Cologne instrument for the nonverbal assessment of subjective impairments in cognition and activities of daily living (KINO-MCI)
- Conditions
- F06.7Mild cognitive disorder
- Registration Number
- DRKS00033038
- Lead Sponsor
- niklinik Köln
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 380
Control group:
- Vision and hearing: unimpaired or sufficiently corrected (glasses, hearing aid, etc.)
- Sufficient knowledge of German
- Sufficient language skills (documented in the Aphasie-Check-Liste short version)
- Disease status: no known neurological diseases
- Cognitive status: no known impairments
- Consent: consented and signed
Clinical patients:
- Vision and hearing: unimpaired or sufficiently corrected (glasses, hearing aid, etc.)
- Sufficient knowledge of German
- Sufficient language skills (documented in the Aphasie-Check-Liste short version)
- Disease status: patients undergoing inpatient or outpatient treatment at the Clinic and Polyclinic for Neurology
- Cognitive status: patients with subjective cognitive impairment, mild cognitive impairment and mild dementia of various etiologies
- Consent: consented and signed
Control group:
- Vision and hearing: impaired (so that the instructions cannot be conveyed either audibly or visually)
- Limited knowledge of German
- Substantial language impairments (documented in the Aphasie-Check-Liste short version)
- Disease status: known neurological diseases
- Cognitive status: substantial impairments
- Consent: not consented, not signed
Clinical patients:
- Vision and hearing: impaired (so that instructions cannot be conveyed either audibly or visually)
- Limited knowledge of German
- Substantial language impairments (documented in the Aphasie-Check-Liste short version)
- Disease status: patients in whom neurological diseases have been reliably ruled out. Moderate or severe illnesses that interfere with the ability to complete the survey
- Cognitive status: neither subjective nor psychometrically verifiable cognitive impairment, patients with severe dementia (DemTect = 6 points)
- Consent: not consented, not signed
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary objective: The aim of the present study is to apply and validate a newly developed, visually designed, multidimensional screening instrument (Cologne instrument for the nonverbal assessment of subjective impairments in cognition and activities of daily living; KINO-MCI) for the language-reduced assessment of subjectively experienced changes in cognition and ADL-activities in a neurological cohort (including healthy control subjects). In this way, the differential diagnosis of age-associated cognitive changes vs. MCI vs. mild dementia should be improved.
- Secondary Outcome Measures
Name Time Method