Actively Recruiting

Phase Not Applicable
Age: 18Years - 99Years
All Genders
NCT06391073

Reach Out 2: Emergency Department-Initiated Hypertension Mobile Health Intervention Connecting Multiple Health Systems

Led by Northwestern University · Updated on 2025-07-24

500

Participants Needed

1

Research Sites

227 weeks

Total Duration

On this page

Sponsors

N

Northwestern University

Lead Sponsor

U

University of Michigan

Collaborating Sponsor

AI-Summary

What this Trial Is About

Emergency department visits provide an opportunity to identify people with undiagnosed, untreated, or uncontrolled high blood pressure. In Reach Out, we will test whether a mobile health intervention yields a greater reduction in blood pressure than usual care among individuals identified with high blood pressure during a safety-net emergency department visit. Subsequently, we will estimate the reduction in heart attack, stroke, and dementia if Reach Out were implemented across all U.S. safety-net emergency departments.

CONDITIONS

Official Title

Reach Out 2: Emergency Department-Initiated Hypertension Mobile Health Intervention Connecting Multiple Health Systems

Who Can Participate

Age: 18Years - 99Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older
  • At least one blood pressure reading with systolic BP of 160 or higher or diastolic BP of 100 or higher while in the emergency department
  • If repeat blood pressure measurements are taken after initial high reading, at least one repeat reading has systolic BP of 140 or higher or diastolic BP of 90 or higher
  • Must have a cell phone capable of receiving text messages
  • Likely to be discharged from the emergency department
Not Eligible

You will not qualify if you...

  • Critically ill patients
  • Unable to read English
  • Currently incarcerated
  • Pregnant at the time of the study
  • Pre-existing condition that makes 6-month follow-up unlikely

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Hurley Medical Center

Flint, Michigan, United States, 48503

Actively Recruiting

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Research Team

L

Lesli Skolarus, MD, MS

CONTACT

W

William Meurer, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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