Using virtual reality to reduce anxiety and fear in patients before abdominal surgery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial investigates the impact of virtual reality applications on anxiety and fear levels in patients scheduled for abdominal surgery. Participants will use VR glasses to watch nature scene videos in the preoperative area, while their anxiety levels will be assessed through a surgical fear questionnaire. The study employs a randomized, controlled, single-blind design to compare the effects of virtual reality against routine nursing care. The goal is to determine if virtual reality can effectively alleviate preoperative anxiety and fear in this patient population.

Why it matters

Who can join: the full rules

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

Where it's running

• Balcali Hospital Health Application and Research Center
  Adana, Sarıçam, Turkey (Türkiye) Recruiting

Study contacts

• Study coordinator: Nursevim A research assistant
• Email: nursevimaydingulu@gmail.com
• Phone: +905458504330

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.