Methods and analyses: Both are multicentre, non- masked, parallel group, randomised controlled trials. Participants will be randomised to self- monitoring with telemonitoring or usual care. BUMP 1 will recruit a minimum of 2262 pregnant women at higher risk of pregnancy hypertension and BUMP 2 will recruit a minimum of 512 pregnant women with either gestational or chronic hypertension. The BUMP 1 primary outcome is the time to the first recording of raised BP by a healthcare professional. The BUMP 2 primary outcome is mean systolic BP between baseline and delivery recorded by healthcare professionals. Other outcomes will include maternal and perinatal outcomes, quality of life and adverse events. An economic evaluation of BP self- monitoring in addition to usual care compared with usual care alone will be assessed across both study populations within trial and with modelling to estimate long- term cost- effectiveness. A linked process evaluation will combine quantitative and qualitative data to examine how BP self- monitoring in pregnancy is implemented and accepted in both daily life and routine clinical practice.
Ethics and dissemination: The trials have been approved by a Research Ethics Committee (17/WM/0241) and relevant research authorities. They will be published in peer- reviewed journals and presented at national and international conferences. If shown to be effective, BP self- monitoring would be applicable to a large population of pregnant women.