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.
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.
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.