Reach Out 2: Randomized Clinical Trial of Emergency Department-Initiated Hypertension Mobile Health Intervention Connecting Multiple Health Systems

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 99
Healthy Volunteers: f
View:

⁃ While in the ED, the patient must meet all of the following:

• Adult (≥18 y/o)

• At least one BP with Systolic BP ≥160 or a Diastolic BP ≥100 (criteria 1)

• If the patient has repeated measurements after achieving Criteria 1, at least one of the repeat BP remains systolic BP ≥140 or a diastolic BP ≥90

• Must have cell phones with text-messaging capability

• Likely to be discharged from the ED

Locations
United States
Michigan
Hurley Medical Center
RECRUITING
Flint
Contact Information
Primary
Lesli Skolarus, MD, MS
lesli.skolarus@northwestern.edu
312-503-0644
Backup
William Meurer, MD
Time Frame
Start Date: 2024-07-22
Estimated Completion Date: 2028-11-30
Participants
Target number of participants: 500
Treatments
No_intervention: Usual Care Group
The usual care group is standard of care. They will receive the standard ED discharge materials available as recommended by their ED physician. These materials recommend lifestyle changes, dietary changes, medication as directed, and follow-up with a PCP as directed.
Experimental: REACH OUT
REACH OUT messaging is based on BP control. Control is defined as SMBP \<135/85. Every 4 weeks SMBP measurements will be assessed and mHealth components will be escalated, de-escalated, or remain the same.~If BP is controlled, SMBP prompts will be sent once a week and there will be no facilitated appointments.~If BP is uncontrolled, SMBP prompts will be sent three times per week and facilitated provider scheduling and transportation will occur.~Participants will have the option include a partner, friend, or family member with text-messaging capability who could support them on their BP journey. The partner will receive Reach Out materials and text messages to remind the participant to engage in SMBP and of their upcoming appointments (if uncontrolled).
Sponsors
Collaborators: University of Michigan, Ohio State University
Leads: Northwestern University

This content was sourced from clinicaltrials.gov