Telemonitoring and E-Coaching in Hypertensio
- Conditions
- Elevated Blood Pressure10057166
- Registration Number
- NL-OMON53577
- Lead Sponsor
- Maasstadziekenhuis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 400
- 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
- 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)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>- Proportion of patients with adequately controlled blood pressure (<140/90) at<br /><br>6 months</p><br>
- Secondary Outcome Measures
Name Time Method