Progression of Striatal and Extrastriatal Degeneration in PD and PSP Patients
NCT ID: NCT03840252
Last Updated: 2024-04-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
78 participants
INTERVENTIONAL
2015-09-23
2019-07-31
Brief Summary
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Specifically, this study want to identify cognitive pattern and gait-related cerebral diffusion/functional connectivity in PD and PSP patients and to verify their progression over a period of 18 months.
In summary, the current protocol proposed to investigate the following issues:
* to perform a multifactorial quantitative analysis of outcomes for PD and PSP compared to a control group in order to categorize cognitive and gait pattern in the group of patients and verify if the gait can be useful as discriminator for diagnosis.
* to analyze whether diffusion and resting-state functional connectivity indices are correlated with clinical disease severity scores and motor scores and how they change over time (18 months later).
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Detailed Description
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At the same time, emerging evidence indicates that early disturbances in cognitive processes such as attention, executive function, and working memory are associated with slower gait and gait instability during single and dual-task testing.
It is therefore crucial to carefully investigate the multiple cognitive domains in order to identify possible mild cognitive deficits in PD and PSP patients and to correlate them with gait disorders.
The use of quantitative movement analysis with 3D-gait analysis allow an objective multifactorial evaluation of the functional limitation related to PD and PSP patients and can be used to analyze the gait in pathologies characterized by gait impairment compared to healthy control (HC).
This longitudinal clinical study aims to analyze cognitive profiles and gait pattern (with 3D-gait analysis) and their progression (18 months later) in a PD- and a PSP-group, respect to HC group.
Moreover, with the Magnetic Resonance Imaging (MRI), the study want to research for possible gait-related cerebral diffusion/functional connectivity alterations and their changes over time.
The specific aims of the project are:
* To perform a multifactorial quantitative analysis of outcomes for PD and PSP compared to a control group in order to categorize the gait in the group of patients and verify if the gait can be useful as discriminator for diagnosis.
* To detect possible cognitive deficits in Parkinson's Disease and PSP more corelated with gait disturbances.
* To analyze whether diffusion and resting-state functional connectivity indices are correlated with clinical disease severity scores and motor scores and how they change over time (18 months later).
* To identify gait-related cerebral diffusion/functional connectivity in PD and PSP patients and to verify their progression over a period of 18 months.
Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
DIAGNOSTIC
NONE
Study Groups
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PD patients: Parkinson's disease group
Diagnosis of idiopathic PD by United Kingdom Brain Bank criteria, exclusion of other significant neurological or orthopedic problems; ages of 21-90; able to walk 25 feet unassisted and without any assistive device.
Imaging: rsfMRI, diffusion tensor imaging; Motor evaluation: 3D gait analysis; Movement Disorder Society (MDS)-UPDRS Behavioral: PD-MCI-specific Level II battery (Mov Dis. 2015 Mar; 30(3): 402-406)
3D gait analysis
Computed analysis of posture and gait pattern and motor performance by kinematic and kinetics parameters analysis such as the step length, gait velocity, stride time variability, 3D joint kinematics, ground reaction forces, joint kinetics
rsfMRI
MR scans acquired by 1.5 Tesla (Siemens Medical Systems, Erlangen, Germany).
Montreal Cognitive assesment (MoCA)
Standard clinical questionnaire
PSP patients
Application of the National Institute of Neurological Disorders and Stroke and Society for Progressive Supranuclear Palsy (NINDS-SPSP) criteria for the clinical diagnosis of "probable" PSP, evaluation of PSP rating scale, exclusion of other significant neurological or orthopedic problems; ages of 21-90; able to walk 25 feet unassisted and without any assistive device.
Imaging: rsfMRI, diffusion tensor imaging; Motor evaluation: 3D gait analysis;MDS-UPDRS Behavioral: PD-MCI-specific Level II battery (Mov Dis. 2015 Mar; 30(3): 402-406)
3D gait analysis
Computed analysis of posture and gait pattern and motor performance by kinematic and kinetics parameters analysis such as the step length, gait velocity, stride time variability, 3D joint kinematics, ground reaction forces, joint kinetics
rsfMRI
MR scans acquired by 1.5 Tesla (Siemens Medical Systems, Erlangen, Germany).
Montreal Cognitive assesment (MoCA)
Standard clinical questionnaire
HC: healthy control group
Healthy adults ages 21-90 without movement disorders, psychiatric disorders, or dementia.
Imaging: rsfMRI, diffusion tensor imaging; Motor evaluation: 3D gait analysis; Behavioral: PD-Mild Cognitive Impairment (MCI)-specific Level II battery (Mov Dis. 2015 Mar; 30(3): 402-406)
3D gait analysis
Computed analysis of posture and gait pattern and motor performance by kinematic and kinetics parameters analysis such as the step length, gait velocity, stride time variability, 3D joint kinematics, ground reaction forces, joint kinetics
rsfMRI
MR scans acquired by 1.5 Tesla (Siemens Medical Systems, Erlangen, Germany).
Montreal Cognitive assesment (MoCA)
Standard clinical questionnaire
Interventions
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3D gait analysis
Computed analysis of posture and gait pattern and motor performance by kinematic and kinetics parameters analysis such as the step length, gait velocity, stride time variability, 3D joint kinematics, ground reaction forces, joint kinetics
rsfMRI
MR scans acquired by 1.5 Tesla (Siemens Medical Systems, Erlangen, Germany).
Montreal Cognitive assesment (MoCA)
Standard clinical questionnaire
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* ages of 20-80;
* able to walk 25 feet unassisted and without any assistive device
Exclusion Criteria
* Cardiac pacemaker implantation
20 Years
80 Years
ALL
Yes
Sponsors
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IRCCS San Raffaele Roma
OTHER
Responsible Party
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Principal Investigators
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Fabrizio Stocchi, MD, PhD
Role: STUDY_DIRECTOR
IRCCS San Raffaele Pisana
Locations
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Casa di cura San Raffaele Cassino
Cassino, Frosinone, Italy
Countries
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Other Identifiers
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RP 06/15
Identifier Type: -
Identifier Source: org_study_id
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