Testing the equivalence/non-inferiority of the digital versus the paper-based measurement method of cognitive impairments
Not Applicable
Recruiting
- Conditions
- U51
- Registration Number
- DRKS00019114
- Lead Sponsor
- Charité - Universitätsmedizin BerlinForschungsgruppe Geriatrie
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 245
Inclusion Criteria
Arm 1 (inpatient geriatric patients): Age = 65 years, presence of patient information and signed informed consent.
Arm 2 (healthy seniors): Age = 65 years, capacity for consent, presence of subject information and signed informed consent.
Exclusion Criteria
Arm 1 (inpatient geriatric patients): legal representative.
Arm 2 (healthy seniors): severe cognitive disorders, psychiatric disorders, severe auditory, visual, linguistic, sensory or motoric impairments, severe systemic diseases, mild or severe pain, CNS diseases and diseases affecting the CNS, cerebrovascular disease, current study participation.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Arm 1: Mini-Mental Status Test (inpatient geriatric patients) <br>Arm 2: Trail Making Test A/B, Clock-Drawing Test, Rey Osterrieth Complex Figure Test (healthy seniors)
- Secondary Outcome Measures
Name Time Method Arm 1: Extended Barthel-Index, Depression in the Elderly Scale, Geriatric Depression Scale (inpatient geriatric patients)<br><br>Arm 2: none (healthy seniors)<br>