The aim of this study is to better understand the nature of the cognitive decline in Progressive Supranuclear Palsy, the time of its development and the relation with the other cardinal features of the disease.
Progressive Supranuclear Palsy (PSP) is a neurodegenerative disease characterized by vertical supranuclear gaze palsy, early balance dysfunction and falls. Tau-protein aggregation, mainly in the brainstem, is the disease hallmark. Because of the similarities with Parkinson's disease (PD), the diagnosis is made approximately 4 years after the symptoms onset. Cognitive deficits are a leading feature of PSP and they actually represent one of the four functional core domains in the revised diagnostic criteria. The aim of this study is to better understand the nature of this cognitive decline, the time of its development and the relation with the other cardinal features of the disease.
Study Type
OBSERVATIONAL
Enrollment
112
An extensive battery of neuropsychological and motor tests was assessed: MMSE, FAB, MoCA, WCST, Stroop Test, TMT-A and B, Verbal fluency Test, ROCF copy and delayed recall, RAVLT, 6MWT, TUG, BBS.
MMSE
Mini-Mental State Examination
Time frame: 1 year
FAB
Frontal Assessment Battery
Time frame: 1 year
MoCA
Montreal Cognitive Assessment
Time frame: 1 year
WCST
Wisconsin Card Sorting Test
Time frame: 1 year
ST
Stroop Test
Time frame: 1 year
TMT-A and B
Trail Making Test Parts A \& B
Time frame: 1 year
VFT
Verbal fluency Test
Time frame: 1 year
ROCF copy and delayed recall
Rey-Osterrieth complex figure test copy and delayed recall
Time frame: 1 year
RAVLT
Rey Auditory Verbal Learning Test
Time frame: 1 year
6MWT
6 Minute Walk Test
Time frame: 1 year
TUG
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Timed Up and Go Test
Time frame: 1 year
BBS
Berg Balance Scale
Time frame: 1 year