Smartwatch Accuracy for Measuring Vitals and Anxiety Before Disc Surgery
Recruiting
Observational Study
Disc Herniations
Disc Herniation, Lumbar
Cervical Disc Herniation
Preoperative Anxiety Score
Sleep Quality
Preoperative Care
Vital Signs Monitoring
Smart Watch
Wearable Devices
Surgical Nursing
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 22 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 60 (estimated)
- Sponsor
- Halil Kalaycı · Other
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About This Trial
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.
Trial Locations
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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 s…
Contacts