Determinants of Cardiac Risk Factor Modification in Latinos With Coronary Artery Disease
NCT ID: NCT00248859
Last Updated: 2017-02-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
198 participants
OBSERVATIONAL
2004-08-31
2010-06-30
Brief Summary
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Detailed Description
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1. To determine whether patients who have more depressive symptoms at the time of angioplasty are less likely to be active in physical activity at two years. Physical activity will be measured by a survey that asks patients to describe their activities including leisure activities or housework.
2. To determine whether lower perceived social support, lower self-efficacy for engaging in physical activity, and greater perceived stress mediate the effects of depressive symptoms on participation in physical activity.
Long-term objectives: The long-term objective of this study is to use these data to develop a culturally tailored intervention to increase participation in physical activity and ultimately improve the overall health and well being of Latino adults with coronary artery disease.
Outcome: The outcome is being in the action or maintenance stage of physical activity two years after angioplasty The stage of physical activity participation will be based on the Stages of Change model. This model describes behavior change as a continuum from pre-contemplation to contemplation.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Patients must be able to complete a questionnaire in either English or Spanish.
* Patients must have angiographic evidence of coronary artery disease requiring angioplasty
* Patients must also be clinically stable for an interview
* Patient must be able to provide informed consent.
Exclusion Criteria
* Patients who are unable to provide consent.
18 Years
ALL
Yes
Sponsors
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National Heart, Lung, and Blood Institute (NHLBI)
NIH
Weill Medical College of Cornell University
OTHER
Responsible Party
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Carla Boutin-Foster, MD
Study Principal Investigator
Principal Investigators
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Carla Boutin-Foster, MD
Role: PRINCIPAL_INVESTIGATOR
Weill Medical College of Cornell University
Locations
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Joan and Sanford I. Weill Medical College
New York, New York, United States
Countries
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Other Identifiers
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HL076567-01
Identifier Type: -
Identifier Source: org_study_id
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