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

Not Applicable
Recruiting
Conditions
Blood Pressure
Hypertension
Interventions
Other: USeeBP
Registration Number
NCT06078540
Lead Sponsor
University of Chicago
Brief Summary

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.

Detailed Description

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.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
30
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
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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
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
USeeBPUSeeBPParticipants will be asked to use the USeeBP mHealth app alongside participating in UCM-RPM program as part of their routine care.
Primary Outcome Measures
NameTimeMethod
Change in home BPBaseline, Week 12

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

Secondary Outcome Measures
NameTimeMethod
Number of hypertension related unscheduled emergency department or urgent care visitsWeek 12

total number of visits

Number of EPIC myChart patient-provider messages and repliesWeek 12

total number of messages and replies

Change in BP control rateBaseline, Week 12

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

Change in medication adherenceBaseline, Week 12

measured by Morisky Medication Adherence Scale \[Morisky Scale (MMAS-8)\]; minimum value is 0, maximum value is 8; lower values indicate worse medication adherence

Trial Locations

Locations (1)

University of Chicago

🇺🇸

Chicago, Illinois, United States

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