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临床试验/ACTRN12622000091707
ACTRN12622000091707尚未招募未知

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 个研究点目标入组 500 人开始时间: 2022年1月24日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
入组人数
500

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Prevention
盲法
Blinded (masking used)

入排标准

年龄范围
35 Years 至 o limit(—)
性别
All

入选标准

  • 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.

排除标准

  • 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)

研究者

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