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Smartwatch Accuracy for Measuring Vitals and Anxiety Before Disc Surgery

NCT07322523 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 60

Last updated 2026-01-07

No results posted yet for this study

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

Sponsors & Collaborators

  • TC Erciyes University

    collaborator OTHER

  • Halil Kalaycı

    lead OTHER

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-11-01
Primary Completion
2026-03-30
Completion
2026-03-30

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07322523 on ClinicalTrials.gov