Tiny brain clues may reveal how dementias differ
NCT ID NCT06354933
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study examined 186 people with Alzheimer's, Lewy body, frontotemporal, or corticobasal dementia, plus healthy controls, to see if subtle physical signs (like coordination or reflexes) differ between dementia types. Participants had simple exams and cognitive tests. The goal was to better understand how these diseases affect the brain, not to test a treatment.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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186 people
The number who actually took part.
- Started
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Apr 2022
- Finished
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Feb 2024
- 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
The study will include individuals diagnosed with Alzheimer's Disease (AD), Frontotemporal Dementia (FTD), Corticobasal Syndrome (CBS), or Lewy Body Dementia (LBD), along with age and gender-matched controls without dementia. Controls will be recruited from caregivers and companions of patients attending other neurological clinics. All participants will undergo thorough neurological and neuropsychiatric assessments to confirm eligibility and evaluate outcomes.
- Ages
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18 years and older
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Diagnosis of probable Alzheimer's Disease (AD), Frontotemporal Dementia (FTD), Corticobasal Syndrome (CBS), or probable Lewy Body Dementia (LBD) according to established clinical criteria. * MMSE score greater than 10. * Age and gender-matched controls without a history of neurological or psychiatric conditions. Exclusion Criteria: * Mixed dementia or vascular etiology. * History of neurological or psychiatric conditions predating the dementia diagnosis. * Substance or alcohol abuse history. * Known comorbidities affecting neurological or psychiatric function. * MMSE score less than or equal to 10. * Inability to provide informed consent.
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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.
Contacts and locations
Locations
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Fondazione IRCCS San Gerardo dei Tintori
Monza, Lombardy, 20900, Italy
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Other studies related to the condition(s) this trial covers.
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