Actively Recruiting
Home Blood Pressure Monitoring to Diagnose Hypertension in African American Adolescents
Led by University Hospitals Cleveland Medical Center · Updated on 2025-12-10
750
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating a new way to identify high blood pressure in African American adolescents, who are at higher risk for this condition. The study compares home blood pressure measurements, which have been used in Europe but not yet in the United States, to the best standard diagnostic method called 24-hour ambulatory blood pressure monitoring (ABPM). The goal is to understand if home monitoring can accurately detect high blood pressure in this higher-risk group of teens. Participants will use two types of devices: a home blood pressure machine to take readings twice daily for three consecutive days, and a 24-hour ambulatory blood pressure machine worn continuously for one day. These two methods will be compared to see how well home measurements agree with the 24-hour monitoring. Some teens and their parents will also be invited to participate in brief phone interviews about their experiences with both methods. During the study, teens will measure their blood pressure at home and wear the monitoring device for one full day. Researchers will count how many participants meet criteria for high blood pressure based on each method and measure the agreement between the two. They will also track how many complete both measurement protocols. The study involves up to two weeks of monitoring and follow-up, with safety and outcome evaluations conducted throughout the period.
CONDITIONS
Brief Title
Home BP Monitoring
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Self-identify or be identified by a parent as African American or partly African American
- Be between 13 and 18 years old
You will not qualify if you...
- Prior diagnosis of hypertension
- Currently prescribed blood pressure medication
- History of congenital heart disease
- History of solid organ transplant
- Regular use of stimulants or medications known to raise blood pressure such as testosterone or nicotine replacement
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 2 weeks
Participants use home blood pressure devices to measure their blood pressure as part of the trial procedures.
Participants measure blood pressure twice daily for three days and wear a 24-hour ambulatory blood pressure machine once
Trial Site Locations
Total: 1 location
1
University Hospitals Cleveland Medical Center
Cleveland, Ohio, United States, 44106
Actively Recruiting
Research Team
G
Goutham Rao, MD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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