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Gait Characteristics and Cognitive Evolution in Parkinson Disease

Completed
Conditions
Parkinson's Disease
Registration Number
NCT04297800
Lead Sponsor
FROM- Fondazione per la Ricerca Ospedale di Bergamo- ETS
Brief Summary

Parkinson's disease (PD) is a chronic progressive nervous system disease with gradual motor impairment. Cognitive dysfunction is common in PD, even in the early stages, and it is characterized by impairments in executive, attention, memory, language and visuospatial function. Motor symptoms, in particular, alterations in gait, have been studied in clinical practice to assess disease progression, and its response to treatments, both farmacological and physiotherapeutic.

Recent research on wearable technology in PD has shown that motor tests can be automated using wearable technology to eliminate human supervision and patient-reported data. Particularly, the quantitative gait analysis by using inertial devices has been proposed as a sensitive tool to longitudinally monitor gait worsening, response to dopaminergic treatment over time and cognitive dysfunction in PD patients.

The aim of this prospective multicente observational study is to investigate whether the dysfunction of specific gait parameters may be correlated to cognitive impairment (Attention/Executive Function Domain) in a cohort of ambulatory PD patients followed for 3 years.

Detailed Description

This is a prospective multicenter observational study with annual follow-up assessments over 3 years.

Gait is assessed by an inertial device (BTS G-WALK). G- WALK is an easy-to-use solution to obtain accurate, objective and quantitative spatial-temporal gait data. The device is a wireless system consisting of an inertial sensor composed by a triaxial accelerometer, a magnetic sensor, and a triaxial gyroscope that positioned on lumbar/ or sacral segments allows a functional gait analysis.

Cognitive performance is evaluated with a neuropsychological battery designed to assess memory, executive /attention, and visuospatial domains.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Both sex
  • Aged between 55-74 years
  • Diagnosis of idiopathic PD based on MDS clinical diagnostic criteria
  • Hoehn & Yahr (H&Y) stages 2 to 3 at enrollment, independently by PD duration
  • Clinical-pharmacological stabilization until 3 months before the enrollment
  • DBS treatment (stable stimulation parameters until 6 months before the enrollment)
Exclusion Criteria
  • Evidence of neurodegenerative and secondary parkinsonism
  • Dementia ( (score <25 on the Mini Mental State Examination - MMSE)
  • Psychiatric disorder (Beck Depression Inventory-II - BDI-II Score >19)
  • Presence of organ failure (Modified Cumulative Illness Rating Scale - CIRS > 2)
  • Orthopedic disorder or co-morbidities that may affect gait
  • Drug and alcohol use

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Changes in Gait assessed by 6-Minute Walk Test (6MWT)Every year for 3 years

Gait assessment

Changes in Gait assessed by Extended-Time Up and Go (eTUG)Every year for 3 years

Gait assessment

Changes in cognitive function assessed by Mini-Mental State Examination (MMSE)Every year for 3 years

Cognitive Assessment. The MMSE score ranges from 0 to 30 points, in which a lower score indicates a higher degree of cognitive impairment.

Changes in cognitive function assessed by the Montreal Cognitive Assessment (MoCA)Every year for 3 years

Cognitive Assessment. The total score of the MoCA is 30 points, with a score less than 24 is considered cognitive impairment.

Changes in cognitive function assessed by Frontal Assessment Battery (FAB)Every year for 3 years

Cognitive Assessment

Secondary Outcome Measures
NameTimeMethod
Movement Disorder Society-Unified Parkinson&#39;s Disease Rating Scale, part IIIEvery year for 3 years

The MDS-UPDRS III is the sum of 33 scores that evaluate Parkinson\&#39;s disease motor symptoms on a scale from 0 to 4 points. The total scale range is 0-132, where higher scores indicate more severe symptoms.

&#34;Rapid eye movement Sleep&#34; Behavior Disorder Screening QuestionnaireEvery year for 3 years

The RBDSQ ranges from 0 to 13, where higher scores represent a worse outcome.

Hyposmia Rating ScaleEvery year for 3 years

The scale ranges from 6 to 24, where higer scores indicate more worse sense of olfaction.

short Falls Efficacy ScaleEvery year for 3 years

s-FES ranges from 7 to 28, where higher scores indicate high level of concern about falling during social and physical activities inside and outside the home.

Berg Balance ScaleEvery year for 3 years

The BBC includes 14 functional balance. The scale ranges from 0 to 56, where higer scores indicate that the participant can complete the tasks.

Tinetti testEvery year for 3 years

The test grants a maximum of 16 points for static part (sitting) and 12 point for dynamic (walking) part. Higher is the score, better is the performance

Parkinson's Disease QuestionnaireEvery year for 3 years

PDQ-8 ranges from 0 to 32, where higher scores reflect a lower health-related quality of life.

Beck Anxiety IndexEvery year for 3 years

The BAI range is 0- 63, where higer scores indicate more severe symptoms.

Beck Depression Inventory IIEvery year for 3 years

The BDI-II ranges from 0 to 63, where higer scores indicate more severe depressive symptoms.

Trial Locations

Locations (3)

ASST- Papa Giovanni XXIII

🇮🇹

Bergamo, Italy

Spedali Civili di Brescia

🇮🇹

Brescia, Italy

Ospedale San Gerardo di Monza

🇮🇹

Monza, Italy

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