Hypertension Clinical Trial
Official title:
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.
Status | Recruiting |
Enrollment | 30 |
Est. completion date | October 2024 |
Est. primary completion date | October 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
United States | University of Chicago | Chicago | Illinois |
Lead Sponsor | Collaborator |
---|---|
University of Chicago |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in home BP | systolic pressure over diastolic pressure; measured by Bluetooth enabled, electronic, at home BP cuff | Baseline, Week 12 | |
Secondary | Change in BP control rate | measured by clinical BP cuff, BP control defined as clinically-measured BP < 140/90 mmHg | Baseline, Week 12 | |
Secondary | Change in medication adherence | measured by Morisky Medication Adherence Scale [Morisky Scale (MMAS-8)]; minimum value is 0, maximum value is 8; lower values indicate worse medication adherence | Baseline, Week 12 | |
Secondary | Number of EPIC myChart patient-provider messages and replies | total number of messages and replies | Week 12 | |
Secondary | Number of hypertension related unscheduled emergency department or urgent care visits | total number of visits | Week 12 |
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