Using virtual reality to reduce delirium in ICU patients

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial investigates the effectiveness of a Virtual Reality-based Family Support System (VRFS) in reducing delirium among mechanically ventilated patients in the ICU. Participants will be fitted with VR headsets and noise-canceling headphones to create a calming environment while allowing family members to provide support. The study will monitor physiological data and track delirium occurrences, sedative use, and ICU stay duration to assess the impact of the VR intervention on clinical outcomes.

Why it matters

Who can join: the full rules

Inclusion Criteria

* 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;
* Language: Chinese. Exclusion Criteria
* Severe visual or auditory impairments (diplopia, low vision due to macular degeneration, retinopathy; severe hearing loss or deafness);
* Cognitive and consciousness disturbances prior to ICU admission;
* Severe motion sickness;
* Head trauma or surgery that prevents the wearing of equipment;
* A history of long-term use of antipsychotic and/or benzodiazepine medications.

Where it's running

• Pumc
  Beijing, Beijing Municipality, China Recruiting

Study contacts

• Study coordinator: Yingying Yang, MD
• Email: yangyingying2703@outlook.com
• Phone: +8618800173833

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.