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临床试验/NL-OMON53577
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

发起方
Maasstadziekenhuis

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