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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03558308
Other study ID # H-18006890
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 1, 2018
Est. completion date July 1, 2021

Study information

Verified date July 2021
Source Bispebjerg Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


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.


Recruitment information / eligibility

Status Completed
Enrollment 72
Est. completion date July 1, 2021
Est. primary completion date January 1, 2021
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility 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

Study Design


Intervention

Behavioral:
Computer 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.
Other:
Sham computerized gaming
Sham training with generally stimulating computer-games

Locations

Country Name City State
Denmark Center for Hjerneskade Amager København

Sponsors (2)

Lead Sponsor Collaborator
Katrine Sværke University of Copenhagen

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary PASAT Paced auditory serial addition test, test of verbal working memory 3 seconds
Primary Trail making test A+B Trail test A: Test of visual attention, trail test B: Test of visual working memory and cognitive shifts 5 minutes
Secondary SDMT Symbol digit modalities test: Test of processing speed 90 seconds
Secondary Word fluency test Test of verbal fluency 1 min
Secondary Digit span (WAIS-IV) Test of verbal memory (forward) and working memory (backward) 5 minutes
Secondary Spatial span (WMS-III) Test of visuospatial memory (forward) and visuospatial working memory (backward) 5 minutes
Secondary Stroop colour and word test Test of inhibition 3 minutes
Secondary BNI-FS Barrow Neurological Institute Fatigue Scale: Test of fatigue after brain injury 10 minutes
Secondary Quality of Life after Brain Injury (QOLIBRI) Questionnaire about quality of life 10 minutes
Secondary Wordlist, Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) Verbal memory test 10 minutes
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