Cross-sectional characterisation of elderly using the NeuroCart.
- Conditions
- Alzheimer's diseasedementia10029299
- Registration Number
- NL-OMON43551
- Lead Sponsor
- Centre for Human Drug Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Withdrawn
- Sex
- Not specified
- Target Recruitment
- 1000
1. Males and females, aged 60 and older (inclusive);
2. Willing and able to perform the cognitive tests, as evidenced by performance on the training session of the cognitive tests.
3. Willing and able to give written informed consent and to comply with the study procedures.
1. Legal incapacity or inability to understand or comply with the requirements of the study;
2. Evidence of severe cognitive deterioration, as indicated by a diagnosis of severe cognitive disorder (including but not limited to Alzheimer*s disease, Lewy Body Dementia, Fronto-temporal Dementia);
3. History or symptoms of significant psychiatric disease (including but not limited to clinical depression, schizophrenia);
4. A Mini Mental State Examination (MMSE) score of < 18;
5. A Geriatric Depression Scale (GDS) score of *6;
6. Presence of drug abuse, or positive urine drug screen (UDS) at screening or occasion;
7. Presence of severe alcohol abuse (daily alcohol consumption exceeding 2 standard drinks per day on average for females or exceeding 3 standard drinks per day on average for males (1 standard drink = 10 grams of alcohol)), or a positive breath alcohol test at screening or occasion;
8. Any other reason that it is not safe or ethical to allow a subject to participate in the study in the opinion of the investigator.
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method