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RECRUITING
NCT07523269
NA

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

Sponsor: Aktiia SA

View on ClinicalTrials.gov

Summary

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.

Key Details

Gender

All

Age Range

21 Years - 85 Years

Study Type

INTERVENTIONAL

Enrollment

164

Start Date

2026-04

Completion Date

2027-12

Last Updated

2026-04-13

Healthy Volunteers

No

Interventions

DEVICE

Aktiia G1 BP monitor for 12 months

These participants will receive an Aktiia G1 BP monitor and wear it through the entire 12-month study period.

DEVICE

Traditional BP monitor for 6 months / Aktiia G1 BP monitor for 6 months

These participants will receive a traditional BP monitor (validated upper arm cuff) to use for the 6 months comparison period. At the 6-month visit, they will return the traditional BP monitor and receive an Aktiia G1 BP monitor for the 6-month follow-up period.

Locations (1)

Mass General Brigham Hospital

Boston, Massachusetts, United States