Myocardial Infarction Clinical Trial
Official title:
Culturally-Tailored Hospital-based Model to Improve Statin Use and Outcomes in Patients With Coronary Disease
Verified date | January 2014 |
Source | Johns Hopkins University |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
Our research aims to improve the use of medicines known to prevent recurrent heart attacks.
In particular, we know that statin treatment is useful after heart attacks, but many
patients do not use it. There are a few possible reasons for this. Patients cannot find
affordable medicine. Their doctor may not prescribe the medicine after they leave the
hospital. Some people may culturally mistrust using the medicine. So they may decide not to
take it even if it is prescribed. We are developing a hospital based culturally attuned
program to target this problem. In this program, a community health worker counsels and
helps patients in accessing pharmacy assistance programs. We will test whether this program
can improve appropriate statin use.
We will enroll patients who have heart attacks. We will compare patients who are counseled
by the community health worker with those who get the usual care at baseline and at 6 and 12
months (participants enrolled during the early phase of the recruitment will have an
additional study visit at 24 months). We will test if their "bad" cholesterol levels are
controlled. We will find out how regularly they have filled their questionnaire and taken
the medicine. Finally, we will test if they are getting benefit from the statin treatment.
We will do this using blood tests and imaging the patients' arteries with ultrasound. We
will also measure how cost-effective it is for a hospital to run the program.
It is our goal to develop a community health worker model that is culturally sensitive for
people with cultural, educational or educational barriers. Statin use is known to benefit
patients in theory; such a culturally competent program will improve health outcomes in
practice. After we test it, a cost-effective program such as this can be implemented in
other hospitals.
Status | Completed |
Enrollment | 140 |
Est. completion date | December 2009 |
Est. primary completion date | December 2009 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 21 Years and older |
Eligibility |
Inclusion Criteria: - Admitted to Johns Hopkins Hospital or Johns Hopkins Bayview Medical Center - Diagnoses of Myocardial Infarction, unstable angina, percutaneous intervention, coronary artery bypass surgery - One of the following: - Less than a high school education (defined as completion of the 12th grade) - No insurance for medications with a household income of $50,000. or less - Any difficulty in co-pay even with a household income of >$50,000. Exclusion Criteria: - physician contraindicates statin use - chronic glucocorticosteroid therapy - autoimmune disease (i.e. lupus erythematosus) - current chemotherapy or radiation - immediate life-threatening comorbidity (i.e. HIV-AIDS, end-stage renal disease, or cancer) - history of hepatic or renal failure - myositis with creatine kinase (CK) elevations - any prior adverse response to statin therapy - statin allergy - rhabdomyolysis - pregnant women |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
United States | Johns Hopkins Hospital | Baltimore | Maryland |
Lead Sponsor | Collaborator |
---|---|
Johns Hopkins University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Achievement of LDL-cholesterol Goals | Achieving the goal of an LDL cholesterol level of < 100 mg/dL. For intention to treat analysis the randomization visit status is carried forward if data are missing for the 6-month follow-up visit. | 6 months | No |
Secondary | Self-reported Medication Adherence | Only individuals with 6-month follow-up data were included in this analysis | 6 months | No |
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