Evaluation of a Virtual Reality Tool for Identifying the Cognitive Functions of the Right Hemisphere in Patients With Brain Damage -TANGO

Not Applicable

Completed

• Conditions: Virtual Reality; Brain Damage

• Registration Number: NCT04288505
• Lead Sponsor: University Hospital, Angers

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

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2020-02-14
• Study First Submitted QC: 2020-02-25
• Study First Posted: 2020-02-28
• Study Start: 2020-05-15
• Primary Completion: 2025-02-04
• Study Completion: 2025-05-05
• Status Verified: 2025-07
• Last Update Submitted: 2025-07-25
• Last Update Posted: 2025-07-30

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 41

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
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
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 visual-spatial attention 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
Study the reproducibility of the virtual reality application for detecting the presence of cognitive function 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

Trial Locations

Locations (1)

University hospital; 🇫🇷 Angers, France