The purpose of this study is to determine if non-invasive distracting devices (Virtual Reality headset) are more effective than the standard of care (i.e., no technology based distraction) for preventing anxiety in parental and pediatric populations with limited English proficiency (LEP).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Enrollment
44
Virtual Reality headset with calming scenery
Lucile Packard Children's Hospital Stanford
Palo Alto, California, United States
Procedural-Related Anxiety
Validated questionnaires regarding anxiety will be administers pre- and post-intervention (i.e virtual reality) and compared to those in the control arm (i.e no virtual reality)
Time frame: Duration of intervention, approximately 20-30 minutes
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.