Brain Damage, Virtual Reality
Conditions
Brief summary
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
Interventions
DIAGNOSTIC_TESTVIRTUAL REALITY application
application on virtual reality headset
Sponsors
University Hospital, Angers
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Indication for brain lesion located in the right hemisphere surgery * Major patient * Karnofsky ≥ 70
Exclusion criteria
* Person with aphasia * Person with visual problems * Person with a contraindication to MRI * Person unable to carry out the tests planned in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Performance of the virtual reality application compared to classic cognitive tests batery for the detection of cognitive deficit | from surgery to 3 months after surgery |
Secondary
| Measure | Time frame |
|---|---|
| Performance of the virtual reality application compared with conventional cognitive tests used to detect facial emotion recognition disorders | 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 | 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 | from surgery to 3 months after surgery |
| Study the correlation between visuo-spatial and facial emotion recognition deficits and possible tractographic changes | 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 | from surgery to 3 months after surgery |
| Study the reproducibility of the virtual reality application for detecting the presence of cognitive function disorders | from surgery to 3 months after surgery |
Countries
France
Outcome results
None listed