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

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON53088
Enrollment
5
Registered
2013-12-09
Start date
2014-06-02
Completion date
Unknown
Last updated
2025-11-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Preclinical Alzheimers disease

Interventions

None listed

Sponsors

Amsterdam UMC
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

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

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).

Design outcomes

Primary

MeasureTime frame
Clinical progression, i.e. progression to a clinical diagnosis of MCI or dementia.

Secondary

MeasureTime frame
- Decline in cognitive functioning on neuropsychological testing (i.e. memory, language, visuospatial functioning, attention, executive functioning etc). - Decline in daily functioning as measured using the Amsterdam IADL questionnaire - Amyloid-positivity (as measured using CSF biomarkers and/or amyloid-PET) as an endophenotype for AD.

Countries

Netherlands

Contacts

Public ContactA.C. van Harten

Amsterdam UMC

a.vanharten@amsterdamumc.nl0204448548

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)