WEARABLE-BP: Wearable Everyday Automated Readings to Enable Assessment of Blood Pressure Control

The WEARABLE-BP study will evaluate the clinical value of obtaining continual measurements using the Aktiia G1 Optical Blood Pressure Monitoring (OBPM) device in hypertensive patients, compared to using a traditional upper arm cuff for home BP monitoring. The WEARABLE-BP study aims to compare the change in unattended automated office blood pressure from baseline to 6 months between two study groups: those given an Aktiia G1 BP monitor and those given a traditional upper arm BP cuff.

NCT Number	NCT07523269
Lead Sponsor	Aktiia SA Collaborators: Massachusetts General Hospital, Brigham and Women's Hospital
Conditions	Hypertension (HTN)
Enrollment	164 participants
Start Date	2026-04
Primary Completion	2027-09 (estimated)
Study Completion	2027-12 (estimated)
Updated on ClinicalTrials.gov	2026-04-13