Skip to content

Computer based cognitive flexibility training after stroke

Computer based cognitive flexibility training after stroke - TAPASS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON40530
Enrollment
160
Registered
2013-07-09
Start date
2013-09-17
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

cerebrovascular accident Stroke

Interventions

Participants will be randomized over three conditions: online cognitive flexibility training, online mock training (active control), or waiting list. The training duration is 12 weeks during which p

Sponsors

Vrije Universiteit Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1) Suffered from stroke and referred to rehabilitation; 2) Presence of cognitive dysfunction due to stroke; 3) Age between 30 and 80 years; 4) Daily access to computer with internet connection and able to use mouse; 5) lnformed consent for study participation.

Exclusion criteria

Exclusion criteria: 1) Any disease other than stroke which results in severe cognitive impairments 2) Severe psychological, psychiatric, or somatic comorbidity which could strongly influence the performance on the neuropsychological assessment and training possibilities 3) Mentally (Telephone Interview Cognitive Status (TICS) score

Design outcomes

Primary

MeasureTime frame
The primary outcome is executive functioning as measured by several neuropsychological tasks (Fluency, Tower of London, Trail Making Test, letter-number sequencing) See protocol for a description of these tasks.

Secondary

MeasureTime frame
1) Cognitive flexibility as measured by switchcost (reactietimes op switchtrials compared to reaction times on non -switchtrials) on the switch task. 2) Cognitive functioning as measured by several neuropsychological tasks and computer tasks (see protocol) 3) Training improvement 4) Subjective cognitive functioning and functioning in daily life as measured by: dysexecutive questionnaire (DEX), Cognitive Failure Questionnaire (CFQ), Utrechtse Schaal voor Evaluatie en Revalidatie- Participatie (USER-P), Instrumental activity of daily life scale (IADL), en Short Form Health Survey (SF-36) 5) Imaging analyses (resting state fMRI, Diffusion Tensor Imaging, Voxel Based Morphometry)

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)