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OpenTrials
Completed

NCT Number: NCT06078540

A Mobile Health (mHealth) Strategy for Improving Blood Pressure Control Among Adult Hypertensive African Americans

The purpose of this study is to test the proof-of-concept for adding a novel mHealth application, USeeBP, to the established UChicago Medicine Ambulatory Medicine Remote-Patient Monitoring (UCM-RPM) Hypertension Management Program in a population of African American adults with poorly controlled hypertension.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Chicago

Chicago, Illinois, 60637, United States

About this study

This is a single-arm, proof of concept study, which we will use to assess for initial evidence of efficacy and technical feasibility of adding the USeeBP mHealth app as an adjunct to the UCM-RPM program.

This study integrates the USeeBP app into the existing UCM-RPM clinical pathway. Regular UCM-RPM program activities include monitoring home blood pressure (BP) measurement flowsheets, performing patient telephone and EPIC MyChart message outreach, and making medication adjustments. USeeBP is a secure, chat-based smartphone application. The app connects to a patient's electronic BP cuff (eCuff) via Bluetooth and sends BP data to the UCM-RPM program (rather than using the companion app to the eCuff that is used in the UCM-RPM program). The USeeBP app also allows the patient to set BP check and medication reminders, as well as provides patient education and opportunities to participate in healthy behavior challenges.

The primary study goal is to measure the effect of the USeeBP mobile app on home BP. Serial home blood pressure measurements will be collected at multiple time points. We hypothesize that there will be a decrease in BP across the study period.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • African American
  • Ages 18 to 65 years old
  • Able to demonstrate English reading literacy of at least 8th grade level [Rapid Estimate of Adult Literacy in Medicine, Revised (REALM-R) score ≥ 6]
  • Prior hypertension (HTN) diagnosis
  • Clinically measured SBP ≥ 160 mmHg recorded during at least 2 of last 4 encounters within past 2 years
  • UCM-RPM Hypertension Management Program current or eligible participant
  • Access to an Android or Apple iOS smartphone and its corresponding health app
  • Access to an active data plan or home Wi-Fi
  • Willing to use wireless electronic blood pressure cuff (eCuff)
  • Has access to EPIC myChart mobile app or is willing to establish myChart account and download app
  • Willing to download USeeBP study app to phone
  • Willing to download and use USeeBP app with staff assistance

Exclusion criteria

  • Hypertension is managed by a specialist (specialist prescribes the anti-hypertensive therapies)
  • Baseline blood pressure greater than 180/110
  • Prior enrollment in the study
  • Known pregnancy
  • Prisoners
  • Active opioid dependency
  • Homelessness
  • Psychiatric hospitalization in the last year
  • Serious existing medical conditions that may make BP control difficult or necessitate frequent hospitalization (cirrhosis or hepatic failure, stage IV or V chronic kidney disease, interstitial nephritis, pulmonary arterial hypertension, right heart failure, history of dementia or neurocognitive disability, advanced heart failure, organ transplant, immunosuppressive therapy, active cancer treatment, patients on hospice care), stroke or myocardial infarction in past 90 days, severe aortic stenosis
  • Hospital admission for primary diagnosis of hypertensive emergency, hypertensive urgency, or uncontrolled hypertension in the past 90 days

Treatment and study plan

USeeBP

Other

USeeBP is a low risk mobile medical app that proposes to do no more than:

  • Help patients (i.e., users) self-manage their disease or conditions without providing specific treatment or treatment suggestions;
  • Provide patients with simple tools to organize and track their health information;
  • Provide easy access to information related to patients' health conditions or treatments;
  • Help patients document, show, or communicate potential medical conditions to health care providers;

Primary outcomes

  1. Change in home BP

    Time frame: Baseline, Week 12

    systolic pressure over diastolic pressure; measured by Bluetooth enabled, electronic, at home BP cuff

Secondary outcomes

  1. Change in BP control rate

    Time frame: Baseline, Week 12

    measured by clinical BP cuff, BP control defined as clinically-measured BP < 140/90 mmHg

  2. Change in medication adherence

    Time frame: Baseline, Week 12

    measured by Medication Adherence Report Scale (MARS-5); minimum value is 5, maximum value is 25; lower values indicate worse medication adherence

  3. Number of EPIC myChart patient-provider messages and replies

    Time frame: Week 12

    total number of messages and replies

  4. Number of hypertension related unscheduled emergency department or urgent care visits

    Time frame: Week 12

    total number of visits

Sponsors and collaborators

Lead sponsor

University of Chicago

Other

Registry information

Important dates

Study start
2023
Primary completion
2025
Study completion
2025
First posted
Oct 12, 2023
Registry last updated
Mar 3, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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