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Home BP Monitoring

Home BP Monitoring for Diagnosis of Hypertension in African American Adolescents

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05552547
Enrollment
750
Registered
2022-09-23
Start date
2023-10-01
Completion date
2026-09-30
Last updated
2025-12-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

High Blood Pressure

Keywords

African American Teen, Home blood pressure monitoring

Brief summary

Most cases of high blood pressure in teens are missed for a number of reasons. One reason is that the most common way to make a diagnosis is to make three or more blood pressure measurements in a doctor's office on separate days. This can be inconvenient. Also, measuring blood pressure in the office might be inaccurate, since children (including teens) might have high values in the office but normal values at home. For these reasons, investigators wish to study a different way to identify teens with high blood pressure. Home BP measurements have been used in Europe to make a diagnosis, but not yet in the United States, and never in a higher risk population of teens. African American teens are at higher risk for high blood pressure than other teens. Investigators will compare the values received from the home BP machines to another method (24 hour ambulatory BP monitoring or ABPM) which is the best standard for diagnosis. Investigators also want to learn more about participants experience and their child's experience with both methods. A small sample of participating teens and parents will be invited to participate in short telephone interviews. This study plans to enroll a total of 750 teens at UH. Recruitment will not take place from other organizations.

Interventions

DEVICEHome Blood Pressure Machine

Participants will be asked to measure blood pressure twice daily for three days in a row at home.

DEVICE24-Hour Blood Pressure Machine

Participants will be asked to wear the machine for 24 hours.

Sponsors

University Hospitals Cleveland Medical Center
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
13 Years to 18 Years
Healthy volunteers
Yes

Inclusion criteria

* Self-identify or identified by a parent as African-American or of partly African American ancestry

Exclusion criteria

* Prior hypertension diagnosis * Prescribed BP medication * History of congenital heart disease * History of solid organ transplant * Prescribed and using stimulants and other medications on a regular basis known to raise blood pressure such as testosterone and nicotine replacement

Design outcomes

Primary

MeasureTime frame
Number of participants who meet criteria for hypertension based on 24-hour ambulatory BP reading.Up to 24 hours
True positive rate -- Number of home bp positives over ABPM positivesUp to 2 weeks
True negative rate -- Number of home bp negatives over ABPM negativesUp to 2 weeks
Number of participants who meet criteria for hypertension based on average home BP reading.Up to 2 weeks
Percent agreement between home BP-reading based diagnosis versus 24-hour ABPMUp to 2 weeks

Secondary

MeasureTime frame
Number of subjects who complete both home BP verus 24-hour ABPM protocolsUp to 3 weeks
Number of subjects who complete home BP protocolUp to 2 weeks

Countries

United States

Contacts

Primary ContactGoutham Rao, MD
goutham.rao@uhhospitals.org(216)844-3791

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026