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RECRUITING
NCT07357389
NA

Virtual Reality for ICU Delirium Prevention

Sponsor: Cedars-Sinai Medical Center

View on ClinicalTrials.gov

Summary

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 surgical ICU patients at Cedars-Sinai who are CAM-ICU negative at enrollment and possess at least one established risk factor for delirium. Outcomes will include the incidence and duration of delirium, ICU and hospital length of stay, feasibility of the VR intervention, and the frequency of adverse events. By targeting a high-risk population with an innovative non-pharmacologic therapy, this trial aims to generate data to support integration of VR into ICU delirium prevention protocols.

Official title: VR for ICU Delirium Prevention

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

822

Start Date

2026-03-10

Completion Date

2028-04

Last Updated

2026-03-17

Healthy Volunteers

Yes

Conditions

Interventions

DEVICE

Virtual Reality therapeutics

Patients will receive daily VR sessions for up to 5 days in addition to regular delirium prevention measures in the ICU

Locations (1)

Cedars Sinai Medical Center

Los Angeles, California, United States