Overview
Purpose: To evaluate the effectiveness and safety of virtual reality (VR) technology in alleviating pain during colonoscopy.
Design and Methods: In the context of a single-centered, prospective, randomized controlled study, the pain levels experienced during colonoscopy are compared between the VR group and the control group.
Description
Patient allocation to either the VR group or the control group will be determined through a randomization process employing sealed opaque envelopes. Patients in the VR group will engage in interactive gaming experiences facilitated by VR devices. The primary outcome measure will be the assessment of pain levels during colonoscopy, which will be quantified using the "Visual Analogue Scale." Additionally, researchers will assess anxiety levels using the "State-Trait Anxiety Inventory" both before and after the colonoscopy procedure. Vital signs during colonoscopy, procedural effects, and adverse effects would also be analyzed.
Eligibility
Inclusion Criteria:
- Between 18 and 50 years of age
- Able to cooperate and complete the questionnaires independently
- Stable vital signs with no serious cardiovascular or cerebrovascular diseases
- Voluntary participation
Exclusion Criteria:
- Severely impaired in vision or hearing to accommodate VR devices
- Previous history of anxiety, depression, cognitive impairment, balance disorder, mental illness, or epilepsy