Prediction Of Cognitive Recovery After Stroke (PROCRAS)
PROCRAS was a longitudinal, prospective study conducted at the Elisabeth-Tweesteden Hospital, Tilburg, in the Netherlands. The study included patients 50 years of age and older, admitted with a clinical diagnosis of acute ischemic stroke and evidence of a cognitive disorder during hospitalization. Between July 1, 2016, and May 10, 2018, 217 people agreed to participate in the PROCRAS study. The primary endpoint is the recovery of cognitive function one year after stroke in patients with a confirmed post-stroke cognitive disorder. The secondary endpoint is deterioration of cognitive function in the first year after stroke.
Study design
Cohort - clinical
Number of participants at first data collection
217 (participants)
Age at first data collection
≥ 50 years (participants)
Participant year of birth
Varied (participants)
Participant sex
All
Representative sample at baseline?
No
Sample features
Country
Year of first data collection
2016
Primary Institutions
Elisabeth-Tweesteden Hospital
Profile paper DOI
Funders
The Netherlands Organisation for Health Research and Development (ZonMW)
Ongoing?
No
Data types collected
- Computer, paper or task testing (e.g. cognitive testing, theory of mind doll task, attention computer tasks)
- Interview – face-to-face
- Interview – phone
- Self-completed questionnaire – unspecified
- None
- Diffusion Tensor Imaging (DTI)
- Magnetic Resonance Imaging (MRI)
- None
Engagement
Keywords
Consortia and dataset groups
