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Completed
NCT07740850
Virtual Reality for Procedural Pain During IV Cannulation in Children
Conditions: Procedural Pain
Sex: All
Ages: 6 Years – 11 Years
Healthy volunteers: Yes
Phase: NA
Enrollment: 150
Sponsor: Ege University
Location: Ege University Izmir
Summary
This study evaluates whether virtual reality (VR)-based distraction can reduce pain during intravenous cannulation and venous blood sampling in children treated in a pediatric emergency department. Children aged 6-11 years who required these procedures received either standard care or VR distraction using age-appropriate audiovisual content. The primary outcome was procedure-related pain measured by the Wong-Baker FACES Pain Rating Scale. Secondary outcomes included procedural duration, cooperation, first-attempt success, behavioral distress, and parental satisfaction. The study also explored whether the effectiveness of VR was associated with patient engagement during the procedure.
Eligibility Criteria
Inclusion Criteria:
* Children aged 6-11 years
* Requirement for intravenous cannulation or venous blood sampling in the -pediatric emergency department
* Ability to understand and engage with virtual reality content
* Written informed consent obtained from parent or legal guardian
Exclusion Criteria:
* Visual or hearing impairment preventing VR use
* Neurological or developmental disorders affecting communication or cooperation
* Altered level of consciousness
* Hemodynamic instability requiring immediate intervention
* Previous participation in the study
* Refusal of participation by the child or parent/legal guardian
* Contraindications to virtual reality exposure (e.g., severe motion sickness or intolerance)
Source: ClinicalTrials.gov (NCT07740850). StuddyBuddy aggregates publicly available trial information.