Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06184126

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

Led by University of Maryland, Baltimore · Updated on 2025-12-24

30

Participants Needed

1

Research Sites

112 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult emergency department patient aged over 18 years
  • History of sickle cell disease
  • Presenting to the emergency department with acute pain related to sickle cell disease thought to be due to vaso-occlusive crisis
Not Eligible

You will not qualify if you...

  • Prior enrollment in this study
  • Presenting with a complicated crisis (such as acute chest syndrome, splenic or hepatic sequestration, pulmonary embolism) as determined by clinical care provider
  • Not receiving intravenous opioids for the vaso-occlusive crisis
  • Lacking capacity to provide informed consent
  • Medical history of seizures or known intolerance to virtual reality
  • Disabilities like vision or hearing defects preventing use of virtual reality headset
  • Known pregnancy
  • Currently incarcerated
  • Over 89 years old

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Maryland Medical Systems

Baltimore, Maryland, United States, 21201

Actively Recruiting

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Research Team

R

R. Gentry Wilkerson, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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