Effect of Virtual Reality Before Upper Gastrointestinal Endoscopy on Preprocedural Anxiety, Psychological Readiness, and Postprocedural Satisfaction

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorArdahan University

About this trial

Objective: This study aims to evaluate the effect of virtual reality applied before upper gastrointestinal endoscopy on preprocedural anxiety, psychological readiness, and postprocedural satisfaction.

Methods: This randomized controlled trial will be conducted in the Endoscopy Unit of Kelkit State Hospital. A total of 64 patients scheduled to undergo upper gastrointestinal endoscopy will be enrolled and randomly assigned in a 1:1 ratio to either the virtual reality intervention group or the control group. Participants in the intervention group will receive a virtual reality application before the endoscopy procedure, whereas participants in the control group will receive standard care. Data will be collected using the Endoscopy Patient Information Form, the State Anxiety Inventory (STAI-I), a single-item Psychological Readiness Assessment, and a single-item Postprocedural Satisfaction Assessment. Anxiety and psychological readiness will be evaluated before the procedure, and patient satisfaction will be assessed immediately after the procedure.

Expected Results: It is anticipated that the virtual reality intervention will reduce preprocedural anxiety, improve psychological readiness, and increase postprocedural satisfaction compared with standard care.

Eligibility criteria

Qualifiers

Aged 18 years or older

Scheduled to undergo upper gastrointestinal endoscopy

Able to understand and communicate in Turkish

Willing to participate in the study

Disqualifiers

Presence of a diagnosed psychiatric or neurological disorder that may interfere with participation

Presence of a visual, hearing, head, face, or eye condition that prevents the use of a virtual reality headset

History of severe vertigo, motion sickness, or balance disorder

Development of severe dizziness, nausea, eye strain, or discomfort during the virtual reality intervention

Trial design

Treatments tested in this trial

  • Virtual Reality
  • Standard Preprocedural Care

Treatment groups

52 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Ardahan University

Lead sponsor

Gümüşhane Universıty

Collaborator