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Forecasting outcomes in cognition after stroke using strategic lesion sites - Predicting cognitive impairment following ischemic stroke

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON58203
Enrollment
50
Registered
2025-05-22
Start date
2026-03-06
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Stroke, ischemic stroke, brain infarct, cerebrovascular accident, CVA, cerebral infarction Stroke

Interventions

NA.

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Clinical diagnosis of acute ischemic stroke (first-ever or recurrent) admitted to the hospital within 1 week of symptom onset Age =18 yearsPresence of acute neurological deficit lasting more than 24 hoursDischarge destination directly home (with or without outpatient rehabilitation)Able to undergo brain-MRI within 1 week after stroke onset

Exclusion criteria

Exclusion criteria: At baseline:Pre-stroke dementia (known diagnosis of dementia or Informant Questionnaire on Cognitive Decline in the Elderly (IQCODE) >3.6Psychiatric or neurological disease other than the qualifying event with an active interference on cognition, as judged by a clinician Insufficient command of the Dutch language to undergo neuropsychological assessmentContra-indications to MRI (e.g., non-compatible pacemaker or implants, severe claustrophobia, cardiopulmonary disease)Condition interfering with participation in neuropsychological assessment (e.g., severe aphasia interfering with comprehension of test-instructions) Additional exclusion criteria based on MRI:No acute infarct visibleAlternative diagnosis for acute symptoms identified on imaging (e.g., brain tumor)

Design outcomes

Primary

MeasureTime frame
Presence or absence of PSCI based on multidomain neuropsychological assessment at 6 months. 

Secondary

MeasureTime frame
Patient reported outcome measures (PROMs) on ability to- and satisfaction with participation in social roles and activities

Countries

Netherlands

Contacts

Public ContactC. Didderen

Universitair Medisch Centrum Utrecht

policvz@umcutrecht.nl088 75 579 89

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Jun 11, 2026