Ireland
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Recruiting Not applicable

Effect of Virtual Reality Application on Anxiety and Fear in Patients

NCT06830330 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2024-08-20
Last updated
2025-02-25

Condition(s) studied

Preoperative PatientsPatients Undergoing Abdominal Surgery

Investigational drug(s) / intervention(s)

Virtual reality

Virtual reality: Patients in the experimental group were shown videos of natural landscapes with VR glasses in their beds. This application was used to distract patients who were experiencing negative emotions just before surgery. The video session begins with the introduction of the virtual reality glasses. A motionless virtual area is determined at the point where the patient's stretcher is located. The glasses are placed on the patient's head and both hands of the patient are trained to use the remote control. Video content is selected and started according to the patient's preference. Video sessions last approximately 10 minutes.

Study summary

The goal of this clinical trial is to learn if virtual reality application effects on anxiety and fear in patients who will undergo abdominal surgery.

It will also learn about the practical of virtual reality application in preoperative theatre. The main questions it aims to answer are:

* Does virtual reality reduce patient anxiety levels before surgery?
* Is virtual reality useful for patients to watch videos in the preoperative area? Researchers will compare virtual reality videos to routine nursing care to see if virtual reality works to treat preoperative anxiety and surgical fear.

Participants will:

* watch videos of nature scenes with VR glasses in the waiting area before surgery.
* answer the surgical fear quastionairre items for preoperative fear test

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients scheduled for abdominal surgery under general anesthesia using the laparoscopic method * Patients who can communicate * Patients who agree to participate in the study * Patients over the age of 18 Exclusion Criteria: * Patients who use glasses * Patients with an ASA score above 3 * Patients with vertigo and motion sickness * Patients with known psychiatric or behavioral diagnoses

Primary outcome measure(s)

  • State Anxiety Level Change — The state anxiety scale were applied to the patients 15 minutes after they watched the video with virtual reality glasses.
    The effect of virtual reality intervention on preoperative anxiety level is safely evaluated.

Trial sites (1)

FacilityCityRegionStatus
Balcali Hospital Health Application and Research Center Adana Sarıçam Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06830330 on ClinicalTrials.gov ↗ ← All trials in Turkey