Intensive Care specific Virtual Reality (ICU-VR) to improve psychological impairments in survivors of COVID-19

• Conditions: psychische klachten na IC opname, kwaliteit van leven; post-intensive care syndrome (PICS); PTSD; 10002861

• Registration Number: NL-OMON50036
• Lead Sponsor: Erasmus MC, Universitair Medisch Centrum Rotterdam

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 11 June 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 80

Inclusion Criteria

* * 18 years old
* A positive SARS-CoV-2 PCR with clinical signs of COVID-19 necessitating ICU
care
* Able to understand the Dutch language
* Signed informed-consent

Exclusion Criteria

* Documented active, established psychiatric disease (for instance personality
disorders or schizophrenia)
* Admitted with or a history of a primary neurological impairment necessitating
ICU admission to or discharge of the ICU (patients admitted with traumatic
brain injury, CVA, stroke, meningitis). Patients with a medical history of
delirium are eligible, if symptoms of delirium are not present at the time of
inclusion.
* Lack of formal home address

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The primary endpoint is the effect of ICU-VR after three months on the severity<br /><br>and occurrence of psychological sequelae and the HRQoL in ICU patients treated<br /><br>for COVID-19 up to 6 months after discharge. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>The secondary endpoint is the effect of ICU-VR after six months on the severity<br /><br>and occurrence of psychological sequelae and the HRQoL in ICU patients treated<br /><br>for COVID-19 up to 12 months after discharge.</p><br>