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Role of Wrist Based Blood Pressure Monitoring in Clinical Practice

S

Scripps Translational Science Institute

Status

Withdrawn

Conditions

Transitions of Care
Blood Pressure

Study type

Observational

Funder types

Other

Identifiers

NCT03862742
IRB-18-7223

Details and patient eligibility

About

This is a pilot clinical study to test the overarching hypothesis that frequent and longitudinal blood pressure monitoring with FDA approved consumer wrist based device during the patient transition from inpatient to home to the first clinic visit will elicit valuable BP data that can assist in physician treatment of hypertension

Full description

Wrist based health devices, often with mobile connectivity, that continuously or near continuously track heart rate, blood pressure, temperature, activity and sleep are growing in everyday popularity and beginning to enter the sphere of clinical relevance. However, their accuracy and utility for clinical use is largely unstudied. As these consumer devices, some of which are FDA approved, become more commonplace, it is paramount to understand their function, know their limitations, and be able to interpret results appropriately before incorporating them into our clinical practice. The AHA/ACC 2017 guideline makes a 1A recommendation for clinical use of out of office BP measurements(1). This recommendation is based on evidence that out of office BP and frequent and longitudinal BP measurements are important in predicting cardiovascular risk and monitoring treatment efficacy(2-5). This trend towards consumer driven digital health monitoring and the new AHA/ACC guideline are essentially advancing a consumer based precision medicine strategy for diagnosis and monitoring of hypertension. As this becomes commonplace in our patient population, we need rigorous clinical study of wrist base BP monitoring to better understand its role patient care.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ≥18 years of age
  • Own an iOS or Android device

Exclusion criteria

  • Inability to give informed consent
  • <18 years of age
  • Inability to understand written English language
  • Hypertensive urgency or emergency as an admission diagnosis

Trial design

0 participants in 1 patient group

Patients admitted to the hospital
Description:
We will recruit patient volunteers from the Scripps Green Hospital and Scripps Memorial Hospital inpatient teaching services.

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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