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Gait Characteristics and Cognitive Evolution in Parkinson Disease (GECO-PD)

F

FROM- Fondazione per la Ricerca Ospedale di Bergamo- ETS

Status

Completed

Conditions

Parkinson's Disease

Study type

Observational

Funder types

Other

Identifiers

NCT04297800
GECO-PARKINSON STUDY

Details and patient eligibility

About

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.

Full 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.

Enrollment

60 patients

Sex

All

Ages

55 to 74 years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

3

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Central trial contact

Dario Alimonti, MD, PhD; Rosalia Zangari, PhD

Data sourced from clinicaltrials.gov

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