Combining tDCS with prismatic adaptation for non-invasive neuromodulation of the motor cortex.
Martina Bracco, Giuseppa Renata Mangano, Patrizia Turriziani...
https://pubmed.ncbi.nlm.nih.gov/28487249Actively Recruiting
Led by IRCCS San Camillo, Venezia, Italy · Updated on 2024-10-15
50
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are studying visuospatial abilities and psychological outcomes in patients with Multiple Sclerosis (MS) and West Nile virus infection (vWN). Both conditions can affect cognitive functions such as attention, memory, and executive skills. This study aims to better understand these impairments and test a new rehabilitation approach to improve visuospatial and cognitive functions. Participants will receive 10 sessions over 2 weeks of cognitive training using Mindlenses Professional, a device that combines prismatic adaptation therapy with digital serious games targeting attention, executive functions, and language. There is also a comparison group receiving standard computerized cognitive rehabilitation offered by the hospital. During the study, patients will undergo neuropsychological and psychological evaluations before and after the treatment to assess changes in cognitive performance and psychological status. The primary outcome measures cognitive changes after the 2-week intervention, while secondary outcomes assess psychological effects. The study involves randomized assignment and single masking, with a total participation period of about 2 weeks.
CONDITIONS
Investigating Visuo-spatial Abilities and Psychological Effects in West Nile and Multiple Sclerosis Patients with a Focus on a Possible Rehabilitation Protocol
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Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 2 weeks
Participants undergo 2 weeks of cognitive rehabilitation. The experimental group uses Mindlenses Professional combining prismatic adaptation and serious games focused on attention, executive functions, and language. The control group performs standard cognitive training.
10 sessions over 2 weeks
Duration - Immediately after treatment (post-intervention)
Participants are assessed for changes in cognitive performance and psychological aspects after the treatment.
1 visit (in-person)
Total: 1 location
1
IRCCS San Camillo Hospital
Lido, Venezia, Italy, 30126
Actively Recruiting
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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