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The purpose of this research study is to explore the impact of virtual reality (VR) on pain perception during out-patient procedures such as wart removal, wound debridement, and lidocaine injections.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Virtual Reality Group | Experimental | This group will receive the virtual reality intervention during out-patient bedside procedures. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Oculus Go Virtual Reality System | Other | The VR system will provide a 3D environment that provides distracting stimulus. Participant will put on the Oculus Go VR system headset 1-2 minutes prior to out-patient bedside procedure up to the completion of procedure which takes typically 3-5 minutes. |
| Measure | Description | Time Frame |
|---|---|---|
| Change in average pain as assessed by the visual analog scale (VAS) | VAS has a scoring range from 0 to 10 with 0 being no pain and 10 being the worst possible pain. | Baseline, up to 2 hours |
| Change in maximum pain level as assessed by VAS | VAS has a scoring range from 0 to 10 with 0 being no pain and 10 being the worst possible pain. | Baseline, up to 2 hours |
| Measure | Description | Time Frame |
|---|---|---|
| Change in heart rate | Heart rate will be assessed in beats per minute. | Baseline, up to 2 hours |
| Change in oxygen saturation | Oxygen saturation will be assessed as a percentage. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Hadar Lev-Tov, MD | University of Miami | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Miami | Miami | Florida | 33136 | United States |
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| ID | Term |
|---|---|
| D010146 | Pain |
| ID | Term |
|---|---|
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| Baseline, up to 2 hours |
| Incidence of intervention related adverse events | Intervention related adverse events will be assessed per treating physician discretion. | Baseline, up to 2 hours |