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
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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