Status:

RECRUITING

Collaboration Oriented Approach to Controlling High Blood Pressure

Lead Sponsor:

Oregon Health and Science University

Collaborating Sponsors:

University of Missouri-Columbia

Vanderbilt University Medical Center

Conditions:

Hypertension

Multiple Chronic Conditions

Eligibility:

All Genders

18-100 years

Phase:

NA

Brief Summary

Hypertension is a significant contributor to poor cardiovascular outcomes. Self-management support tools can increase patient behaviors to improve blood pressure. The investigators created a clinical ...

Detailed Description

This protocol addresses the challenge of implementing scalable, interoperable clinical decision support (CDS) and the patient-centered outcome of avoiding heart attacks and strokes through high blood ...

Eligibility Criteria

Inclusion

  • Adult patients aged 18-100 years old
  • Patient receives care at a participating primary care clinic and has been seen in the last year
  • Patient has high BP, defined as an average of 4 BPs \> 140 systolic or \> 90 diastolic (clinic) or \> 135 OR \> 85 (home)
  • Patient is enrolled in online health portal
  • Patient can communicate in English
  • Patient has been recommended by their physician who thinks the patient would benefit from a home blood pressure monitoring program.

Exclusion

  • Patient is pregnant at the time of consent
  • Patient who, in the opinion of the primary care clinician, has severe cognitive impairment
  • Patient is on hospice care and/or has a life expectancy of less than 2 years
  • Patient has end stage renal disease
  • Patient for whom tight blood pressure control presents a greater risk, such as those with a history of adverse events from hypertension treatment (falls, dizziness, electrolyte disturbances, hypotension, active heart failure)
  • Patient has any other disease or disorder that in the opinion of the investigator or the patient's primary care clinician, could put participants at risk and affect trial results, or hinder participation will exclude them from participating

Key Trial Info

Start Date :

January 12 2024

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

June 30 2026

Estimated Enrollment :

550 Patients enrolled

Trial Details

Trial ID

NCT06124716

Start Date

January 12 2024

End Date

June 30 2026

Last Update

April 11 2025

Active Locations (3)

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Page 1 of 1 (3 locations)

1

University of Missouri-Columbia

Columbia, Missouri, United States, 65211

2

Oregon Health & Science University

Portland, Oregon, United States, 97239

3

Vanderbilt University Medical Center

Nashville, Tennessee, United States, 37232