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Clinical Trial Summary

In this RCT, up to 100 adults classified as pre-hypertensive will be randomized to either an artificial intelligence (AI) based lifestyle intervention group or an active control group with a 1 to 1 ratio. Both groups will receive an identical activity tracker (Samsung Galaxy Watch) and BP monitor (Omron Evolv). The AI intervention group will receive automated and personalized lifestyle recommendations based on their lifestyle (e.g. sleep, exercise and diet) and blood pressure (BP) data, involving an automated analytics engine using statistics and machine learning. The active control group will not receive these lifestyle recommendations. The investigators aim to assess objectively the effectiveness of the AI-based personalized lifestyle recommendations on the patients BP.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04543656
Study type Interventional
Source University of California, San Diego
Contact Sujit Dey, PhD
Phone 8587617518
Email dey@eng.ucsd.edu
Status Recruiting
Phase N/A
Start date October 1, 2020
Completion date June 2022

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