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Subjective Cognitive Impairment Cohort, a focus on the earliest changes leading to Alzheimer*s disease.

Recruiting
Conditions
Preclinical Alzheimer's disease
first symptoms of Alzheimer's disease
10012272
Registration Number
NL-OMON53088
Lead Sponsor
Amsterdam University Medical Center, VU Universty Medical Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
500
Inclusion Criteria

- Label of subjective memory complaints (i.e. no diagnosis of dementia, mild
cognitive impairment, psychiatric or neurological disorder explaining cognitive
complaints).
- Signed informed consent projects P2005_160, P2000_211, P2016_061 or P2016_409.
- Age * 45 year.

Exclusion Criteria

- Insufficient knowledge of Dutch language.
- Major psychiatric disorder, such as psychosis, schizophrenia, severe
personality disorder or depression with vital signs, abuse of alcohol or other
substances.
- Neurological disorder such as Parkinson*s disease, symptomatic stroke, mental
retardation.
- Acquired Immune Deficiency Syndrome (AIDS) or Human Immunodeficiency Virus
(HIV).

Study & Design

Study Type
Observational invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Clinical progression, i.e. progression to a clinical diagnosis of MCI or<br /><br>dementia. </p><br>
Secondary Outcome Measures
NameTimeMethod
<p>- Decline in cognitive functioning on neuropsychological testing (i.e. memory,<br /><br>language, visuospatial functioning, attention, executive functioning etc).<br /><br>- Decline in daily functioning as measured using the Amsterdam IADL<br /><br>questionnaire<br /><br>- Amyloid-positivity (as measured using CSF biomarkers and/or amyloid-PET) as<br /><br>an endophenotype for AD. </p><br>
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