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

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

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06078540
Enrollment
31
Registered
2023-10-12
Start date
2023-10-27
Completion date
2025-07-05
Last updated
2026-03-03

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

Conditions

Blood Pressure, Hypertension

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.

Interventions

OTHERUSeeBP

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;

Sponsors

University of Chicago
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Change in home BPBaseline, Week 12systolic pressure over diastolic pressure; measured by Bluetooth enabled, electronic, at home BP cuff

Secondary

MeasureTime frameDescription
Change in BP control rateBaseline, Week 12measured by clinical BP cuff, BP control defined as clinically-measured BP \< 140/90 mmHg
Change in medication adherenceBaseline, Week 12measured by Medication Adherence Report Scale (MARS-5); minimum value is 5, maximum value is 25; lower values indicate worse medication adherence
Number of EPIC myChart patient-provider messages and repliesWeek 12total number of messages and replies
Number of hypertension related unscheduled emergency department or urgent care visitsWeek 12total number of visits

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORDavid G. Beiser, MD

University of Chicago

Outcome results

None listed

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