OBPM_HARMONY: Physiological Data Recording Over 24 Hours Using the Continual Optical Hilo Blood Pressure Monitor and an Ambulatory Blood Pressure Monitor

ConditionHypertension
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age21-85
SponsorAktiia SA

About this trial

The OBPM\_HARMONY study will enroll a minimum of 300 participants at the CHUV site in Lausanne, Switzerland. Each participant will complete two study visits at CHUV, scheduled at least 24.5 hours apart. Between these visits, participants will be asked to wear both the Hilo band, an Ambulatory Blood Pressure Monitor (ABPM) as well as a hydrostatic pressure system continuously for a 24-hour period.

Eligibility criteria

Qualifiers

Subjects aged 21 to 85yo

Subjects fluent in written and spoken French, capable of discernment

Subjects agreeing to attend the two study visits and follow study procedures

Subjects residing within 100 km of the CHUV site

Disqualifiers

Damaged/injured skin at the right wrist

Subjects with tachycardia (heart rate at rest > 120bpm)

Subjects with atrial fibrillation

Subjects with diabetes

Trial design

Treatments tested in this trial

  • Wearing Hilo band, Ambulatory Blood Pressure Monitor, and Hydrostatic Pressure monitor

Treatment groups

330 Participants
are divided into 1 treatment group

Locations

This trial has no locations

Sponsors and collaborators