Technology-enabled Management Versus Usual Care for Blood Pressure
Sponsored by Stanford University
About this study
Two arm parallel randomized clinical trial
For this study, we have 3 cohorts that employ varying recruitment strategies before they are enrolled in the interventions. At Stanford, we have 2 cohorts, where Cohort 1 is recruiting participants through clinic screening and contacting them through text or email. For Cohort 2, recruitment is divided into two phases: Control Phase I and Intervention Phase II. During Control Phase I, standard recruitment methods were employed, including general outreach through participating clinics and pre-existing clinical networks. These efforts did not incorporate specific strategies aimed at enhancing diversity or prioritizing underrepresented populations. In contrast, Intervention Phase II introduced four targeted strategies designed to improve the inclusion of African-American, Hispanic/Latinx ind…
Where this study is enrolling (3)
- I'm interested
Stanford Health Care
Palo Alto, California
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Lake Country Medical Group
Eatonton, Georgia
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Morehouse School of Medicine
Atlanta, Georgia
Who can participate
Inclusion criteria
- ✓Age 30-90 yrs.
- ✓Smartphone ownership
- ✓Office SBP: ≥ 140 mm Hg
- ✓≤ 2 current anti-HTN meds
- ✓Able to add or dose-increase at least 2 of the following classes of medications: ACE-I/ARB, diuretic, calcium channel blocker, beta-blocker, mineralocorticoid receptor antagonists (i.e., at least 2 classes are available for addition or dose- increases after excluding intolerant medications and medications currently at maximum dose)
- ✓English or Spanish-speakers
Exclusion criteria
- ✕Heart failure with reduced ejection fraction (EF \< 40%)
- ✕ESRD (GFR \<15)
- ✕Renal replacement therapy
- ✕Pregnant
- ✕Myocardial infarction or stroke within preceding 6 months
- ✕Hospitalization for hypertensive emergency or malignant hypertension within preceding 6 months
- ✕Prior solid organ transplantation
- ✕At the clinical discretion of the investigators
- ✕Enrolled in another clinical study
Only the research team can confirm whether you qualify. The intake questionnaire is the best way to find out.
Completing a questionnaire on Clinably does not enroll you in a clinical trial or confirm your eligibility. Only the research team can determine whether you qualify to participate. These results are based on the information you provide and are intended to help you start a conversation with the research team.
Trial data sourced from ClinicalTrials.gov.