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

Primary Purpose

Stroke, Transient Ischemic Attack (TIA)

Status
Unknown status
Phase
Not Applicable
Locations
Qatar
Study Type
Interventional
Intervention
Aggressive Management
Sponsored by
Hamad Medical Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

No Intervention

Active Comparator

Arm Label

Control; standard of care

Intervention; Lifestyle counselling: Behavioural

Arm Description

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.

Outcomes

Primary Outcome Measures

Progression/regression of 3D plaque volume
3D carotid doppler imaging studies

Secondary Outcome Measures

Measurement of blood pressure
management of life style
Measurement of Lipid levels
management of lifestyle

Full Information

First Posted
June 30, 2016
Last Updated
September 5, 2018
Sponsor
Hamad Medical Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT02868723
Brief Title
PROspective Study to OPTimize thE HEALTH of Patients With TIAs (Transient Ischemic Attacks) and Stroke Admitted to the Hamad General Hospital
Acronym
PROMOTE-HEALTH
Official Title
PROspective Study to OPTimize thE HEALTH of Patients With TIAS (Transient Ischemic Attack) and Stroke Admitted to the Hamad General Hospital
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Unknown status
Study Start Date
November 12, 2017 (Actual)
Primary Completion Date
November 30, 2019 (Anticipated)
Study Completion Date
December 30, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hamad Medical Corporation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This will be a prospective randomized 2 year study of patients admitted to the Hamad General Hospital (HGH) and the Stroke Prevention Clinic with a diagnosis of ischemic stroke (IS) and Transit ischemic attacks (TIAs). After signing of the informed consent forms and initial evaluation and investigations, all patients enrolled in the two arms ( study arm and control arm) of the study will be followed for one year (monthly visits for the first three months followed by visits three months until completion of study: total of 6 follow up visits) and the pre-specified investigations repeated at the one year follow up. In one arm (the control group), the patients will be offered best risk factor management strategies as currently being practiced by stroke specialists at HGH in Qatar. And in the second ( the subject group) arm, with assistance of a nurse-practitioner and pharmacist, the investigators will make aggressive attempts to meet "to target" defined risk factors and have the evaluations and investigations completed as in the initial year cohort. All patients will have risk factor stratification according the Framingham Risk Score (FRS) and the change in score measured over time.The primary objective will be to determine if an approach that utilizes a comprehensive strategy results in a significantly outcome. A clinically 'meaningful' difference in the blood pressure (BP) and lipid control of 10% between the aggressively managed versus patients treated with the standard of care will require minimum of 200 patients in each group (alpha error set at 0.05 and beta error at 0.20, power 80%) to be recruited over 1 year and followed for one year (total study duration 2 years). All patients will have screening magnetic resonance imaging (MRI) (including gradient echo (GRE) sequence), carotid 3D Doppler measurement of plaque volume, and PAD assessments, C-reactive protein (CRP) and evaluation for protein urea at baseline. These studies will be repeated in 1 year at the time of exit from the study. The co-primary objective would be to monitor progression (or regression) of plaque build-up on 3D Doppler imaging of the carotid arteries between the two cohorts. The investigators hypothesize that aggressive management of vascular risk factors to "recommended target levels" will lead to better vascular health. Compared to current practice, comprehensive and coordinated approach at preventive measures will lead to more patients with better control of blood pressure and lipid levels. Improved risk factor management will result in slowing of atherosclerosis and its downstream effects which will be measurable on sophisticated blood and imaging testing. Clinically this will translate into fewer hospital re-admissions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Transient Ischemic Attack (TIA)
Keywords
cerebrovascular disease, patient management, stroke management, prognosis, 3D Carotid Doppler Imaging, Randomization

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
400 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control; standard of care
Arm Type
No Intervention
Arm Description
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.
Arm Title
Intervention; Lifestyle counselling: Behavioural
Arm Type
Active Comparator
Arm Description
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.
Intervention Type
Other
Intervention Name(s)
Aggressive Management
Intervention Description
With the aid of the nurse and pharmacist, the individuals in the interventional group will receive additional management of stroke by change is diet plan, increased exercise
Primary Outcome Measure Information:
Title
Progression/regression of 3D plaque volume
Description
3D carotid doppler imaging studies
Time Frame
one year
Secondary Outcome Measure Information:
Title
Measurement of blood pressure
Description
management of life style
Time Frame
one year
Title
Measurement of Lipid levels
Description
management of lifestyle
Time Frame
one year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
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)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
YAHIA Z BASHIER IMAM, MBBS,MD,MRCP,MRCPE
Phone
55246887
Email
yimam@hamad.qa
First Name & Middle Initial & Last Name or Official Title & Degree
NIMA K EL KHAWAD MOHAMED AHMED, MBBS
Phone
33141880
Email
drnima88@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
YAHIA Z BASHIER IMAM, MBBS,MRCP,MRCPE
Organizational Affiliation
Hamad Medical Corporation
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hamad Medical Corporation
City
Doha
ZIP/Postal Code
3050
Country
Qatar
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
YAHIA Z BASHIER IMAM, MD,MRCP,MRCPE
Phone
55246887
Email
yimam@hamad.qa
First Name & Middle Initial & Last Name & Degree
NIMA K EL KHAWAD MOHAMED AHMED, MBBS
Phone
33141880
Email
drnima88@gmail.com
First Name & Middle Initial & Last Name & Degree
NUMAN AMIR, MB,BS
First Name & Middle Initial & Last Name & Degree
MAHER SAQQUR, FRCPC
First Name & Middle Initial & Last Name & Degree
AHMAD MUHAMMAD, MBBS
First Name & Middle Initial & Last Name & Degree
DIRK DELEU, PHD
First Name & Middle Initial & Last Name & Degree
AHMED OWN, MD
First Name & Middle Initial & Last Name & Degree
AHMED EL SOTOUHY, MD
First Name & Middle Initial & Last Name & Degree
ABDULSALIM KILIYANNI, MD
First Name & Middle Initial & Last Name & Degree
ABDUL SALAM, PHD
First Name & Middle Initial & Last Name & Degree
MOHAMED S ABDELMONEIM, MSC
First Name & Middle Initial & Last Name & Degree
PAULA BOURKE, PGC
First Name & Middle Initial & Last Name & Degree
DEBORAH MARGARET, BSC
First Name & Middle Initial & Last Name & Degree
MARK SANTOS, MAN
First Name & Middle Initial & Last Name & Degree
SUJATHA JOSEPH, MSC
First Name & Middle Initial & Last Name & Degree
pablo garcia, MD

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
32664066
Citation
Imam YZ, Mohamed MFH, Abdelmoneim MS, Santos M, Alkhawad N, Salam A, Amir N, Saqqur M, Muhammad A, Elsoutohy A, Kamran S, Akhtar N, Kiliyanni AS, Own A, Deleu D, Shuaib A. Prospective study to optimize the health of patients with TIAS (transient ischemic attack) and stroke admitted to the Hamad General Hospital. Medicine (Baltimore). 2020 Jul 10;99(28):e20694. doi: 10.1097/MD.0000000000020694.
Results Reference
derived

Learn more about this trial

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

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