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Evaluation of positive effects of computer-based cognitive therapy in the home context on healthcare supply

Evaluation of positive effects of computer-based cognitive therapy in the home context on healthcare supply - Home_CT

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
DRKS
Registry ID
DRKS00026651
Enrollment
48
Registered
2022-01-17
Start date
2021-10-05
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

F06.7 F06.8 F06.9

Interventions

Group 1: 4-5 weeks of individually adapted computer-based cognitive training with RehaComOnline at home without additional therapeutic care Group 2: Waiting list control group with training starting a

Sponsors

HASOMED GmbH
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

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

MeasureTime 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

MeasureTime 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

Public ContactJuliane Weicker

Tagesklinik für kognitive Neurologie

Juliane.Weicker@medizin.uni-leipzig.de0341 9724991

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026