Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05546931

Mobile Health Program for Rural Hypertension

Led by University of Pittsburgh · Updated on 2025-11-19

334

Participants Needed

1

Research Sites

195 weeks

Total Duration

On this page

Sponsors

U

University of Pittsburgh

Lead Sponsor

N

National Heart, Lung, and Blood Institute (NHLBI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Hypertension (HTN) is the leading modifiable cause of cardiovascular disease. Rural individuals experience challenges of the rural health divide: geographic distance from providers, social isolation, limited social resources, and high rates of low health literacy. This study evaluates a home-based blood pressure monitoring (HBPM) program that provides longitudinal health education, empathic guidance, monitoring, and adaptable patient-centered coaching to rural individuals. Participants in this study will be randomized to receive (1) HBPM with the intervention; or (2) the control, consisting of HBPM and a smartphone with a general health application (WebMD).

CONDITIONS

Official Title

Mobile Health Program for Rural Hypertension

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • History of uncontrolled hypertension, with average systolic BP 140-199 or diastolic BP 90-119 mm Hg at 2 ambulatory visits, including one within 6 months before study entry
  • Residence in one of 48 counties classified as rural by the Center for Rural Pennsylvania
  • English-speaking at a level sufficient for informed consent and participation
  • No plans to move away from the area within 12 months after enrollment
Not Eligible

You will not qualify if you...

  • Heart failure requiring hospital admission within 3 months prior to study entry
  • Acute coronary syndrome within 3 months before study inclusion
  • Planned major surgery (cardiovascular or non-cardiovascular)
  • Pregnancy or plans to become pregnant within 12 months
  • Non-cardiovascular conditions likely to be fatal within 12 months (e.g., cancer)
  • Inability to understand the study protocol, failing consent questions 3 times
  • Institutionalized status such as nursing home residency or incarceration
  • Inability to use a smartphone or home blood pressure monitor due to sensory or neurocognitive problems

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Pittsburgh Medical Center

Pittsburgh, Pennsylvania, United States, 15213

Actively Recruiting

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Research Team

J

Jared W Magnani, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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