Virtual Reality for ICU Delirium Prevention

Recruiting N/A Interventional Study
ICU Delirium
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
822 (estimated)
Sponsor
Cedars-Sinai Medical Center · Other
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About This Trial
The purpose of this study is to evaluate whether daily exposure to immersive virtual reality (VR) can reduce the incidence of delirium in high-risk, non-intubated ICU patients. Participants will be randomized to either standard ICU care or standard care plus once-daily 15-minute VR sessions consisting of calming natural scenes, guided meditation, and music. The study population includes adult surg…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Individuals who are currently admitted to the SICU at Cedars-Sinai Medical Center * Expected ICU stay \>48 hours * Richmond Agitation Sedation Scale (RASS) score between -1 to +2. * CAM-ICU negative * 1≤ risk factor for delirium (Age ≥ 65 years old, history of cognitive impair…
Contacts

Devon S Callahan, MD

310-423-2402

devon.callahan@cshs.org

CONTACT