About this trial
Study is Interventional, cross-sectional, clinical trial without drug and without device
Eligibility criteria
Qualifiers
subjective cognitive decline, defined as self-experienced persistent decline in cognitive capacity in comparison with a previously normal status and unrelated to an acute event; normal performance on standardised cognitive tests adjusted for age, sex, and education; decline cannot be explained by psychiatric or other neurologic disease, medical disorder, medication, or substance use; no functional impact on daily life activities
mild cognitive decline, defined as persistent decline in cognitive performance (in comparison with a previous status) reported by the subject or by an informed caregiver; or observed by change on longitudinal cognitive testing; cognitive performance below expected range for that individual based on cognitive test performance (adjusted for age, sex, and education); performs daily life activities independently (but cognitive difficulty may result in detectable but minimal functional impact on the more complex activities of daily life, either self-reported or corroborated by a study partner); Clinical Dementia Rating Scale = 0.5
Ability to sign and understand the informed consent form
Disqualifiers
Age under 50 or over 85 years
Non-native Italian speakers
Non degenerative and secondary forms of dementia
Previous or current participation in clinical trials with anti-amyloid agents
Trial design
Treatments tested in this trial
- Neuropsychological Assessments and Other Questionnaires
- Blood Exams, Fluid Biomarkers, Genetics
- Connectivity Analysis
- Physical Activity
- Healthentia
- Eligence
- Nutrition