Trials / Recruiting
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
- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 60 (estimated)
- Sponsor
- Halil Kalaycı · Academic / Other
- Sex
- All
- Age
- 22 Years
- Healthy volunteers
- Not accepted
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.
Conditions
- Disc Herniations
- Disc Herniation, Lumbar
- Cervical Disc Herniation
- Preoperative Anxiety Score
- Sleep Quality
- Preoperative Care
- Vital Signs Monitoring
- Smart Watch
- Wearable Devices
- Surgical Nursing
Timeline
- Start date
- 2025-11-01
- Primary completion
- 2026-03-30
- Completion
- 2026-03-30
- First posted
- 2026-01-07
- Last updated
- 2026-01-07
Locations
1 site across 1 country: Turkey (Türkiye)
Source: ClinicalTrials.gov record NCT07322523. Inclusion in this directory is not an endorsement.