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Smartwatch Accuracy for Measuring Vitals and Anxiety Before Disc Surgery

Recruitingn/aAges 22 Years - anyAllHalil Kalaycı
NCT07322523 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This study aims to verify the accuracy of blood pressure, heart rate, blood oxygen saturation, anxiety level, and sleep cycle data measurements obtained from Samsung smartwatches compared to the currently accepted method used in patients with disc herniation undergoing the preoperative period.

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📋 Eligibility rules (as published)
Inclusion Criteria: * 22 years and older * Currently receiving preoperative care/assessment for disc herniation surgery. * No history of any cardiovascular disease other than controlled hypertension. * Willingness to wear the smartwatch for a minimum of 8 consecutive hours during the night before surgery. * Ability to follow all instructions related to the smartwatch operation and data collection independently. * No known allergy to nickel. Exclusion Criteria: * Patients who are currently receiving prescribed medication specifically for sleep in the clinical setting. * Refusal or unwillingness to participate in the study. * The participant fails to wear the smartwatch correctly or appropriately as per study instructions, leading to incomplete or unreliable data collection.
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What it tests

  • Not listed
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Where

1 site
Erciyes University
Kayseri, Turkey (Türkiye)
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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