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Recruiting NCT07322523

Smartwatch Accuracy for Measuring Vitals and Anxiety Before Disc Surgery

Trial Parameters

Condition Disc Herniations
Sponsor Halil Kalaycı
Study Type OBSERVATIONAL
Phase N/A
Enrollment 60
Sex ALL
Min Age 22 Years
Max Age N/A
Start Date 2025-11-01
Completion 2026-03-30

Brief Summary

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.

Eligibility Criteria

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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