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NCT05546931Recruiting

Mobile Health Program for Rural Hypertension

Multilevel Mobile Health Program to Improve Rural Hypertension

Source: ClinicalTrials.gov · Last updated 19 Nov 2025

Brief summary (registry, in English)

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).

Status (registry)
Recruiting
Study type
Interventional
Enrollment
334 (estimated)
First submitted
15 Sept 2022
Start date
4 Sept 2023
Primary completion date
Dec 2026
Lead sponsor
University of Pittsburgh
NCT number
NCT05546931

What you commit to

  • Study type: Interventional
  • Planned participants: 334
  • From 4 Sept 2023 to the primary completion date, Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Heart failure necessitating hospital admission ≤3 months prior to study inclusion;
  • Acute coronary syndrome (defined as at least 2 of the following: chest pain, ischemic electrocardiographic changes, or troponin ≥0.1 ng/mL) ≤3 months prior to study inclusion;
  • Planned major surgery, cardiovascular or non-cardiovascular;

Other illness

  • Presence of non-cardiovascular conditions likely to be fatal within 12 months (e.g., cancer);

Other

  • Pregnancy or planned pregnancy within 12 months;
  • Inability to comprehend the study protocol, defined by failing 3 times to answer correctly a set of questions during consent;
  • Institutionalized status (e.g., nursing home, incarceration);
  • Inability to operate a smartphone or HBPM device due to sensory or neurocognitive deficit.

Who the study is looking for

  • History of uncontrolled hypertension, identified from the electronic health record problem list and an average systolic BP 140-199 or diastolic BP 90-119 mm Hg at 2 ambulatory visits, one of which is within 6 months of study entry
  • Residence in one of 48 counties categorized as rural by the Center for Rural Pennsylvania;
  • English-speaking at level appropriate for informed consent and study participation;
  • No plans to relocate from the area within 12 months of enrollment.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
University of Pittsburgh Medical Center
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PittsburghUnited StatesRecruiting

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.