Stroke Cancer
Conditions
Interventions
The study will involve a short questionnaire (about 30 minutes) through an interview with the local study team, where they will collect information on participants' past medical history, lifestyle-rel
Sponsors
University of Oxford
Eligibility
Sex/Gender
All
Age
18 Years to 54 Years
Inclusion criteria
Inclusion criteria: 1. Patient is willing and able to give informed consent for participation in the study, or favourable consultee advice for adults lacking capacity OR If consent or consultee advice was not feasible, CAG/Section 251 support for data collection 2. Male or Female, aged 18 to 54 years 3. A diagnosis of ischaemic stroke (including retinal artery occlusion) OR A diagnosis of intracerebral haemorrhage
Exclusion criteria
Exclusion criteria: 1. Intracerebral haemorrhage as a result of trauma 2. Ischaemic stroke or intracerebral haemorrhage as a result of cerebral venous thrombosis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Traditional vascular risk factors (e.g. hypertension, diabetes, hyperlipidaemia, obesity, smoking, alcohol excess) measured using questionnaire/medical records at baseline 2. Emerging risk factors (e.g. depression, anxiety and other mental health conditions, long working hours, stress, autoimmune conditions, oral health) measured using questionnaire/medical records at baseline | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Long-term vascular (recurrent stroke, myocardial infarction, dementia and vascular death) and non-vascular outcomes (cancer and mental health conditions) measured using medical record linkage at 5, 10, 20 and 30 years 2. Stroke severity measured using National Institutes of Health Stroke Scale (NIHSS) at baseline 3. Disability measured using modified Rankin scale at baseline in the first instance 4. Quality of life measured using EQ-5D at baseline in the first instance | — |
Countries
England, United Kingdom
Contacts
Public ContactLinxin Li
Outcome results
None listed