None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Who agrees to participate in this study and signs a written agreement 2) Adult aged 55 to under 80 3) Who complains of subjective cognitive decline
Exclusion criteria
Exclusion criteria: 1) Who is suspected of having dementia as a result of a neuropsychological examination 2) Who is diagnosed with any axis 1 psychiatric disorders 3) Who has suicidal ideation 4) Who has resistant Hypertension, uncontrolled diabetes, malignancy, severe cerebrovascular disease, heart disease, neuropsychological disease, traumatic brain damage accompanied by loss of consciousness or convulsions, acute stroke, severe hearing and vision impairment 5) Who has taken medications and health functional foods that may affect cognitive and memory function 6) Any contraindications to MRI 7) Participants in other clinical studies 8) Who has hypersensitivity to ingredients contained in the experimental and placebo foods or has experienced severe food allergy reactions 9) Who is deemed inappropriate by investigators to participate in this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cambridge Neuropsychological Test Automated Battery | — |
Secondary
| Measure | Time frame |
|---|---|
| Neuropsychological test and cognitive functional questionnaire;Brain imaging;Safety-related indicators (vital signs, clinical pathological testing, adverse event) | — |
Countries
Korea, Republic of
Contacts
Ewha Womans University