STroke imAging Prevention and Treatment (START): PrePARE Prediction and Prevention to Achieve optimal Recovery Endpoints after stroke
- Conditions
- StrokeDepressionCognitionStroke - IschaemicPhysical Medicine / Rehabilitation - Occupational therapyMental Health - Depression
- Registration Number
- ACTRN12610000987066
- Lead Sponsor
- ational Stroke Research Institute (NSRI)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 100
1. Patients presenting with ischaemic stroke.
2. Patient, family member or legally responsible person depending on local ethics requirements has given informed consent for participation in the START_PrePARE study
3. Patient’s age is > 18 years.
1. Patients who are non-English speaking
2. Contraindication to MR imaging on 3Tesla scanner.
3. Pre-stroke MRS score of greater or equal to 2 (indicating previous disability)
4. Any terminal illness such that the patient would not be expected to survive more than 1 year.
5. Pregnant women (clinically evident)
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Functional and structural changes in the brain: i.e cortical thickness, fibre tract connection and functional resting-state connections.[3 and 12 months];Depression (Montgomery-Asberg Depression Rating Scale with non-verbal supports)[3 and 12 months];Functional status: Functional Independence (mRS), Cognition (MoCA, MMSE, Trails-B, Digit span, Shape Cancellation Task, RCPM, Stroop test), and Sensorimotor (Action Research Arm Test, Tactile Discrimination Test, Timed up and go test)[3 and 12 months]
- Secondary Outcome Measures
Name Time Method Participation (Activity Card Sort)[3 and 12 months];Quality of life (Stroke Impact Scale)[3 and 12 months];Mortality and recurrent stroke[3 and 12 months]