Optimizing Sustainable Cuff Access and Training Pathways for Self-Measured Blood Pressure Monitoring in Primary Care
Optimizing Sustainable Cuff Access and Training Pathways for Self-Measured Blood Pressure Monitoring in Primary Care: A Pragmatic Randomized Controlled Trial
Who can join
As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.
- Age
- 18 Years and older
- Sex
- All sexes
- Healthy volunteers
- Not accepted
- Compensation
- Not stated
Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.
What to expect
No one can promise a trial will help you personally — that is what the research is trying to find out.
What participation involves
Not stated in the study description — ask the study team about visits and procedures.
- Compensation
- Not stated
- Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
- Participants are monitored closely by the research team throughout the study.
- Some participants may receive access to an investigational treatment, which is still being studied.
- Your participation helps researchers learn whether this approach could help future patients.
About this study
The goal of this study is to identify what cuff delivery and BP log return modality most effectively achieve successful delivery of a self-measured blood pressure (SMBP) intervention in routine care, among adult primary care patients with uncontrolled hypertension?
Compensation is read from the study's own description and may be missing — always confirm with the study team.
Eligibility
Official eligibility criteria
Inclusion Criteria: * Age 18 years or older. * Diagnosed hypertension documented prior to the index clinic visit. * Scheduled for and attends an in-person visit with a participating clinician at a study clinic. * Elevated BP (blood pressure) documented in Epic during rooming or the clinic visit before study enrollment, defined as systolic BP \>=140 mmHg or diastolic BP \>=90 mmHg. Exclusion Criteria: * Visit is canceled, rescheduled, or the patient does not attend the visit. * Patient already has a usable home BP cuff provide through insurance within the past 5 years. * Patient declines assistance obtaining a BP cuff. * Patient declines submitting cuff order to insurance. * Patient unable to participate for operational reasons.
Study sites (6)
IL
- Advocate Medical Group Chicago (Southeast) · Chicago, IL 60617Nicole Glowacki, MPH · Study contact · 708-684-3691 · nicole.glowacki@aah.orgMore trials in Chicago
- Advocate Medical Group Chicago (Imani Village) · Chicago, IL 60619Nicole Glowacki, MPH · Study contact · 708-684-3691 · nicole.glowacki@aah.orgMore trials in Chicago
- Advocate Medical Group Beverly · Chicago, IL 60643Nicole Glowacki, MPH · Study contact · 708-684-3691 · nicole.glowacki@aah.orgMore trials in Chicago
- Advocate Medical Group Merrionette Park · Merrionette Park, IL 60803Nicole Glowacki, MPH · Study contact · 708-684-3691 · nicole.glowacki@aah.orgMore trials in Merrionette Park
- Advocate Medical Group Oak Lawn (FP) · Oak Lawn, IL 60453Nicole Glowacki, MPH · Study contact · 708-684-3691 · nicole.gowacki@aah.orgMore trials in Oak Lawn
- Advocate Medical Group Oak Lawn (IM) · Oak Lawn, IL 60453Nicole Glowacki, MPH · Study contact · 708-684-3691 · nicole.glowacki@aah.orgMore trials in Oak Lawn