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Clinical Trials/NCT06627920
NCT06627920
Completed
Not Applicable

Validation of a Smartwatch for Blood Pressure Measurement

European University Miguel de Cervantes1 site in 1 country101 target enrollmentJuly 10, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Blood Pressure
Sponsor
European University Miguel de Cervantes
Enrollment
101
Locations
1
Primary Endpoint
Diastolic and systolic blood pressure
Status
Completed
Last Updated
last year

Overview

Brief Summary

Accurate measurement of blood pressure is essential for the assessment of cardiovascular health and the prevention of cardiovascular disease. Smartwatches have emerged as a promising option for continuous monitoring of blood pressure outside the clinical setting. This study aims to validate the use of the smartwatch KC08 for blood pressure measurement, which is a cost-effective and convenient alternative for blood pressure measurement. A cross-sectional study will be conducted with participants aged greater than or equal to18 years. The measurements of blood pressure, heart rate and oxygen saturation will be performed with the smartwatch KC08, the Beurer PO30 pulse oximeter and the Omron M7 BP monitor. The statistical analysis will evaluate the reliability of the devices and compare the measurements of the two devices using different statistical methods.

Registry
clinicaltrials.gov
Start Date
July 10, 2024
End Date
November 21, 2024
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
European University Miguel de Cervantes
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Be ≥18 years old and able to understand the informed consent.

Exclusion Criteria

  • A difference of ≥20 mmHg in systolic and/or diastolic blood pressure between both arms.

Outcomes

Primary Outcomes

Diastolic and systolic blood pressure

Time Frame: 5 minutes rest; 5 minutes safety BP measurements of both arms; 30 minutes BP measurements (10 measurements in total)

For BP measurement, an Omron M7 automatic blood pressure monitor (Omron Healthcare Co., Ltd., Kyoto, Japan) and a KC08 smartwatch (Mediatek Inc., Hsinchu, Taiwan) will be used. The participant should sit in a comfortable chair with lumbar support for at least 5 minutes prior to the measurement. The participant will be asked to place both feet flat on the floor, without crossing the legs, and rest the arm with the cuff on a table at chest level, palm up. Ensuring that the cuff is properly adjusted but not too tight and in contact with bare skin, the blood pressure will be measured. During this process, the subject should refrain from talking to ensure an accurate and reliable reading. The values obtained will be recorded according to standard blood pressure measurement procedures. 10 measurements separated by 1 minute will be taken with each device. The BP results will be recorded in mmHg.

Peripheral oxygen saturation

Time Frame: 30 minutes (10 measurements in total)

A Beurer PO30 pulse oximeter (Beurer GmbH, Mittelstand, Germany) and a KC08 smartwatch (Mediatek Inc., Hsinchu, Taiwan) will be used. 10 measurements separated by 1 minute will be taken with each device. The peripheral oxygen saturation results will be recorded in percentage of hemoglobin saturation.

Physical activity levels

Time Frame: 2 minutes

Participants' physical activity levels will be assessed using the International Physical Activity Questionnaire (IPAQ). This questionnaire consists of 7 questions that will help us stratify physical activity levels. It is used as a descriptive measure of the users and a possible confounding factor. It takes approximately 2 minutes to complete the questionnaire and we do it in the initial interview, before starting with the measurements of BP, heart rate and peripheral oxygen saturation.

Heart rate

Time Frame: 30 minutes (10 measurements in total)

An Omron M7 automatic blood pressure monitor (Omron Healthcare Co., Ltd., Kyoto, Japan), a Beuer PO30 pulse oximeter and a KC08 smartwatch (Mediatek Inc., Hsinchu, Taiwan) will be used. Heart rate will be recorded while blood pressure measurements are being recorded. 10 measurements separated by 1 minute will be taken with each device. The heart rate results will be recorded in beats per minute (bpm).

Study Sites (1)

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