Clinical Trial

Comparison of Virtual Reality-Based and Routine Preoperative Education on Surgical Anxiety and Salivary Cortisol

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Record status
This record was last updated March 2, 2026 (before its estimated April 27, 2026 completion). Its status may not reflect the trial's current state.
Summary
This randomized controlled pilot study aims to compare the effects of virtual reality-based preoperative education and routine preoperative education on surgical anxiety in patients undergoing lumbar disc surgery. In addition to evaluating psychological outcomes, the study will also compare psychometric anxiety assessments with a biological stress marker, salivary cortisol, to examine the relationship between subjective and physiological stress responses. Preoperative anxiety is common among surgical patients and may negatively influence both emotional well-being and physiological stress regulation. Virtual reality-based education may provide a more immersive and engaging learning experience compared to routine education, potentially reducing anxiety levels. Participants will be randomly assigned to either a virtual reality-based education group or a routine preoperative education group. Surgical anxiety will be assessed using validated psychometric measurement tools, and physiological stress response will be evaluated through salivary cortisol analysis. The study will further explore the concordance between psychometric findings and biological stress indicators. The results may contribute to the development of innovative, evidence-based nursing interventions and provide insight into the relationship between psychological and biological indicators of preoperative anxiety.
Trial Details
NCT Number NCT07443111
Lead Sponsor Bezmialem Vakif University
Conditions Lumbar Disc Herniation, Preoperative Anxiety
Enrollment 56 participants
Start Date 2026-02-27
Primary Completion 2026-04-27 (estimated)
Study Completion 2026-05-27 (estimated)
Updated on ClinicalTrials.gov 2026-03-02