An interventional study of VIRTUAL REALITY application in Virtual Reality and Brain Damage, sponsored by University Hospital, Angers. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-07-30.
Sponsored by University Hospital, Angers · Not applicable, Interventional, and Diagnostic
Evaluate the diagnostic performance of a virtual reality application to detect the presence of cognitive impairment of the non-dominant hemisphere in patients with brain damage
2,112 studies on the registry are indexed under Brain Injuries; 384 are open to participants now.
This study's enrollment of 41 is below the median of 48 across 1,331 interventional studies indexed under Brain Injuries.
Browse Brain Injuries studies →University Hospital, Angers is the lead sponsor of 464 studies on the registry; 116 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Diagnostic Test: VIRTUAL REALITY application
application on virtual reality headset
Performance of the virtual reality application compared to classic cognitive tests batery for the detection of cognitive deficit
Time frame: from surgery to 3 months after surgery
Performance of the virtual reality application compared with conventional cognitive tests used to detect visual-spatial attention disorders
Time frame: from surgery to 3 months after surgery
Performance of the virtual reality application compared with conventional cognitive tests used to detect facial emotion recognition disorders
Time frame: from surgery to 3 months after surgery
Performance of the virtual reality application compared with conventional cognitive tests, used to detect spatial attention disorders or the presence of facial emotion recognition disorders depending respectively on the location or type of facial emotion
Time frame: from surgery to 3 months after surgery
Study the reproducibility of the virtual reality application for detecting the presence of cognitive function disorders
Time frame: from surgery to 3 months after surgery
Study the correlation between visuo-spatial and facial emotion recognition deficits and possible tractographic changes
Time frame: from surgery to 3 months after surgery
Study the association between the presence of cognitive function deficits and the presence of behavioral disorders or health-related quality of life
Time frame: from surgery to 3 months after surgery
Plan to share: No
No publications or documents are linked to this record.
This study is completed, as verified in Jul 2025. You cannot join it, but the record below documents what was studied.
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University Hospital, Angers