RecruitingNot ApplicableNCT07360678

Comparing the Garmin Venu 3 / Garmin Venu 4 for Non-Invasive Vital Sign Monitoring to a Hospital-Grade Monitor

Sponsor

Ziekenhuis Oost-Limburg

Enrollment

30 participants

Start Date

Oct 12, 2025

Study Type

INTERVENTIONAL

Conditions

Validation of Vital Signs Measured by a Consumer-grade Smartwatch

Summary

This clinical trial evaluates the accuracy of the Garmin Venu 3 / Garmin Venu 4 smartwatch in measuring vital signs (heart rate, respiratory rate, SpO₂) compared to the clinically validated Philips IntelliVue X2. The study aims to determine whether the consumer-grade smartwatch can provide reliable data for remote patient monitoring, early hospital discharge, and chronic disease management, offering a more accessible and affordable alternative to MDR-certified devices.

Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called Garmin Venu 3 or Garmin Venu 4 + Philips Intellivue X2 and Smartwatch rating scale questionnaire for people with validation of vital signs measured by a consumer-grade smartwatch. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEGarmin Venu 3 or Garmin Venu 4 + Philips Intellivue X2

Each participant will be continuously monitored for a minimum of one full night and up to a maximum of 24 hours using both a hospital-grade monitor (Philips IntelliVue X2) and a Garmin Venu 3 or Garmin Venu 4 smartwatch.

OTHERSmartwatch rating scale questionnaire

Upon completion of the monitoring period, participants will be asked to complete the Smartwatch Rating Scale (SRS) questionnaire

Locations(1)

Ziekenhuis Oost-Limburg

Genk, Belgium

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NCT07360678