Using Virtual Reality to Boost Self-Efficacy in Pediatric Patients
Improving Self-Efficacy of Hospitalized Children With Virtual Reality Education: A Pragmatic, Crossover Trial
This study is testing if using Virtual Reality can help kids and young adults feel more confident about their health while they are in the hospital.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 200 (estimated) |
| Ages | 5 Years to 25 Years |
| Sex | All |
| Sponsor | Stanford University Academic / other |
| Locations | 1 site (Palo Alto, California) |
| Trial ID | NCT05725395 on ClinicalTrials.gov |
What this trial studies
This study explores the effectiveness of Virtual Reality (VR) as an intervention to enhance self-efficacy among pediatric patients in a healthcare setting. It aims to compare the impact of an educational VR experience against standard care on self-reported measures of self-efficacy in children and adolescents aged 5 to 25. Participants will alternate between receiving the VR intervention and standard care on different days during their hospital stay, allowing for a direct comparison of outcomes. The study also seeks to establish a profile of short-term psychological well-being in these patients following hospital admission.
Who should consider this trial
Good fit: Ideal candidates are pediatric patients aged 5 to 25 who are admitted to Lucile Packard Children's Hospital.
Not a fit: Patients with a history of seizure disorders, motion sickness, or those who are clinically unstable may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly improve the psychological well-being and self-efficacy of pediatric patients during hospital stays.
How similar studies have performed: While VR has been explored for pain distraction and anxiety reduction, this specific approach to enhancing self-efficacy in pediatric patients is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients' age range from 5 to 25 at LPCH/SHC facilities Exclusion Criteria: * Participants who do not consent * Have a history of seizure disorder * Currently have nausea * Have motion sickness * Are clinically unstable * Currently using corrective glasses (not compatible with VR headset) * Currently pregnant
Where this trial is running
Palo Alto, California
- Lucile Packard Children's Hospital Stanford — Palo Alto, California, United States (Recruiting)
Study contacts
- Study coordinator: Thomas J Caruso, MD, MEd
- Email: tjcaruso@stanford.edu
- Phone: 650-723-5728
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.