NCT07322523 Smartwatch Accuracy for Measuring Vitals and Anxiety Before Disc Surgery
| NCT ID | NCT07322523 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Halil Kalaycı |
| Condition | Disc Herniations |
| Study Type | OBSERVATIONAL |
| Enrollment | 60 participants |
| Start Date | 2025-11-01 |
| Primary Completion | 2026-03-30 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 60 participants in total. It began in 2025-11-01 with a primary completion date of 2026-03-30.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief 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.
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 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.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07322523 clinical trial?
This trial is open to participants of all sexes, aged 22 Years or older, studying Disc Herniations. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07322523 currently recruiting?
Yes, NCT07322523 is actively recruiting participants. Contact the research team at halil.kalayci@erciyes.edu.tr for enrollment information.
Where is the NCT07322523 trial being conducted?
This trial is being conducted at Kayseri, Turkey (Türkiye).
Who is sponsoring the NCT07322523 clinical trial?
NCT07322523 is sponsored by Halil Kalaycı. The trial plans to enroll 60 participants.