Actively Recruiting
Implementation of Intensive Hypertension Management Approaches: Cleveland Clinic
Led by Anita Misra-Hebert · Updated on 2026-01-09
1520
Participants Needed
1
Research Sites
181 weeks
Total Duration
On this page
Sponsors
A
Anita Misra-Hebert
Lead Sponsor
P
Patient-Centered Outcomes Research Institute
Collaborating Sponsor
AI-Summary
What this Trial Is About
The primary objective of the Implementation of Effective Hypertension Management Approaches: Cleveland Clinic program is to improve blood pressure control for patients diagnosed with hypertension (HTN) and uncontrolled blood pressure, specifically defined as a blood pressure greater than 150/95, across all Cleveland Clinic Northeast Ohio primary care practices. The project will scale up the availability of resources for treating hypertension in 56 primary care practices within the Cleveland Clinic Health System in Northern Ohio, reaching up to approximately 3800 patients. This project will utilize evidence from a randomized controlled trial by Margolis et al.(1) to build upon Cleveland Clinic's existing team-based primary care provider (PCP) collaboration with pharmacists and advanced practice providers (APP) and will use a mechanism that allows titrating blood pressure medications based on patient-recorded home blood pressure readings.
CONDITIONS
Official Title
Implementation of Intensive Hypertension Management Approaches: Cleveland Clinic
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Hypertension diagnosis, aged 18-85 years old
- Uncontrolled blood pressure, defined as a blood pressure reading of > 150/95
You will not qualify if you...
- Pregnant
- Stage 5 chronic kidney disease
- End Stage Renal Disease
- Enrolled in hospice care
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Cleveland Clinic
Cleveland, Ohio, United States, 44195
Actively Recruiting
Research Team
A
Anita Misra-Hebert, MD, MPH, FACP
CONTACT
C
Christopher Babuich, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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