Wearable Evaluation of Ambulatory Readings for Blood Pressure
Stephen Juraschek
100 participants
Jun 6, 2025
INTERVENTIONAL
Conditions
Summary
The purpose of this project is to compare the performance and validity of novel wearable technologies that measure blood pressure (BP) and physical activity with a Spacelabs Ambulatory Blood Pressure Monitoring (ABPM) device.
Eligibility
Inclusion Criteria5
- Age 18 to 100 years
- All neighborhoods in Boston area
- Be able to walk with two limbs and have two arms
- Willing and able to complete required measurement procedures
- Able to provide informed consent
Exclusion Criteria2
- Failure to receive informed consent
- Arm circumference of more than 50cm
Interventions
This is an upper arm, cuff-based intermittent ambulatory BP device. This device has an internal activity and body position sensor which gathers information about sleep-wake estimation.
This is an upper arm cuff-based device with tubing for continuous ambulatory BP monitoring with a unique activity sensor that correlate with patient movement activity with blood pressure changes.
This is a wrist cuff-based device which uses an optical sensor (photoplethysmography sensor) to gather data from the arteries under the skin surface. Aktiia has an upper arm cuff device which is used for calibration once every month to provide a baseline blood pressure reading.
This is a wrist cuff-based applanation tonometry continuous ambulatory BP device. This device has automatic self-calibration and comes in various sizes.
This is a wrist cuff-based wireless oscillometric, continuous ambulatory BP device. It has applanation tonometry at the wrist with Pulse wave analysis. This device needs calibration with a brachial cuff BP measurement.
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT06610448