Skip to main content
Clinical Trials/NL-OMON46000
NL-OMON46000CompletedNot Applicable

PRediction Of Cognitive Recovery After Stroke: a role for new MRI modalities in daily clinical practice? - PROCRAS

Sint Elisabeth Ziekenhuis0 sites350 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
350

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Observational

Eligibility Criteria

Ages
18 to 99 (—)

Inclusion Criteria

  • •For cognitive impaired group:
  • •Ischemic stroke (clinical diagnosis, CT-scan confirmed or not)
  • •Age 50 years or older
  • •Montreal Cognitive Assessment (MoCa) score <26 ;For control group
  • •Ischemic stroke (clinical diagnosis, CT-scan confirmed or not)
  • •Age 50 years or older
  • •Montreal Cognitive Assessment (MoCa) score equal to or above 26

Exclusion Criteria

  • •-Pre-existent dementia (clinical diagnosis) and/or Pre-existing cognitive impairment (score of 3.6 or higher on the Informant Questionnaire on Cognitive Decline in the Elderly (IQCODE))
  • •-Life expectancy < 1 year
  • •-Very severe stroke needing long term nursing care facilities
  • •-History of major neurological disease interfering with cognitive functioning
  • •-Pre-stroke dependence in activities of daily living (Barthel Index below 18);
  • •-Insufficient command of the Dutch language in order to participate and understand questionnaires
  • •- Impossibilitiy to participate in a neuropsychological assessment
  • •- Not able to undergo an MRI-scan due to contra-indications

Investigators

Sponsor
Sint Elisabeth Ziekenhuis

Similar Trials