RecruitingNCT07322523
Smartwatch Accuracy for Measuring Vitals and Anxiety Before Disc Surgery
Validation of Smartwatch Technology for Preoperative Monitoring of Sleep Quality, Anxiety, and Vital Signs in Patients Undergoing Disc Herniation Surgery
Sponsor
Halil Kalaycı
Enrollment
60 participants
Start Date
Nov 1, 2025
Study Type
OBSERVATIONAL
Conditions
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
Min Age: 22 Years
Inclusion Criteria6
- 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 Criteria3
- 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.
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT07322523
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