Study of Stroke & factors that affect outcome
- 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
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]).
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
Name Time Method 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
Name Time Method 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