Baseline | 12 months | 24 months | 36 months | Assessed by | Source | |
---|---|---|---|---|---|---|
Informed consent | √ | Research assistant | Participant and informant | |||
Demographics | √ | √ | √ | √ | Research assistant | Participant and informant |
MMSE [35] | √ | √ | √ | √ | Physician | Participant |
CDR [34] | √ | √ | √ | √ | Physician | Participant and informant |
Subjective cognitive functioning [17] | √ | √ | √ | √ | Physician | Informant |
Neuropsychological assessment | √ | √ | √ | √ | Psychologist | Participant |
Physical examination & structural medical review | √ | √ | √ | √ | Physician | Participant and informant |
Medications (prescribed & taken) | √ | √ | √ | √ | Physician | Participant and informant |
Hospitalization (if any) | √ | √ | √ | Research assistant | Participant and informant | |
Syndromal diagnoses | √ | √ | √ | √ | Physician | Participant and informant |
Comorbidities (CIRS-G) [18] | √ | √ | √ | √ | Physician | Participant and informant |
√ | √ | √ | √ | Research assistant | Participant and informant | |
DAD (disability assessment) [21] | √ | √ | √ | √ | Research assistant | Informant |
GDS-15 (depression, self-reported) [22] | √ | √ | √ | √ | Research assistant | Participant |
NPI (neuropsychiatric symptoms) [23] | √ | √ | √ | √ | Research assistant | Informant |
Euroqol 5D [24] | √ | √ | √ | √ | Research assistant | Informant |
Care resource use | √ | √ | √ | √ | Research assistant | Informant |
Refusal or withdrawal data | √ | √ | √ | √ | Research assistant | Participant and informant |
Institutionalization (outcome & date) | √ | √ | √ | Research assistant | Participant and informant | |
Death (outcome & date) | √ | √ | √ | Research assistant | Informant |