About this trial
In this study, we will analyze the role of virtual reality in acute pain and anxiety management for regional anesthesia in pre-operative patients at Cedars-Sinai Medical Center.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Elective pre-operative patients at Cedars-Sinai Medical Center who are receiving regional anesthesia
Between ages 18-64
Patient must be able to provide informed consent
Disqualifiers
Patients under the age of 18 & above age 64
Visual impairment
Pregnant women
Diagnosis of epilepsy/seizures, dementia, and/or cognitive impairment
Trial design
Parallel
Treatments tested in this trial
Virtual Reality with Oculus Go headset
DeviceThe investigator will place the Oculus Go VR headset on the patient. VR will provide distracting, pleasant visual stimulus from the beginning of the procedure (while the patient is being cleaned and draped) and removed immediately after the regional anesthesia procedure is complete for roughly 10-20 minutes. All patients receiving VR will view the same scene.
Treatment groups
Trial outcomes
Primary outcomes
Anxiety Level Prior to Regional Anesthesia
questionnaire to rate anxiety on a scale of 0-10
Anxiety Level During Regional Anesthesia
questionnaire to rate anxiety on a scale of 0-10
Pain Level Prior to Regional Anesthesia
questionnaire to rate pain on a scale of 0-10
Pain Level During Regional Anesthesia
questionnaire to rate pain on a scale of 0-10
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: