PROspective Study to OPTimize thE HEALTH of Patients With TIAs (Transient Ischemic Attacks) and Stroke Admitted to the Hamad General Hospital (PROMOTE-HEALTH)
Stroke, Transient Ischemic Attack (TIA)

About this trial
This is an interventional prevention trial for Stroke focused on measuring cerebrovascular disease, patient management, stroke management, prognosis, 3D Carotid Doppler Imaging, Randomization
Eligibility Criteria
Inclusion Criteria:
- ISCHEMIC STROKE OR TIA including ocular stroke such as Amaurosis Fugax, within the past year (not intracranial hemorrhage or due to trauma, malignancy or cardio-embolic related to structural heart disease)
MEETS AT LEAST ONE OF THE FOLLOWING THREE CRITERIA:
- systolic Bp>140 mmHg but <200 mmHg (at 24 HR from admission/if clinic visit 3 readings 5 minutes apart)
- fasting LDL cholestrol >2.0 (MEASURED WITHIN PREVIOUS 6 MONTH)
- total: HDL cholestrol ratio >4.0 (measured within previous 6 month)
- Willing to participate (by signing consent form)and willing to return for study-related scheduled follow up visits for one year from the time of enrollment into the study
Exclusion Criteria:
- Participation in concurrent interventional trial related to stroke or vascular disease
- Any condition, including foreshortened life-expectancy or severe comorbidities that would preclude treatment benefit or 12-month follow up.
- Institutionalized in a long term care facility
Already on maximal therapy for risk factors:
- On 3 ANTI HTN drugs at maximal dose (if htn is inclusion criteria)
- On maximal dose of statin (if elevated LDL-cholesterol is inclusion criteria)
- CT or MRI shows evidence of primary intracranial hemorrhage or neoplasm
- Active coronary artery disease
- Severe Renal on hemo-dialysis(HD) or Severe Hepatic dysfunction
- Cognitive dysfunction severe enough to interfere with patients ability to give informed consent
- Severe systemic illness that will not allow for the patient to complete the one year trial
- History of intolerance to statins or commonly used anti-hypertensive medications(intolerance/contraindication to statin(if elevated LDL-c is the inclusion criteria)
- Unable to tolerate antiplatelet agents
- Decline of consent
- Reside outside Qatar
- Unable to participate (due cognition, mobility, language barrier)
Sites / Locations
- Hamad Medical CorporationRecruiting
Arms of the Study
Arm 1
Arm 2
No Intervention
Active Comparator
Control; standard of care
Intervention; Lifestyle counselling: Behavioural
All the subjects enrolled in this arm will receive counseling as the usual standard of care by the stroke neurologists. These will include procedures and guidelines as approved by American Heart Association (AHA), follow up and guidance as offered by Hamad General Hospital's policies.
Subjects in this group will receive a more detailed guidance on rigorous management of stroke and will be provided assistance from a stroke trained nurse and pharmacist additional to the counseling offered by the Stroke Neurologist.