NL-OMON53577招募中不适用
Telemonitoring and E-Coaching in Hypertension - TECH
Maasstadziekenhuis0 个研究点目标入组 400 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 400
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 64(—)
入选标准
- •- Patients >18 years with hypertension (>140/90) will be included after their
- •emergency department or outpatient clinic visit. - Have and use a smartphone or
- •a partner/caregiver who is able to provide the necessary technical support -
- •Able to provide written informed consent prior to participation in the study
排除标准
- •- Current user of the iHealth Track blood pressure monitor and Luscii app -
- •Persistent atrial fibrillation as indicated in the electronic health record
- •(EHR) - Pregnant or planning to become pregnant during the study period -
- •Severe kidney disease, defined as estimated glomerular filtration rate <30 per
- •1.73 m2 or currently on renal replacement therapy (i.e. hemodialysis or
- •peritoneal dialysis) - Unable to communicate (not language specific) - History
- •of a cardiovascular event (ischemic stroke, transient ischemic attack,
- •myocardial infarction, coronary artery bypass grafting) in the past 3 months -
- •Diagnosis of dementia, psychosis as indicated in the electronic health record -
- •Life expectancy <1 year (eg Terminal cancer diagnosis or NYHA III or IV heart
- •failure) - Individuals requiring BP monitor cuff size larger than 42cm -
- •Patients with very obvious clinical clues for a secondary cause of their
- •hypertension (e.g. excessive licorice use, proven renal artery stenosis etc)
研究者
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