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Clinical Trials/NCT05186831
NCT05186831
Completed
Not Applicable

Patient-Portal vs Text-based Hypertension Monitoring Among Black Medicaid/Medicare Patients

University of Pennsylvania1 site in 1 country20 target enrollmentOctober 19, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hypertension
Sponsor
University of Pennsylvania
Enrollment
20
Locations
1
Primary Endpoint
Number of BP measurements reported
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The coronavirus disease 2019 (COVID-19) pandemic has uprooted conventional health care delivery for routine ambulatory care, requiring health systems to rapidly adopt telemedicine capabilities. The digital divide, has been well documented with lower rates of technology and broadband adoption among racial/ethnic minorities. Additionally, Black patients suffer a disproportionate burden of hypertension and cardiovascular disease. This study will implement a text-based home hypertension monitoring program among Black Medicaid patients with hypertension and cardiovascular disease (CVD) and compare its uptake to the currently available blood pressure monitoring program using the patient portal that is integrated into the electronic health record (EHR).

Registry
clinicaltrials.gov
Start Date
October 19, 2020
End Date
January 14, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jennifer Lewey, MD, MPH

Assistant Professor of Medicine

University of Pennsylvania

Eligibility Criteria

Inclusion Criteria

  • Self-identified Black race
  • Medicaid or Medicare insurance
  • Hypertension
  • Cardiovascular disease or presence of at least 1 cardiovascular risk factor
  • Seen for in-person consultation at the Heart and Vascular clinic at the Hospital of the University of Pennsylvania

Exclusion Criteria

  • Does not speak English
  • Already owns a BP cuff
  • Does not have internet access or a phone 15 with texting capabilities

Outcomes

Primary Outcomes

Number of BP measurements reported

Time Frame: 14 days

Number of BP results reported over the study period

Proportion of patients submitting 1 or more BP measurement

Time Frame: 14 days

Proportion of patients per study arm reporting at least one BP measurement

Secondary Outcomes

  • Patient satisfaction(Within 2 weeks of end of study period)

Study Sites (1)

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