Actively Recruiting
COMPuter-assisted Self-training to Improve EXecutive Function
Led by Bispebjerg Hospital · Updated on 2025-02-20
307
Participants Needed
2
Research Sites
317 weeks
Total Duration
On this page
Sponsors
B
Bispebjerg Hospital
Lead Sponsor
R
Rigshospitalet, Denmark
Collaborating Sponsor
AI-Summary
What this Trial Is About
This project explores the effects of specialized computer-based cognitive rehabilitation (CBCR) targeting executive functions in three groups of patients: Stroke, Cardiac Arrest and Parkinson's Disease. The effect of specialized CBCR is compared to generally cognitively stimulating activities on a computer
CONDITIONS
Official Title
COMPuter-assisted Self-training to Improve EXecutive Function
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of stroke, cardiac arrest, or Parkinson's disease
- Age 18 years or older
- Impaired working memory with CABPad test score of 5 symbols or less backwards
- Access to computer and internet at home
- Able to provide informed consent
- For stroke: within 6 months post-stroke, confirmed by clinical findings and imaging, initial stroke severity NIHSS 3 or higher
- For cardiac arrest: within 6 months post ictus
- For Parkinson's disease: clinical diagnosis and receiving anti-parkinsonian medication
You will not qualify if you...
- Informed consent not provided
- Other neurological or psychiatric diseases expected to affect participation
- Unable to participate as judged by investigator
- For stroke: massive anosognosia for executive dysfunction or denial of executive symptoms, severe aphasia affecting test validity
- For Parkinson's disease: diagnosis of Parkinson's disease dementia according to MDS criteria
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Bispebjerg Hospital
Copenhagen, Denmark
Actively Recruiting
2
Rigshospitalet
Copenhagen, Denmark
Actively Recruiting
Research Team
H
Hanne Christensen, Professor
CONTACT
K
Katrine Sværke, M.Sc. Psych.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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