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Post-stroke Cognitive Impairment — CogStroke  

Cognitive Performance Clinical Trial

Official title:
Prediction of Post-stroke Cognitive Decline and Dementia: Impact of Cognitive Reserve and Post-stroke Life Style

Clinical Trial Summary

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

Clinical Trial 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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05653141
Study type Observational
Source University Hospital Inselspital, Berne
Contact Roza M. Umarova, PD Dr.
Phone +41316327000
Email roza.umarova@insel.ch
Status Recruiting
Phase
Start date December 17, 2020
Completion date October 31, 2026
View Details
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