Smartwatch Accuracy for Measuring Vitals and Anxiety Before Disc Surgery
Recruiting · NCT07322523 · Observational (researchers observe without assigning treatment) · Lead sponsor: Halil Kalaycı
View the official record on ClinicalTrials.gov →What this trial is about
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.
Who can take part
Age range
22 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
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 surgery.
- Ability to follow all instructions related to the smartwatch operation and data collection independently.
- No known allergy to nickel.
Exclusion criteria
- 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
1 location listed.
- Erciyes University - Kayseri, Turkey (Türkiye)