Optimizing Sustainable Cuff Access and Training Pathways for Self-Measured Blood Pressure Monitor… (NCT07693699) | Clinical Trial Compass
RecruitingNot Applicable
Optimizing Sustainable Cuff Access and Training Pathways for Self-Measured Blood Pressure Monitoring in Primary Care
United States150 participantsStarted 2026-07-30
Plain-language summary
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?
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1This trial focuses on training patients and providing cuffs for home blood pressure monitoring — how would my doctor or care team actually walk me through using a home cuff correctly, and what does that training process look like in practice?
2Since the trial is measuring whether patients successfully complete cuff orders and training, what happens if I have trouble accessing or affording a blood pressure cuff — is there support built into this study to help with that?
3This study is in primary care settings and is focused on the process of getting patients set up with self-monitoring rather than testing a new medication — does my doctor think home blood pressure monitoring would give a more accurate picture of my blood pressure than readings taken only in the office?
4Since this is a non-drug study focused on logistics and training, are there any risks or burdens I should be aware of — like extra appointments, data sharing, or requirements that might be hard to fit into my schedule?
5Would my doctor recommend I try self-measured blood pressure monitoring as a standard part of my care right now regardless of this trial, or is joining the study the main way to get structured support and equipment for doing it at home?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.