Actively Recruiting
FIND Stroke Recovery - A Longitudinal Study
Led by Göteborg University · Updated on 2025-04-02
600
Participants Needed
1
Research Sites
673 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Stroke survivors frequently suffer disabilities including motor and cognitive problems, impairments in speech and vision, depression, and several other disabilities that worsen their quality of life. Some will recover fully after stroke and others will have permanent impairments. Few studies show trajectories of recovery in different domains after stroke, hence recovery time-lines are not fully known. Also, the whole range of mechanisms leading to recovery are not precisely known (1). To monitor those mechanisms one can utilize biomarkers. In parallel to the studies of recovery, studies on time series of biomarkers after stroke are limited (2). Hence, a crucial first step to increase knowledge on biomarkers of stroke recovery is to gain a better understanding of the time course of both stroke recovery and biomarker patterns. Biomarkers can later be used for outcome predictions after stroke.
CONDITIONS
Official Title
FIND Stroke Recovery - A Longitudinal Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- First-ever acute ischemic stroke or intracerebral hemorrhage
- Admitted to the stroke units at Sahlgrenska University Hospital in Gothenburg, Sweden
- Able to provide informed consent or have next-of-kin provide consent
You will not qualify if you...
- Pre-stroke modified Rankin Scale score of 3 or higher
- Severe neurodegenerative disease, brain tumor, or terminal illness
- Unlikely to understand or comply with study procedures during follow-up visits
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Department of Neurology, Department of Neurorehabilitation and Department of Clinical Genetics, Sahlgrenska University Hospital
Gothenburg, Sweden, SE-41345
Actively Recruiting
Research Team
C
Christina Jern, MD, PhD
CONTACT
J
Jood Katarina, MD, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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