- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00013741
The MI-HEART Project
May 23, 2012 updated by: National Library of Medicine (NLM)
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment
55
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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New York
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New York, New York, United States
- Columbia University, Department of Medical Informatics
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
30 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Allocation: Randomized
- Masking: Double
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: James J. Cimino, M.D., Columbia University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Registration Dates
First Submitted
March 28, 2001
First Submitted That Met QC Criteria
March 29, 2001
First Posted (Estimate)
March 30, 2001
Study Record Updates
Last Update Posted (Estimate)
May 24, 2012
Last Update Submitted That Met QC Criteria
May 23, 2012
Last Verified
February 1, 2003
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 9511
- N01-LM-93534
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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