Stroke Clinical Trial
— PROTECT DCOfficial title:
Preventing Recurrence of Thromboembolic Events Through Coordinated Treatment in the District of Columbia
Verified date | February 2013 |
Source | Georgetown University |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Federal Government |
Study type | Interventional |
The purpose of this study is to refine and evaluate the Preventing Recurrence of Thromboembolic Events through Coordinated Treatment in the District of Columbia (PROTECT DC) intervention. PROTECT DC is a program consisting of in-hospital education coupled with community-based "stroke navigators" and is designed to reduce the rate of vascular events or death in a population of underserved individuals with stroke.
Status | Completed |
Enrollment | 230 |
Est. completion date | January 2013 |
Est. primary completion date | January 2013 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Age = 18 years - Hospitalized due to ischemic stroke* or intercurrent ischemic stroke* event within the past 30 days OR Transient ischemic attack, confirmed by stroke neurologist. - Atherogenic etiology(large vessel, small vessel, cryptogenic with at least one stroke risk factor, or embolic stroke due to atherogenic cardiac disease) as defined by TOAST criteria. - Community dwelling prior to stroke - Resides within the District of Columbia or closely nearby (preferably within 10 miles of the DC border) - Expected to reside within the District of Columbia or closely nearby (preferably within 10 miles of DC border) - Caregiver or interested party available, if moderately or severely disabled (not required to actually reside with participant) - Sufficient number of collateral contacts to assure follow-up. Defined as: Preferred: at least 6 contacts; and No fewer than 3 contacts (unless approved by study PI/co-PI/co-I) - Judged likely to return to community setting at completion of post-acute care. Exclusion Criteria: - Non-atherogenic cause of stroke - NIHSS > 20 - Any medical condition that would limit participation in follow up assessments - Baseline dementia per informant report (AD8) or screening assessment (Short Blessed Memory Orientation Concentration Test) |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care
Country | Name | City | State |
---|---|---|---|
United States | George Washington University Hospital | Washington | District of Columbia |
United States | Georgetown University Hospital | Washington | District of Columbia |
United States | Howard University Hospital | Washington | District of Columbia |
United States | National Rehabilitation Hospital | Washington | District of Columbia |
United States | Providence Hospital | Washington | District of Columbia |
United States | Washington Hospital Center | Washington | District of Columbia |
Lead Sponsor | Collaborator |
---|---|
Georgetown University | National Institute of Neurological Disorders and Stroke (NINDS) |
United States,
Dromerick AW, Gibbons MC, Edwards DF, Farr DE, Giannetti ML, Sánchez B, Shara NM, Fokar A, Jayam-Trouth A, Ovbiagele B, Kidwell CS. Preventing recurrence of thromboembolic events through coordinated treatment in the District of Columbia. Int J Stroke. 2011 Oct;6(5):454-60. doi: 10.1111/j.1747-4949.2011.00654.x. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Low Density Lipoprotein Value | 1 year | No | |
Primary | Systolic Blood Pressure Value | 1 year | No | |
Primary | Hemoglobin A1C Value | 1 year | No | |
Primary | Pill count of antiplatelet therapy medications | 1 year | No | |
Secondary | Smoking Cessation Status | 1 year | No | |
Secondary | AHA Diet Status | 1 year | No | |
Secondary | Exercise Status | 1 year | No | |
Secondary | Stroke Knowledge Level | 1 year | No |
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