Blood Pressure Monitoring in High Risk Pregnancy to Improve the Detection and Monitoring of Hypertension
NCT03334149 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 3042
Last updated 2022-06-06
Summary
Raised blood pressure is a common problem in pregnancy. Raised blood pressure and pre-eclampsia affect about one in ten women and are a major cause of death and premature birth in the United Kingdom and worldwide.
Many women have expressed an interest in monitoring their own blood pressure in between antenatal visits but there has been very little research to guide this. The investigators would like to know if the diagnosis and subsequent care of women with raised blood pressure can be improved if women were able to monitor their own blood pressure safely at home. This work will test whether optimising the diagnosis, monitoring and management of raised BP during pregnancy through self-monitoring of BP is effective, acceptable and cost-effective compared to usual care.
The research team have being working with pregnant women, doctors and midwives to develop a simple and accurate method of self-monitoring of blood pressure in pregnancy.
This randomised controlled trial will:
1. Compare self-monitoring with usual care in women at higher risk of hypertension in pregnancy and assess if self-monitoring can identify raised blood pressure earlier.
2. Compare self-monitoring with usual care for women with high blood pressure in pregnancy to see if it leads to lower blood pressure.
3. Assess if self-monitoring is cost-effective.
Pregnant women who chose to take part in these studies will be randomised to either usual care or asked to monitor their own blood pressure during their pregnancy in addition to their usual antenatal care.
Conditions
- Pregnancy, High Risk
- Pre-Eclampsia
- Hypertension
- Hypertension, Pregnancy-Induced
Interventions
- OTHER
-
Self-Monitoring of Blood Pressure
BUMP 1: Women randomised to the self-monitoring arm will be asked to measure blood pressures at least three times a week. They will perform two readings with a one minute interval and will be asked to act on the second reading if it falls outside their normal range thresholds described in their instructions, and aided by the tele monitoring system. BUMP 2: Women randomised to the self-monitoring arm will be asked to measure blood pressures daily. They will perform two readings with a one minute interval and will be asked to act on the second reading if it falls outside their normal range thresholds described in their instructions, aided by a tele monitoring system.
Sponsors & Collaborators
- collaborator OTHER
-
Oxford University Hospitals NHS Trust
collaborator OTHER -
University of Southampton
collaborator OTHER -
University of Birmingham
collaborator OTHER -
Barts & The London NHS Trust
collaborator OTHER -
City, University of London
collaborator OTHER -
National Institute for Health Research, United Kingdom
collaborator OTHER_GOV -
University of Oxford
lead OTHER
Principal Investigators
-
Richard J McManus, PhD MBBS · University of Oxford
Study Design
- Allocation
- RANDOMIZED
- Purpose
- HEALTH_SERVICES_RESEARCH
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- FEMALE
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2017-11-22
- Primary Completion
- 2020-09-16
- Completion
- 2020-09-16
Countries
- United Kingdom
Study Locations
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