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RECRUITINGINTERVENTIONAL

Virtual Reality Devices as an Adjunct to Usual Care for Patients With Sickle Cell Disease Experiencing Vaso-Occlusive Crises

Pilot Study to Investigate the Use of Virtual Reality Devices as an Adjunct to Usual Care for Patients With Sickle Cell Disease Experiencing Vaso-Occlusive Crises

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

This study aims to evaluate the use of virtual reality as an adjunct to standard care for patients with sickle cell disease experiencing vaso-occlusive crises.

Who May Be Eligible (Plain English)

Who May Qualify: - Adult (age \> 18 years) emergency department patient - History of sickle cell disease - Presenting to the emergency department due to acute pain related to sickle cell disease thought to be due to vaso-occlusive crisis Who Should NOT Join This Trial: - Prior enrollment in this study - Presenting with a chief complaint suggestive of a complicated crisis (such as concern for acute chest syndrome, splenic sequestration, hepatic sequestration, pulmonary embolism) as determined by the clinical care provider - Not being treated with intravenous opioids for the vaso-occlusive crisis - Patients who lack the capacity to provide willing to sign a consent form - Medical history of seizures or known intolerance to virtual reality - Disabilities like vision and hearing defects etc. that preclude the use of a head mounted virtual reality device. - Known to be pregnant - Incarcerated at the time of evaluation - Over the age of 89 years old Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Adult (age \> 18 years) emergency department patient * History of sickle cell disease * Presenting to the emergency department due to acute pain related to sickle cell disease thought to be due to vaso-occlusive crisis Exclusion Criteria: * Prior enrollment in this study * Presenting with a chief complaint suggestive of a complicated crisis (such as concern for acute chest syndrome, splenic sequestration, hepatic sequestration, pulmonary embolism) as determined by the clinical care provider * Not being treated with intravenous opioids for the vaso-occlusive crisis * Patients who lack the capacity to provide informed consent * Medical history of seizures or known intolerance to virtual reality * Disabilities like vision and hearing defects etc. that preclude the use of a head mounted virtual reality device. * Known to be pregnant * Incarcerated at the time of evaluation * Over the age of 89 years old

Treatments Being Tested

DEVICE

Virtual Reality Headset and Hand-Held Controllers

Study Group-Virtual reality headset and hand-held controllers will be used as an adjuvant to pain management care.

OTHER

Blindfolding and Noise Cancelling

Control group-Blindfold and noise cancelling headphones will be a placebo comparator group to the experimental interventions of virtual reality devices.

Locations (1)

University of Maryland Medical Systems
Baltimore, Maryland, United States