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Clinical Trials/NCT05401435
NCT05401435UnknownNot Applicable

Reliability of Measuring Blood Pressure With a Smartwatch

Czech Technical University in Prague1 site in 1 country15 target enrollmentStarted: May 4, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
15
Locations
1
Primary Endpoint
Change in long-term similarity of heart rate measurements from two devices

Study Overview

Brief Summary

The aim of this study is to verify the long-term accuracy of blood pressure and heart rate measurements by Samsung smartwatches between two consecutive calibrations compared to a standard digital tonometer used in clinical practice and for home measurement of these vital parameters.

Detailed Description

Recently, smartwatches can measure a wide range of biological signals, including heart rate and blood pressure. The short-term reliability of blood pressure measurements after the required calibration has been studied, but long-term reliability is still a question. The aim of the project is to experimentally evaluate the reliability of long-term blood pressure measurement with a Samsung smart watch between two consecutive calibrations over a period of 28 days in comparison with a digital tonometer (Omron) approved as a medical device. Volunteers will measure blood pressure and heart rate manually twice a day from a smartwatch and a digital tonometer simultaneously. The agreement of the measurements of both devices will be evaluated.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •healthy volunteers

Exclusion Criteria

  • •any acute illness
  • •pregnancy
  • •severe cardiovascular conditions
  • •severe asthma or other severe respiratory conditions
  • •hypotension or hypertension

Arms & Interventions

Blood pressure and heart rate measurement

Experimental

Resting blood pressure and heart rate measurement regularly one value in the morning and evening for 28 days. The volunteer measures the parameters simultaneously on both devices (smartwatch and digital tonometer). In total, each participant will undergo this measurement 56 times.

Intervention: Resting measurement of blood pressure and heart rate (Other)

Outcomes

Primary Outcomes

Change in long-term similarity of heart rate measurements from two devices

Time Frame: 28 days

The long-term agreement of heart rate measurements of both monitoring devices will be evaluated. This means that we evaluate the changes in the similarity of measured heart rates over a period of 28 days.

Change in long-term similarity of blood pressure measurements from two devices between two consecutive calibrations

Time Frame: 28 days

The long-term agreement of systolic and diastolic blood pressure measurements of both monitoring devices between two consecutive smartwatch calibrations will be evaluated. This means that we evaluate the changes in the similarity of measured blood pressures over a period of 28 days.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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