F06.7 F06.8 F06.9
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Subjects have cognitive deficits (diagnosis of F06.7 - F06.9, or professional assessment by a clinical neuropsychologist) as a result of a diagnosed acquired brain injury (e.g. stroke). - Subjects have access to a computer with internet connection (PC or laptop; MAC) - Test persons are able to operate the PC and training software independently. - Test persons have sufficient motivation to train cognitive performance with RehaComOnline. - Test persons are continuously available for training during the intervention period.
Exclusion criteria
Exclusion criteria: - a one-time damaging event (e.g. stroke, craniocerebral trauma) occurred more than 2 years ago - Psychological or cognitive limitations that prevent independent training (e.g. severe neglect, aphasic symptoms) - parallel provision of cognitive therapy as part of neuropsychological, psychotherapeutic or occupational therapy treatment - Pregnancy or breastfeeding
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. improvement of health status measured with neuropsychological test: 1.1 Information processing & visual exploration domain. - Test battery for attention assessment (TAP): Alertness, Go/NoGo, divided attention, visual scanning. - Wechsler Adult intelligence, 3rd edition (WAIS-III) : symbol-digit test 1.2. Memory & Executive Functions - Wechsler Memory Scale, revised (WMS-R) spatial span backwards - Regensburg Word Fluency Test (RWT): semantic and phonematic word fluency - Performance Test System (LPS): subtest 3 2. improvement of quality of life and limitations in everyday life (well-being, satisfaction and participation) measured with questionaires - Short scale for measurement of life satisfaction (L-1) - The Hamburg modules for assessing general aspects of psychosocial health for therapeutic practice (HEALTH 49) Modules B,D,E - BESS scale - Scale for assessing satisfaction with cognitive performance Time of assessment: T0 - measures of 1. and 2. for both arms before the intervention T1 - measures of 1. and 2. for both arms directly after the intervention (4-5 weeks after T0) T2 - measures of 2. only for the controll group after finishing the intervention (8-9 weeks after T0) | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Questions for health competence and patient sovereignty 2. Adherence to training (proportion of finished trainings compared to the prescribed trainings) Time of assessment: T0 - for both arms before the intervention T1 - for both arms directly after the intervention (4-5 weeks after T0) T2 - only for the control group after finishing the intervention (8-9 weeks after T0) | — |
Countries
Germany
Contacts
Tagesklinik für kognitive Neurologie