Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Cheng Sheng Chen
Age
50–85
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
For MCI/dementia groups:
1. Patient diagnosed with MCI, AD dementia, VaD or DLB
2. Participant who is 50-85 years of age
3. Taiwanese who had finished primary education
4. Participant (or legally acceptable representative) who signed the written ICF
1. Healthy volunteers without objective cognitive impairment
2. Participant who is 50-85 years of age
3. Taiwanese who had finished primary education
4. Participant who signed the written ICF
You may not be if
1. Participant with GDS score ≥ 10
2. Participant with CDR score \> 1 (Assessment result within 6 months can be used conditionally.)
3. Participant with MMSE score ≤ 17 (MMSE score will be converted from CASI score. Assessment result within 6 months can be used conditionally.)
4. Participant diagnosed with Schizophrenia
5. Participant diagnosed with Parkinson's disease
6. Participant diagnosed with cancer (except basal cell skin carcinoma) in the past two years
7. Participant diagnosed with uncontrolled diabetes
8. Participant with regular alcohol use exceeding two standard drinks per day for women or four per day for men (one standard drink corresponds to 350 cc of beer)
9. Participant unable to take CBB test according to the investigator's discretion, such as blindness
10. Participant who, in the opinion of the investigator or medical monitor, should not participate in the study
For HC group:
1. Participant with GDS score ≥ 10
2. Participant diagnosed with Schizophrenia
3. Participant diagnosed with Parkinson's disease
4. Participant diagnosed with cancer (except basal cell skin carcinoma) in the past two years
5. Participant diagnosed with uncontrolled diabetes
6. Participant with regular alcohol use exceeding two standard drinks per day for women or four per day for men (one standard drink corresponds to 350 cc of beer)
7. Participant unable to take CBB test according to the investigator's discretion, such as blindness
8. Participant who, in the opinion of the investigator or medical monitor, should not participate in the study
