FAME: A Italian test to recognize famous faces and name them
Official title: Sviluppo, Validazione e Dati Normativi Della Batteria Italiana Per il Riconoscimento Dei Volti Famosi I-FACE
Run by Istituti Clinici Scientifici Maugeri SpA · NCT07911878 · Data updated 2026-11-12
This project tests an Italian battery to see how well people with stroke or neurodegenerative diseases recognize famous faces and recall their names, familiarity, and related facts.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 40 Years to 85 Years |
| Sex | All |
| Enrollment | 300 (estimated) |
| Sponsor | Istituti Clinici Scientifici Maugeri SpA Academic / other |
| Locations | 10 sites (Sciacca, AG and 9 other locations) |
| Status | Recruiting |
| Started | September 5, 2025 |
| Main results expected | January 31, 2028 |
| Study ends | September 30, 2028 |
| Registry record updated | November 3, 2026 |
| Trial ID | NCT07911878 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults aged 40–85, including healthy controls and patients with frontotemporal dementia, Alzheimer’s disease, or stroke who can provide informed consent and have adequate vision and hearing.
✕Probably not a fit
Patients with severe sensory impairment or non-Italian speakers may not benefit from this battery.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The I-FACE project develops and validates a comprehensive neuropsychological battery to assess famous-face recognition in individuals with neurodegenerative diseases and stroke. It covers three components—familiarity, semantic knowledge, and naming—and includes four tasks to measure these abilities. A pilot study will refine items and ensure internal consistency, followed by collecting Italian normative data by age, sex, and education, and establishing cut-off scores. The battery will then be administered to people with frontotemporal dementia, Alzheimer's disease, and stroke to evaluate reliability and validity and its ability to distinguish impaired from unimpaired recognition. The study uses neuropsychological assessment as the primary intervention.
Why it matters
Potential benefit: If successful, clinicians will have a validated Italian tool to detect and quantify famous-face recognition difficulties, aiding diagnosis and care planning.
How similar studies have gone: Previous work in neuropsychological testing supports the feasibility of face-recognition batteries; this study adapts and validates such an approach for the Italian population and specific patient groups.
Who can join: the full rules
Show full inclusion / exclusion criteria
1. Healthy Controls (HC) Inclusion Criteria: Age 40-85 years. No chronic medical, neurological, or psychiatric conditions, or major depressive episode detected during screening. No history of schizophrenia or bipolar disorder in the 5 years prior to screening. Mini-Mental State Examination (MMSE) score ≥ 26. Exclusion Criteria: Uncorrected vision or hearing impairment. 2. Frontotemporal Dementia (FTD) Patients Inclusion Criteria: Diagnosis of probable FTD according to established clinical criteria. Age 40-85 years. Ability to provide informed consent. Exclusion Criteria: History of neurological diseases other than FTD (e.g., stroke, brain tumor, multiple sclerosis, traumatic brain injury). Uncorrected vision or hearing impairment. History of serious psychiatric diseases, developmental disorders (e.g., autism spectrum), or intellectual disability. Dementia severity (CDR) \> 1. 3. Alzheimer's Disease (AD) Patients Inclusion Criteria: Diagnosis of probable AD according to established clinical criteria. Age 40-85 years. Ability to provide informed consent. Exclusion Criteria: History of neurological diseases other than AD (e.g., stroke, brain tumor, multiple sclerosis, traumatic brain injury). Uncorrected vision or hearing impairment. History of serious psychiatric diseases, developmental disorders, or intellectual disability. Dementia severity (CDR) \> 1. 4. Post-Stroke Patients Inclusion Criteria: Subacute phase: 1 week to 3 months post-event. Ischemic or hemorrhagic stroke confirmed by neuroimaging and/or clinical judgment. Exclusion Criteria: History of previous stroke or multifocal stroke documented by imaging. Brainstem or cerebellar stroke. History of traumatic brain injury (TBI), seizures, brain tumors, neurodegenerative diseases, or psychiatric disorders.
Where it's running
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ICS Maugeri Sciacca
Sciacca, Ag, Italy Recruiting -
IRCCS Maugeri Lumezzane
Lumezzane, Bs, Italy Recruiting -
ICS Maugeri Mistretta
Mistretta, Me, Italy Recruiting -
IRCCS Maugeri Montescano
Montescano, Pv, Italy Recruiting -
Istituti Clinici Scientifici Maugeri IRCCS Bari
Bari, Italy Recruiting -
Istituti Clinici Scientifici Maugeri IRCCS Milano
Milan, Italy Recruiting
Show 4 more locations
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IRCCS Maugeri Pavia
Pavia, Italy Recruiting -
IRCCS Maugeri Telese Terme
Telese Terme, Italy Recruiting -
IRCCS Maugeri Castel Goffredo
Castel Goffredo, Mn, Italy Not yet recruiting -
IRCCS Maugeri Veruno
Veruno, Italy Not yet recruiting
Study contacts
- Principal investigator: Petronilla Battista, PhD — Istituti Clinici Scientifici Maugeri IRCCS
- Study coordinator: Petronilla Battista, PhD
- Email: petronilla.battista@icsmaugeri.it
- Phone: +39 0807814331
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.