Neuropsychological Evaluation for Early Diagnosis of PSP

Sponsor
Ospedale Generale Di Zona Moriggia-Pelascini (Other)
Overall Status
Completed
CT.gov ID
NCT03478124
Collaborator
(none)
112
26

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Cognitive evaluation

Detailed Description

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 Design

Study Type:
Observational
Actual Enrollment :
112 participants
Observational Model:
Cohort
Time Perspective:
Other
Official Title:
The Role of the Neuropsychological Evaluation for Early Diagnosis of Progressive Supranuclear Palsy
Actual Study Start Date :
Jan 1, 2016
Actual Primary Completion Date :
Mar 1, 2018
Actual Study Completion Date :
Mar 2, 2018

Arms and Interventions

Arm Intervention/Treatment
PSP patients

Patients suffering from Progressive Supranuclear Palsy (PSP)

Behavioral: Cognitive evaluation
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.

PD Patients

Patients suffering from Parkinson's disease (PD)

Behavioral: Cognitive evaluation
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.

Outcome Measures

Primary Outcome Measures

  1. MMSE [1 year]

    Mini-Mental State Examination

  2. FAB [1 year]

    Frontal Assessment Battery

  3. MoCA [1 year]

    Montreal Cognitive Assessment

  4. WCST [1 year]

    Wisconsin Card Sorting Test

  5. ST [1 year]

    Stroop Test

  6. TMT-A and B [1 year]

    Trail Making Test Parts A & B

  7. VFT [1 year]

    Verbal fluency Test

  8. ROCF copy and delayed recall [1 year]

    Rey-Osterrieth complex figure test copy and delayed recall

  9. RAVLT [1 year]

    Rey Auditory Verbal Learning Test

Secondary Outcome Measures

  1. 6MWT [1 year]

    6 Minute Walk Test

  2. TUG [1 year]

    Timed Up and Go Test

  3. BBS [1 year]

    Berg Balance Scale

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Patients fulfilling the criteria for idiopathic PD

  • Patients fulfilling the criteria for PSP

Exclusion Criteria:
  • Any other neurodegenerative disorders or medical conditions different from PD / PSP

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Ospedale Generale Di Zona Moriggia-Pelascini

Investigators

  • Principal Investigator: Giuseppe Frazzitta, MD, Department of Parkinson's disease, Movement Disorders and Brain Injury Rehabilitation, "Moriggia-Pelascini" Hospital - Via Pelascini, 3, 22015, Gravedona ed Uniti, Como, Italy

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ospedale Generale Di Zona Moriggia-Pelascini
ClinicalTrials.gov Identifier:
NCT03478124
Other Study ID Numbers:
  • NPsy-PSP
First Posted:
Mar 27, 2018
Last Update Posted:
Mar 27, 2018
Last Verified:
Mar 1, 2018
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 27, 2018