VIrtual Reality Glasses Use to Improve Lateropulsion and the Post-stroke Postural Vertical
VIrtual Reality Glasses Use to Improve Lateropulsion and the Post-stroke Postural Vertical (VIRGIL)
University Hospital, Grenoble
40 participants
Jun 15, 2021
INTERVENTIONAL
Conditions
Summary
VIRGIL is a monocentric interventional study aiming to investigate the effect of immersion in a virtual tilted room on modulation of the verticality representation (postural vertical \[PV\] and visual vertical \[VV\]), which in turn might affect body orientation (head and trunk). To this end, the investigators will conduct a within-person randomized trial including post-stroke patients and healthy participants.
Eligibility
Inclusion Criteria9
- stroke participants
- Hospitalized in neurorehabilitation
- Hemisphere stroke (Right or left)
- Stroke delay \< 6 months
- Presence of lateropulsion assessed by the Scale for Contraversive Pushing (SCP) \> 0.5
- healthy participants
- No history of stroke or others neurological pathologies
- No balance disorders
- No history of vestibular or dizzissness disorders
Exclusion Criteria12
- All
- History of psychiatric disorders
- Nyctophobia
- Advanced heart failure
- Severe trunk deformation with C7 lateral \> 30 mm due to a independant cause beyond the stroke (i.e., scoliosis) or history of postural disorder
- Stroke participants
- Medical instability making the assessment impossible
- Comprehension deficits with Boston Diagnostic Aphasia Examination gravity score ≥3
- History of vestibular or dizzissness disorders
- No previous neurological history interfering with balance
- Inability to understand and execute simple orders
- Severe untreated depression (Aphasic Depression Rating Scale (ADRS) score \>15)
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Interventions
The immersion in virtual reality will be based on the HTC VIVE® device and the software developed by the Virtualis Society.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT04911738