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Behavioural Intervention

Virtual Reality analgesia for Anxiety

N/A
Waitlist Available
Led By Michelle Stern, MD
Research Sponsored by New York City Health and Hospitals Corporation
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year
Awards & highlights

Study Summary

Virtual Reality Analgesia In Trauma Rehab

Eligible Conditions
  • Virtual Reality Analgesia
  • Anxiety
  • Musculoskeletal Pain
  • Virtual Reality
  • Opioid Use Disorder
  • Traumatic Injury

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year
This trial's timeline: 3 weeks for screening, Varies for treatment, and 1 year for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Pain
Secondary outcome measures
Blood Pressure
Heart Rate
Increase or decrease in opioid/oral pain medication use
+1 more

Trial Design

2Treatment groups
Active Control
Group I: ControlActive Control1 Intervention
Trauma patients in rehab unit in the participating hospital will be included in this arm if they are randomized to receive no intervention
Group II: Virtual Reality analgesiaActive Control1 Intervention
Trauma patients in rehab unit in the participating hospital will be included in this arm if they are randomized to receive the intervention which is a virtual reality headset providing immersive interactive content in the video format

Find a Location

Who is running the clinical trial?

New York City Health and Hospitals CorporationLead Sponsor
32 Previous Clinical Trials
8,419 Total Patients Enrolled
Michelle Stern, MDPrincipal InvestigatorNew York City Health and Hospitals Corporation

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