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Virtual Reality Adjunct for Procedural Pain and Anxiety Management in Burn Wound Care

Study acronym: VR-Burn
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated April 6, 2025 (before its estimated May 25, 2026 completion). Its status may not reflect the trial's current state.

Record History

  1. Minor Study First Submitted
This randomized controlled trial is designed to evaluate the efficacy of immersive virtual reality (VR) as an adjunct to standard analgesia during dressing changes in adult burn patients. The study compares an intervention group receiving standard care combined with an immersive VR distraction (using a head-mounted display displaying an engaging virtual environment) versus a control group receiving standard care plus non-VR distraction (watching a nature video on a tablet). The primary outcomes include procedural pain intensity measured by the Visual Analog Scale (VAS) and anxiety levels measured by the State-Trait Anxiety Inventory (STAI). Secondary outcomes include patient satisfaction and physiological parameters (heart rate and blood pressure) recorded during the procedure. This trial addresses the critical gap of heterogeneity and small sample sizes noted in previous VR studies for burn care pain management (Dascal et al., 2017).
Trial Details
NCT Number NCT06913270
Lead Sponsor Al Hayah University In Cairo
Conditions
(from sponsor)
Burns, Burn Wound, Procedural Pain, Anxiety Acute
Related terms Burns, Procedural Pain
Enrollment 100 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov