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

Description

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.

Conditions

Sickle Cell Disease, Vaso-occlusive Pain Episode in Sickle Cell Disease, Acute Pain

Study Overview

Study Details

Study overview

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.

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

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

Condition
Sickle Cell Disease
Intervention / Treatment

-

Contacts and Locations

Baltimore

University of Maryland Medical Systems, Baltimore, Maryland, United States, 21201

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility 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
  • * 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

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Maryland, Baltimore,

R. Gentry Wilklerson, MD, PRINCIPAL_INVESTIGATOR, U of Maryland, Baltimore

Study Record Dates

2025-12-31