Investigating Visuo-spatial Abilities and Psychological Effects in West Nile and Multiple Sclerosis Patients with a Focus on a Possible Rehabilitation Protocol
Recruiting · NCT06640660 · Interventional (participants receive a specific treatment) · Lead sponsor: IRCCS San Camillo, Venezia, Italy
View the official record on ClinicalTrials.gov →Interventions studied
Conventional rehabilitationMindlenses Professional
What this trial is about
The study aims to investigate visuospatial abilities and psychological outcomes in patients with multiple scleroris (MS) and patients with West Nile virus infection (vWN). Patients will undergo a specific neuropsychological and psychological evaluation. Afterwards, patients will receive 10 sessions of cognitive training integrating digital exercises and prismatic lenses. At the end of the treatment, patients will be re-evaluated to explore for potential changes in the cognitive and psychological profile.
Who can take part
Age range
20 Years to 85 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Diagnosis of: Multiple Scleroris OR vWN infection ascertained by laboratory analysis and received no later than twelve months prior to the date of hospitalization
- preserved use of at least one hand
- normal or corrected to normal vision
Exclusion criteria
- history of psychiatric and/or concurrent neurological diseases
- inability to provide informed consent,
- impaired comprehension of oral instructions,
Where it is running
1 location listed.
- IRCCS San Camillo Hospital - Lido, Venezia, Italy