RecruitingNot ApplicableNCT06688409
Accuracy Testing of Validated and Non-validated Home BP Devices Sold on the Online Market.
Comparing Home Blood Pressure Measurements from Devices with and Without Evidence of Validation to Ambulatory Blood Pressure Monitoring: the VALID-HomeBP Study
Sponsor
Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal
Enrollment
140 participants
Start Date
Feb 12, 2024
Study Type
INTERVENTIONAL
Conditions
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
Min Age: 18 Years
Inclusion Criteria1
- Adults aged \> 18 years scheduled to undergo an ABPM
Exclusion Criteria7
- 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
Interventions
DIAGNOSTIC_TESTawake ABPM
Comparison of a BP measured with the home BP devices and the average awake ABPM performed immediately after
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06688409
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