Mobile health intervention for managing high blood pressure in emergency departments
Official title: Reach Out 2: Randomized Clinical Trial of Emergency Department-Initiated Hypertension Mobile Health Intervention Connecting Multiple Health Systems
Run by Northwestern University · NCT06391073 · Data updated 2026-11-12
This study is testing a mobile health program to see if it can help people with high blood pressure who visit the emergency room manage their condition better than regular care.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 99 Years |
| Sex | All |
| Enrollment | 500 (estimated) |
| Sponsor | Northwestern University Academic / other |
| Locations | 1 site (Flint, Michigan) |
| Status | Recruiting |
| Started | July 22, 2024 |
| Main results expected | March 1, 2028 |
| Study ends | November 30, 2028 |
| Registry record updated | July 13, 2026 |
| Trial ID | NCT06391073 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adults aged 18 and older who present with high blood pressure during an emergency department visit.
✕Probably not a fit
Patients who are critically ill, pregnant, or have conditions that would make follow-up unlikely will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to evaluate the effectiveness of a mobile health intervention designed to reduce blood pressure among individuals identified with hypertension during emergency department visits. By leveraging safety-net healthcare systems, the intervention will connect patients with necessary resources, including self-measured blood pressure monitoring and assistance with scheduling physician appointments. The study will compare the outcomes of this intervention against usual care to determine its impact on blood pressure reduction and potential long-term health benefits. The ultimate goal is to address health disparities in hypertension management, particularly among underserved populations.
Why it matters
Potential benefit: If successful, this intervention could significantly lower blood pressure and reduce the risk of heart attacks, strokes, and dementia in underserved populations.
How similar studies have gone: Previous studies, including Reach Out 1, have shown promising results in reducing blood pressure among similar populations, indicating potential for success in this follow-up intervention.
Who can join: the full rules
Show full inclusion / exclusion criteria
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 Exclusion Criteria for Main Trial Participants: * Critical illness * Unable to read English (\<1% at study site) * Incarcerated * Pregnant * Pre-existing condition making 6-month follow-up unlikely
Where it's running
-
Hurley Medical Center
Flint, Michigan, United States Recruiting
Study contacts
- Study coordinator: Lesli Skolarus, MD, MS
- Email: lesli.skolarus@northwestern.edu
- Phone: 312-503-0644
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.