A team-based approach to improve hypertension control

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study compares a multidisciplinary intervention aimed at addressing both clinical and social needs for hypertension management against enhanced standard care in primary care clinics. It focuses on the unique challenges faced by African American and Latinx populations in Chicago, particularly on the West Side, where significant health disparities exist. The intervention includes remote monitoring and education programs tailored to the specific needs of the community, with the goal of improving hypertension control outcomes. By integrating clinical care with community resources, the study aims to reduce the life expectancy gap related to cardiovascular disease in this region.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Adults 18 years or older
* African American and/or Latinx
* Uncontrolled stage 2 hypertension, BP \>/= 140/90
* Patient is following with Rush primary care provider in eligible Rush primary care clinics
* Patient has a smart phone (Android or iOS)
* Patient has an email

Exclusion Criteria:

* Organ transplant recipient
* On dialysis
* Patient is already participating in another remote hypertension monitoring program
* Patient is not interested in participating in the program
* Patient has already participated in the E3 Hypertension program or the E3 Diabetes program

Where it's running

• Rush University Medical Center
  Chicago, Illinois, United States Recruiting

Study contacts

• Principal investigator: Kristen Pallok, MD — Rush University Medical Center
• Study coordinator: Kristen Pallok, MD
• Email: Kristen_N_Pallok@rush.edu
• Phone: 13129426700

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.