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24-Hour Ambulatory Blood Pressure Monitoring in Community Pharmacies

Not Applicable
Completed
Conditions
Hypertension
Interventions
Other: ABPM service by Pharmacists
Registration Number
NCT03920956
Lead Sponsor
Virginia Commonwealth University
Brief Summary

This study is designed to explore the feasibility of providing 24-hour ambulatory blood pressure monitoring in community pharmacies. The investigators hypothesize it will be feasible for community pharmacies to provide the service to assist medical providers in the diagnosing and management of high blood pressure. The investigators will also survey participants regarding their experience with the service as well as conduct interviews with participating pharmacists and medical providers to understand their views and opinions on the feasibility of the service.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
53
Inclusion Criteria
  • Adults greater than or equal to 18 years of age suspected by their physician of having "white coat" or "masked" hypertension (HTN), hypotension symptoms due to antihypertensive therapy, uncontrolled sustained HTN, requiring additional confirmation of an initial diagnosis if HTN, or resistant HTN.
Exclusion Criteria
  • Documented past medical history of persistent atrial fibrillation, on hemodialysis, pregnancy, or dementia.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Experimental: 24-hour ABPM by PharmacistsABPM service by PharmacistsPatients will meet with the pharmacist to be equipped with a 24-hour ambulatory blood pressure monitor (ABPM). Patients will return the monitor for the pharmacists to download the results to send to their medical provider.
Primary Outcome Measures
NameTimeMethod
Patient satisfaction with the pharmacy service and experience wearing the ABPMup to 72 hours

Patient satisfaction will be assessed using a 9 item survey. Participants will rate items on a 5-point scale from strongly agree to strongly disagree.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Virginia Commonwealth University

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Richmond, Virginia, United States

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