EligibleTrials

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

Recruiting · NCT07693699 · Interventional (participants receive a specific treatment) · Lead sponsor: Wake Forest University Health Sciences

View the official record on ClinicalTrials.gov →
Hypertension

Interventions studied

In-Clinic Cuff Delivery - Enhanced Return ConversationIn-Clinic Cuff Delivery - Written InstructionsMail Order Cuff Delivery - Enhanced Return ConversationMail Order Cuff Delivery - Written Instructions

What this trial is about

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 take part

Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)

Inclusion criteria

Exclusion criteria

Where it is running

6 locations listed across 1 US state.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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