Walking memory tests may reveal early Parkinson's clues
NCT ID NCT07827963
First seen Sep 18, 2026 · Last updated Sep 18, 2026
Summary
Researchers are studying whether navigational memory fades before other spatial memory in people with Parkinson's disease and related conditions. The pilot includes 80 participants: those with mild or advanced Parkinson's, those with parkinsonism, and healthy volunteers. Participants complete memory tasks on foot and at a table while wearable sensors record their walking and eye-tracking glasses capture where they look. Assessments repeat at 12 and 24 months to see how memory, movement, and gaze relate over time.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- multimodal visuospatial and topographical memory assessment
- What this could lead to
- If navigational memory declines earlier than other spatial memory, doctors could one day use simple walking-and-memory tests to spot Parkinson's progression sooner and tailor rehabilitation.
- What could go wrong
- This is a small observational pilot with 80 participants, so it can only suggest patterns, not prove cause or predict individual outcomes. The findings may not apply to all people with Parkinson's or parkinsonism.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 80 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Oct 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients with Parkinson's disease, Parkinsonism, and healthy participants
- Ages
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35 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
3 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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IRCCS San Raffaele Cassino - CTC Via G. di Biasio, 1
Cassino, Frosinone, 03043, Italy
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University of Roma La Sapienza Department of Psychology University of Rome
Roma, Roma, 00185, Italy
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University of Roma La Sapienza Department of Psychology University of Rome 00185, Rome
Roma, Roma, 00185, Italy
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