Actively Recruiting

Phase Not Applicable
Age: 13Years - 18Years
All Genders
Healthy Volunteers
ID05552547

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

Age: 13Years - 18Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Implementation

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

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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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