Accuracy Testing of Validated and Non-validated Home BP Devices Sold on the Online Market.

Last updated: February 12, 2025
Sponsor: Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal
Overall Status: Active - Recruiting

Phase

N/A

Condition

Williams Syndrome

Stress

Circulation Disorders

Treatment

awake ABPM

Clinical Study ID

NCT06688409
VALID-HomeBP
  • Ages > 18
  • All Genders

Study Summary

This study aims to assess whether validated and non-validated blood pressure measuring devices sold on the online market are accurate in regards to the mean awake BP from ambulatory blood pressure monitoring.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Adults aged > 18 years scheduled to undergo an ABPM

Exclusion

Exclusion Criteria:

  • Upper arm size outside of cuff range of selected devices (<22 cm or >42 cm)

  • Night shift workers

  • Permanent atrial fibrillation

  • Known severe aortic stenosis

  • Contraindication to measure BP on the non-dominant arm

  • Ongoing pregnancy

  • Inability or unwillingness to provide consent

Study Design

Total Participants: 140
Treatment Group(s): 1
Primary Treatment: awake ABPM
Phase:
Study Start date:
February 12, 2024
Estimated Completion Date:
November 30, 2027

Connect with a study center

  • Hôpital Sacré-Coeur de Montréal

    Montreal, Quebec H4J 1C5
    Canada

    Active - Recruiting

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