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CBCR for Executive Functions in Patients With ABI in the Chronic Phase

The Effects of Computer Based Cognitive Rehabilitation on Executive Functions in Patients With Acquired Brain Injury in the Chronic Phase: A Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03558308
Enrollment
72
Registered
2018-06-15
Start date
2018-08-01
Completion date
2021-07-01
Last updated
2021-07-22

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

Conditions

Acquired Brain Injury, Cognitive Symptom, Executive Dysfunction

Brief summary

This study examines the effects of computerbased cognitive rehabilitation on executive functions in the chronic phase after acquired brain injury

Detailed description

This study examines the effects of computerbased cognitive rehabilitation on executive functions in the chronic phase after acquired brain injury using two clinically developed programmes and one sham-intervention. Furthermore, the study consists of Groups that receives the computerized training both with and witouth support from a professional.

Interventions

OTHERSham computerized gaming

Sham training with generally stimulating computer-games

BEHAVIORALComputer based cognitive rehabilitation

Computer based cognitive rehabilitation is a supplementary computerized tool for cognitive rehabilitation design to train various cognitive functions. Many programmes are available. The current study investigates the effects on two such programmes on rehabilitation of executive functions in the chronic phase after acquired brain injury.

Sponsors

University of Copenhagen
CollaboratorOTHER
Katrine Sværke
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

Patients know that one of the conditions is a control-condition not expected to have significant clinical effects (required by the danish scientific committee), but they don't know which treatment condition they are randomised to. The outcome assessor is blind to the group allocation of patients.

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Persons who are able to give an informed consent both verbally and in writing * Persons in the chronic phase after stroke or traumatic brain injury (more than one year post onset) * Persons who score less than the 30. Percentile in one or more of the primary outcome measures outlined above.

Exclusion criteria

* Persons with neurodegenerative diseases * Persons with diseases which can influence executive functions such as ADHD * Persons who are motorically or cognitively unable to use a tablet and complete the CBCR-training

Design outcomes

Primary

MeasureTime frameDescription
PASAT3 secondsPaced auditory serial addition test, test of verbal working memory
Trail making test A+B5 minutesTrail test A: Test of visual attention, trail test B: Test of visual working memory and cognitive shifts

Secondary

MeasureTime frameDescription
Digit span (WAIS-IV)5 minutesTest of verbal memory (forward) and working memory (backward)
Spatial span (WMS-III)5 minutesTest of visuospatial memory (forward) and visuospatial working memory (backward)
Stroop colour and word test3 minutesTest of inhibition
SDMT90 secondsSymbol digit modalities test: Test of processing speed
Quality of Life after Brain Injury (QOLIBRI)10 minutesQuestionnaire about quality of life
Wordlist, Repeatable Battery for the Assessment of Neuropsychological Status (RBANS)10 minutesVerbal memory test
BNI-FS10 minutesBarrow Neurological Institute Fatigue Scale: Test of fatigue after brain injury
Word fluency test1 minTest of verbal fluency

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026