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Post-stroke Cognitive Impairment (CogStroke)

R

Roza Umarova

Status

Active, not recruiting

Conditions

First-ever Ischemic Stroke
Cognitive Performance

Study type

Observational

Funder types

Other

Identifiers

NCT05653141
Studien-Nr. 4599

Details and patient eligibility

About

Present study aims to track the post-stroke cognitive trajectories and to investigate its inter-individual variability.

Full description

The study aim is to establish a model capturing patients' inter-individual variability in susceptibility to stroke damage to predict stroke-induced cognitive trajectories. This is a prospective longitudinal observational national monocentric study for 6 years (recruitment during the first 3 years). The investigators perform comprehensive neuropsychological testing in i) acute stroke phase (0-10 days post-stroke), ii) sub-acute stroke phase (3 months post-stroke), and iii) chronic stroke phase (12 months and 3 years post-stroke). At each time point, cognitive performances as well as clinical and functional status will be assessed. Furthermore, the investigators will assess the proxies of cognitive reserve and the level of post-stroke physical activity.

Enrollment

335 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ≥18 years old
  • First-ever anterior circulation ischemic stroke confirmed by routine MRI
  • Time of enrollment: ≤ 10 days from stroke onset.

Exclusion criteria

  • Previous stroke anamnestic or based on clinical imaging
  • Additional stroke in posterior circulation
  • Conditions that preclude the cognitive testing (e.g. delirium, intubation, reduced vigilance
  • Neurological or psychiatric conditions that preclude the data interpretation (e.g. pre-stroke dementia, schizophrenia, brain tumor, regular intake of benzodiazepine, depression)
  • MRI contraindication
  • Native language other than German, French or Italian

Trial design

335 participants in 1 patient group

Stroke patients
Description:
Adults with first-ever anterior circulation stroke

Trial contacts and locations

1

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Central trial contact

Laura Gallucci, MSc; Roza M. Umarova, PD Dr.

Data sourced from clinicaltrials.gov

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