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Clinical Trials/NL-OMON43551
NL-OMON43551
Withdrawn
Not Applicable

Cross-sectional characterisation of elderly using the NeuroCart. - Cross-sectional NeuroCart study in elderly.

Centre for Human Drug Research0 sites1,000 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Alzheimer's disease
Sponsor
Centre for Human Drug Research
Enrollment
1000
Status
Withdrawn
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational invasive

Investigators

Eligibility Criteria

Inclusion Criteria

  • 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.

Exclusion Criteria

  • 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.

Outcomes

Primary Outcomes

Not specified

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