Clinical Trials in Italy / NCT07827963
Starting soon Observational

VisMemoPD Protocol: an Observational Pilot Study on Spatial and Topographical Memory in Patients With Parkinson's Disease and Parkinsonism

NCT07827963 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2026-09
Last updated
2026-09-18

Condition(s) studied

Parkinson's DiseaseParkinsonismMultiple System AtrophyProgressive Supranuclear PalsyMild Cognitive Impairment

Investigational drug(s) / intervention(s)

Multimodal visuospatial and topographical memory assessment

Multimodal visuospatial and topographical memory assessment: Participants will undergo visuospatial memory assessment using the Corsi Block-Tapping Test and topographical memory assessment using the Walking Corsi Test. Gait parameters will be recorded using wearable inertial sensors, while visual exploration strategies will be assessed using a wearable eye-tracking system. Assessments will be performed at baseline and repeated at 12 and 24 months.

Study summary

VISMEMO-PD is an observational pilot study aimed at investigating visuospatial memory in reaching space and topographical memory in navigational space in patients with Parkinson's disease and Parkinsonism. The protocol is based on the hypothesis that topographical memory may deteriorate before visuospatial memory, suggesting that navigational memory impairment could represent an early indicator of disease progression. The study will include 80 participants stratified into four groups: patients with mild Parkinson's disease, patients with moderate-advanced Parkinson's disease, patients with Parkinsonism, and healthy participants. Visuospatial memory will be assessed using the Corsi Block-tapping Test, while topographical memory will be assessed using the Walking Corsi Test. Walking motor patterns will be recorded using wearable inertial sensors from the MOVIT system, and visual exploration strategies will be assessed using a wearable Pupil Labs eye-tracking system. The integration of cognitive, motor, and eye-tracking measures may support the identification of early neuropsychological markers and the development of tailored neurorehabilitation pathways for individuals with Parkinson's disease and Parkinsonism.

Eligibility

Sex
ALL
Min age
35 Years
Max age
80 Years
Healthy volunteers
Accepted
Inclusion Criteria * Male and female subjects aged between 35 and 80 years; * Diagnosis of Parkinson's disease according to the United Kingdom (UK) Parkinson's Disease Society Brain Bank criteria; * Diagnosis of primary atypical parkinsonism MSA-P, according to the Second Consensus Statement on the Diagnosis of Multiple System Atrophy; * Diagnosis of primary atypical parkinsonism PSP-P, according to the Movement Disorder Society criteria for Progressive Supranuclear Palsy; * Modified Hoehn and Yahr stage between 1 and 3 during the "ON" phase (Hoehn and Yahr, 1967); * Cognitive screening with the Montreal Cognitive Assessment (MoCA) score \> 17; * Mini-Mental State Examination (MMSE) score ≥ 24 (Folstein et al., 1975); * Ability to walk independently for 10 meters without assistive devices; * Ability to understand and sign the informed consent form; * Ability to comply with study procedures. Exclusion Criteria * Diagnosis of neurological disorders other than Multiple System Atrophy (MSA) and Parkinson's disease; * Depressive disorders or Beck Depression Inventory-II (BDI-II) score \> 20; * Musculoskeletal disorders that could impair gait performance. The study will enroll 20 healthy subjects, matched by age and sex with patients affected by Parkinson's disease (PD) and atypical parkinsonism who will be recruited into the study. The same inclusion criteria will be applied to both groups of patients with Multiple System Atrophy (MSA) and Parkinson's disease. The exclusion criteria will be: * Diagnosis of neurological disorders; * Depressive disorders or Beck Depression Inventory-II (BDI-II) score \> 20; * Musculoskeletal disorders that could impair gait performance.

Primary outcome measure(s)

Trial sites (3)

FacilityCityRegionStatus
IRCCS San Raffaele Cassino - CTC Via G. di Biasio, 1 Cassino Frosinone
University of Roma La Sapienza Department of Psychology University of Rome 00185, Rome Roma Roma
University of Roma La Sapienza Department of Psychology University of Rome Roma Roma

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07827963 on ClinicalTrials.gov ↗ ← All trials in Italy