NCT04163809 · Cedars-Sinai Medical Center
The Role of Virtual Reality During Regional Anesthesia
What this study is about
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.
View original scientific description
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.
Interventions
DEVICE
Virtual Reality with Oculus Go headset
The 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.
Primary outcome measures
Anxiety Level Prior to Regional Anesthesia
Time frame: questionnaire given within 1 hour prior to regional anesthesia procedure
questionnaire to rate anxiety on a scale of 0-10
Anxiety Level During Regional Anesthesia
Time frame: questionnaire given within 1 hour after regional anesthesia procedure
questionnaire to rate anxiety on a scale of 0-10
Pain Level Prior to Regional Anesthesia
Time frame: questionnaire given within 1 hour prior to regional anesthesia procedure
questionnaire to rate pain on a scale of 0-10
Pain Level During Regional Anesthesia
Time frame: questionnaire given within 1 hour after regional anesthesia procedure
questionnaire to rate pain on a scale of 0-10
Who can participate
This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.
Inclusion criteria
- 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
Exclusion criteria
- Patients under the age of 18 \& above age 64
- Visual impairment
- Pregnant women
- Diagnosis of epilepsy/seizures, dementia, and/or cognitive impairment
Where
- Los Angeles, California
Related conditions & keywords
Frequently asked questions
What is a clinical trial?
A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.
Is it safe to participate?
Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.
Will I be compensated?
Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.
Will I receive a placebo instead of treatment?
When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.
Can I leave a trial if I change my mind?
Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.
How long does a clinical trial last?
Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.
Data: ClinicalTrials.gov · synced May 14, 2025 · Source of record for eligibility and locations