The Role of Virtual Reality During Regional Anesthesia

ConditionsAnxietyPain
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-64
SponsorCedars-Sinai Medical Center

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 volunteers

Qualifiers

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

Design model

Parallel

Treatments tested in this trial

  • Virtual Reality with Oculus Go headset

    Device

    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.

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: Control Group (no VR)No intervention 0 interventions
Group B: Experimental Group (VR)Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Anxiety Level Prior to Regional Anesthesia

questionnaire to rate anxiety on a scale of 0-10

Time frame
questionnaire given within 1 hour prior to regional anesthesia procedure
2

Anxiety Level During Regional Anesthesia

questionnaire to rate anxiety on a scale of 0-10

Time frame
questionnaire given within 1 hour after regional anesthesia procedure
3

Pain Level Prior to Regional Anesthesia

questionnaire to rate pain on a scale of 0-10

Time frame
questionnaire given within 1 hour prior to regional anesthesia procedure
4

Pain Level During Regional Anesthesia

questionnaire to rate pain on a scale of 0-10

Time frame
questionnaire given within 1 hour after regional anesthesia procedure

Secondary outcomes

Other outcomes

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: