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Study of Stroke & factors that affect outcome

Not Applicable
Conditions
Health Condition 1: I619- Nontraumatic intracerebral hemorrhage, unspecifiedHealth Condition 2: I688- Other cerebrovascular disorders indiseases classified elsewhere
Registration Number
CTRI/2023/07/054778
Lead Sponsor
Hamilton Health Sciences Population Health Research Institute
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Ischemic stroke or ICH

2. 18 years or older

3. Within 16 weeks of the index event

4. ‘Probable stroke’ (high clinical suspicion of stroke based on acute focal neurological deficits in fitting with a neurovascular territory lasting for more than 24 hours, but without imaging confirmation of stroke) OR ‘definite stroke’ (brain imaging confirmed stroke [CT or MRI]).

Exclusion Criteria

1.Patients will be excluded if they are deemed by the investigators to be unlikely to adhere to study processes.

2.If they have a neurological condition (besides stroke) that is associated with cognitive or functional decline

3.An established diagnosis of pre-stroke dementia.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Cognition <br/ ><br>MOCA/t-MOCA <br/ ><br>Oxford Cognitive Screen <br/ ><br>Number symbol coding task <br/ ><br>Function <br/ ><br>SAGE <br/ ><br>smRSq <br/ ><br>Timepoint: 6 months
Secondary Outcome Measures
NameTimeMethod
QoL <br/ ><br>Mortality <br/ ><br>Recurrent stroke or MACE <br/ ><br>New diagnosis of dementia <br/ ><br>Other adverse events (falls/fractures, infections, cancer, seizures) <br/ ><br>Aphasia, fatigue, depression, anxiety, apathy <br/ ><br>Physical activity <br/ ><br>Other (Social Support & Food intake) <br/ ><br>Timepoint: At 6-month
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