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Clinical Trials/ACTRN12622000091707
ACTRN12622000091707
Not yet recruiting
未知

Effect of a mobile health program optimised with artificial intelligence (My Intelligent Cardiac Assistant—MICArdiac) on Systolic Blood Pressure and other cardiovascular risk factors in adults with high blood pressure: a multi-centre randomised controlled trial

niversity of Sydney0 sites500 target enrollmentJanuary 24, 2022

Overview

Phase
未知
Intervention
Not specified
Conditions
Hypertension
Sponsor
niversity of Sydney
Enrollment
500
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 24, 2022
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Participants are eligible if they meet all 3 of the following criteria and have no exclusion criteria.
  • 1\.Adults 35 years and over
  • 2\.Own a compatible smartphone – iPhone 5 onwards (iOS 10 and higher) or Android (6\.0 and higher).
  • 3\.Uncontrolled hypertension/high blood pressure (1 of the following):
  • a)Known hypertension AND at least one recorded measure of SBP equal or above to 140mmHg and/or DBP equal or above to 90 mmHg in the last 12 months; OR
  • b)At least one recorded measure of SBP equal or above to 160mmHg and/or DBP equal or above to 100 mmHg in the last 12 months; OR
  • c)At least two recorded measures of SBP equal or above to 140mmHg and/or DBP equal or above to 90 mmHg in the last 12 months.

Exclusion Criteria

  • History of cardiovascular disease, including peripheral artery disease, heart failure, coronary heart disease, stroke
  • Have a pacemaker, defibrillator or other electrical implant not suited for use with provided wireless monitoring devices.
  • Unable to use wearable/wireless monitoring devices provided
  • Unable to complete the study procedures or follow\-up
  • Unable to understand sufficient written English to provide informed consent
  • Unable to provide informed consent
  • Any condition that in the opinion of the responsible physician or investigator renders the patient unsuitable for the study (e.g. severe disability or significant memory or behavioural disorder)

Outcomes

Primary Outcomes

Not specified

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