor
- Oslo University Hospital
- Diseases
- High blood pressure
- NCT number
- NCT05763069
What you commit to
- Study type: Observational
- Planned participants: 250
- From 21 Nov 2022 to the primary completion date, Sept 2035
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- Multiples (twins, triplets etc)
- Patient or fetus in immediate need for delivery
- Not understanding Norwegian
- Not mastering the technological aspects of home monitoring
- Long travel distance to Obstetric Department
Who the study is looking for
- Preeclampsia
- Gestational Hypertension
- Premature Preterm Rupture of Membranes
- High Risk Pregnancy
- Previous adverse obstetric outcomes
Age in the registry: 18 years to 50 years · Sex: Female · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Oslo University Hospital Coordinator of this site? Confirm its status | Oslo | Norway | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.