Smartwatch Accuracy for Measuring Vitals and Anxiety Before Disc Surgery

Recruiting now

Conditions studied: Disc Herniations, Disc Herniation, Lumbar, Cervical Disc Herniation, Preoperative Anxiety Score, Sleep Quality, Preoperative Care, Vital Signs Monitoring, Smart Watch, Wearable Devices, Surgical Nursing

In brief

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.

Key facts

Study ID

NCT07322523

Run by

Halil Kalaycı

People needed

60

Starts

2025-11-01

Expected to finish

2026-03-30

Last updated by the study team

2026-01-07

Who can join

Age: 22 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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.

You may not qualify if…

• 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.

Where it is running

• Erciyes University — Kayseri, Turkey (Türkiye) (enrolling)

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.