F00 F01 F02 F03 F04 F06.7
Conditions
Interventions
Group 1: Patients at the ophtalmology clinics that undergo routine OCT-assessment will be asked for participation in the study. Upon giving written informed consent they will undergo a semi-structured
Sponsors
Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE)
Eligibility
Sex/Gender
All
Age
65 Years to No maximum
Inclusion criteria
Inclusion criteria: Routine OCT-assessment during routine visit at the ophtalmologist, sufficient language skills
Exclusion criteria
Exclusion criteria: Glaucoma, advanced cataract, diabetic retinopathy/ Makulopathy, Assessment not applicable (according to the treating physician)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| How big is the proportion of people with cognitive impairments identified during routine OCT-assessment? | — |
Secondary
| Measure | Time frame |
|---|---|
| How many patients participate in a cognitive screening? How many people do show cognitive impairment and lower thickness of the retina? How many people do have a cognitive impairment, a thinner retina AND a formal diagnosis of dementia? How many people get a guideline-oriented diagnostic of cognitive impairment afterwards? What other factors are associated with the biomarker, the cognitive status and the formal diagnosis of dementia? | — |
Countries
Germany
Contacts
Public ContactGreta Otto
Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE)
Outcome results
None listed