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NCT00013741 Clinical Trial

The MI-HEART Project

Myocardial Infarction Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00013741
Other study ID # 9511
Secondary ID N01LM93534
Status Completed
Phase N/A
First received March 28, 2001
Last updated May 23, 2012

Study information
Verified date February 2003
Source National Library of Medicine (NLM)
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

The purpose of the study is to examine ways in which a clinical information system can help patients better recognize the signs and symptoms of an acute myocardial infarction (heart attack) and to take actions to decrease morbidity and mortality that may be related to delay in seeking treatment. The software-based intervention will use the best scientific evidence to create tailored strategies using a patient's specific health data. This approach is based on well-established cognitive and behavioral educational models.

Recruitment information / eligibility
Status Completed
Enrollment 55
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 30 Years and older
Eligibility Inclusion Criteria

- Patients at high-risk for an acute myocardial infarction, including any 2 of these risk factors: males age > 45; females age >55; family history of premature coronary heart disease (CHD); current cigarette smoker; hypertension; or elevated total cholesterol with low HDL and/or high LDL.

OR have:

- Active angina (chest pain due to coronary heart disease)

- History of coronary heart disease according to the treating physician

- Past history of myocardial infarction documented by electrocardiogram or arteriography

- Diabetes Mellitus

- Renal dialysis

Exclusion Criteria

- Hospitalization within previous 4 weeks

- Persons living in a home with previously enrolled patients

- Patients disoriented to person, place, or time at onset of study

Study Design

Allocation: Randomized, Masking: Double-Blind

Related Conditions & MeSH terms

Intervention

Behavioral:
• Tailored Education Messages

Locations
Country Name City State
United States Columbia University, Department of Medical Informatics New York New York

Sponsors (1)
Lead Sponsor Collaborator
National Library of Medicine (NLM)

Country where clinical trial is conducted

United States, 

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