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NCT04229056Active, not recruiting

COMPuter-assisted Self-training to Improve EXecutive Function

Computer-Assisted Self-Training to Improve Executive Function Versus Unspecific Training in Patients After Stroke, Cardiac Arrest or in Parkinson's Disease: A Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 2 Oct 2026

Brief summary (registry, in English)

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

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
307 (estimated)
First submitted
3 Jan 2020
Start date
1 Jun 2020
Primary completion date
5 Nov 2026
Lead sponsor
Bispebjerg Hospital
NCT number
NCT04229056

What you commit to

  • Study type: Interventional
  • Planned participants: 307
  • From 1 Jun 2020 to the primary completion date, 5 Nov 2026
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Other neurological or psychiatric disease which is expected to influence the patient's ability to participate in the trial according to the investigator
  • Diagnosis of PD Dementia according to the MDS PD Dementia criteria

Other

  • Informed consent not provided
  • Not able to participate according to investigator
  • Patients with massive anosognosia for executive dysfunction or patients with no subjective feeling of executive dysfunction (Patient sustains total denial of executive symptoms over time)
  • Patients with severe aphasia, in which it is unclear whether the patient's performance on a neuropsychological test-battery is due to aphasia and not executive dysfunction.

Who the study is looking for

  • A diagnose of stroke, cardiac arrest or Parkinson's disease.
  • Aged 18 years or older.
  • Impaired working memory measured with CABPad working memory test, cut off for inclusion: 5 symbols or less backwards
  • Computer and internet access at home.
  • Providing informed consent.
  • Inclusion within 6 months post-stroke
  • Stroke confirmed by clinical findings and imaging, both AIS and ICH is allowed.
  • Initial stroke severity \>/= NIHSS 3.
  • Inclusion within 6 months post ictus.
  • Clinical diagnosis of PD.
  • Anti-parkinsonian medical treatment (dopaminergic or other).

Age in the registry: 18 years to 100 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Bispebjerg Hospital
Coordinator of this site? Confirm its status
CopenhagenDenmarkUnknown status
Rigshospitalet
Coordinator of this site? Confirm its status
CopenhagenDenmarkUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.