Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
75 participants
INTERVENTIONAL
2017-07-26
2022-03-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
NONE
Study Groups
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Control
This arm will consist of the usual care of management of hypertension by a clinical pharmacist.
Usual care
This intervention will consist of usual clinical care as determined by the clinical pharmacist.
Intervention
This arm will consistent of usual care plus the addition of a blood pressure cuff that will allow patients to upload data to the electronic health record via a secure portal.
Connected-device
This intervention will allow patients to upload blood pressure data automatically from a blood pressure cuff into the electronic health record.
Interventions
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Connected-device
This intervention will allow patients to upload blood pressure data automatically from a blood pressure cuff into the electronic health record.
Usual care
This intervention will consist of usual clinical care as determined by the clinical pharmacist.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Chronic kidney disease III or IV
* Systolic heart failure with ejection fraction \<35%
* Current use of 3 or more anti-hypertension drugs
18 Years
ALL
No
Sponsors
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Stanford University
OTHER
Responsible Party
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N. Lance Downing, MD
Clinical Assistant Professor of Medicine
Locations
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Stanford Primary Care
Portola Valley, California, United States
Stanford Primary Care Clinic
Santa Clara, California, United States
Countries
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Other Identifiers
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12397
Identifier Type: -
Identifier Source: org_study_id
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