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Completed

NCT Number: NCT05302193

Non-invasive Blood Pressure Measurement Using Samsung Smartwatch

The aim of this study is to verify the accuracy of blood pressure and heart rate measurement by Samsung smartwatches compared to a standard monitor of vital signs used in intensive care units.

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Key information

Age range

15 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Faculty of Biomedical Engineering, Czech Technical University in Prague

Kladno, 27201, Czechia

About this study

Recently, wearables, like smartwatches, have been gaining new possibilities in monitoring biological signals and they are used for home monitoring of health conditions. Heart rate measurement is a common function of smartwatches, some smartwatch models even measure blood pressure. The study aims to compare the measurement of blood pressure and heart rate using the latest smartwatch with a vital signs monitor used in clinical practice. Blood pressure and heart rate measurements will be taken by hand from the watch and the vital signs monitor simultaneously. The agreement of the measurements of both devices will be evaluated.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • healthy volunteers

Exclusion criteria

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

Treatment and study plan

Calm measurement of blood pressure and heart rate (before physical activity)

Other

Simultaneous blood pressure and heart rate measurements at minutes 2 and 5.5 of the experiment.

Physical activity

Other

Five minutes of physical activity, between times 7.5 min and 12.5 min of the experimental part. Riding on a spinning ergometer with a standardized load of 1 W/kg.

Calm measurement of blood pressure and heart rate (after physical activity)

Other

Simultaneous blood pressure and heart rate measurements at times 15.5, 17, 20.5 and 22 minutes of the experimental part.

Primary outcomes

  1. Similarity of blood pressure measurements from two devices

    Time frame: 1 hour

    The agreement of systolic and diastolic blood pressure measurements of both monitoring devices will be evaluated.

  2. Similarity of heart rate measurements from two devices

    Time frame: 1 hour

    The agreement of heart rate measurements of both monitoring devices will be evaluated.

Sponsors and collaborators

Lead sponsor

Czech Technical University in Prague

Other

Registry information

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Mar 31, 2022
Registry last updated
Mar 25, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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