Effects of Multi-model Virtual Reality Intervention Method to Reduce the Prevalence of Delirium in ICU Patients with Mechanical Ventilation

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to learn the effect of VR-based Family Support System (VRFS) on reducing delirium in ICU mechanically ventilated patients. The main question it aims to answer is: ·Using VRFS for participant intervention, can it reduce the incidence of delirium and improve clinical outcomes? Researchers will investigate whether the implementation of VRFS can reduce the number of delirium days and improve clinical outcomes. Participants will: * Receive the VRFS intervention until the endotracheal tube (ETT) is removed. * Have physiological data collected, including EEG, oxygen saturation levels, ECG, and blood pressure. * Keep a diary of delirium, dosage of sedative and analgesic drugs, the duration of mechanical ventilation, and ICU stays.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 90
Healthy Volunteers: f
View:

• Mechanical ventilation duration is expected to be greater than 24 hours;

• ICU stay duration is expected to be greater than 72 hours;

• Age is 18 years or older, with no upper age limit;

Locations
Other Locations
China
PUMC
RECRUITING
Beijing
Contact Information
Primary
Yingying Yang, MD
yangyingying2703@outlook.com
+8618800173833
Time Frame
Start Date: 2023-12-18
Estimated Completion Date: 2026-12-31
Participants
Target number of participants: 102
Treatments
Experimental: VRFS Intervention
Participants will receive standard ICU care and will also undergo VRFS intervention.
No_intervention: Standard ICU Care
Patients will be treated with standard ICU care and not receive VR stimulation.
Related Therapeutic Areas
Sponsors
Leads: Peking Union Medical College Hospital

This content was sourced from clinicaltrials.gov