← Back to Search

Virtual Reality for Conscious Sedation

N/A
Waitlist Available
Led By Ran Goldman, MD
Research Sponsored by University of British Columbia
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up intraoperative
Awards & highlights

Study Summary

Children often need procedural sedation in the emergency department during painful procedures (such as reducing fractures). Virtual Reality (VR) is an immersive experience using sight, sound, and position sense. Using VR may enhance distraction during the painful procedure and may reduce attention to pain. VR may also reduce anxiety during sedation induction by reducing providing an alternative stimulus. This study will randomize children (6 - 16 years old) to receive Virtual Reality or standard of care while undergoing procedural sedation. Investigators will measure heart rate, blood pressure, satisfaction (child, parent, provider), amount of sedatives used and compare between the two groups.

Eligible Conditions
  • Conscious Sedation

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~immediately after the procedure and by phone the next day
This trial's timeline: 3 weeks for screening, Varies for treatment, and immediately after the procedure and by phone the next day for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change in Blood Pressure as measured by blood pressure monitor
Change in Heart Rate as measured by heart rate monitor
Secondary outcome measures
Emergence Phenomenon as measured by yes/no questions regarding participant experience.
Length of stay in the Emergency Department
Satisfaction among Children by global rating scale
+4 more

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Virtual RealityExperimental Treatment1 Intervention
Participants are distracted by wearing the virtual reality headset and watching a roller coaster app while undergoing procedural sedation
Group II: Standard-of-CareActive Control1 Intervention
Participants are distracted with Standard-of-Care by doctors, nurses, nurse practitioners, child life specialists and/or parents.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Virtual Reality
2017
Completed Phase 3
~1630

Find a Location

Who is running the clinical trial?

University of British ColumbiaLead Sponsor
1,410 Previous Clinical Trials
1,766,507 Total Patients Enrolled
Ran Goldman, MDPrincipal InvestigatorUniversity of British Columbia
2 Previous Clinical Trials
164 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~10 spots leftby Apr 2025