Optimizing Sustainable Cuff Access and Training Pathways for Self-Measured Blood Pressure Monitoring in Primary Care

ConditionHypertension
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorWake Forest University Health Sciences

About this trial

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?

Eligibility criteria

Qualifiers

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.

Disqualifiers

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.

Trial design

Treatments tested in this trial

  • In-Clinic Cuff Delivery - Enhanced Return Conversation
  • In-Clinic Cuff Delivery - Written Instructions
  • Mail Order Cuff Delivery - Enhanced Return Conversation
  • Mail Order Cuff Delivery - Written Instructions

Treatment groups

150 Participants
are divided into 4 treatment groups