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Sponsored by: |
Hospital de Clinicas de Porto Alegre |
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Information provided by: | Hospital de Clinicas de Porto Alegre |
ClinicalTrials.gov Identifier: | NCT00795626 |
The nursing systematic orientations in patients with coronary artery disease, who have been observed during 4 nursing consultations throughout one year, compared to a group of patients in a conventional treatment reduced the risk estimate to cardiovascular events.
Condition | Intervention |
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Coronary Heart Disease |
Behavioral: Systematic education in the reduction of the risk estimate to cardiovascular events |
Study Type: | Interventional |
Study Design: | Supportive Care, Randomized, Open Label, Efficacy Study |
Official Title: | Impact of Nursing Sistematic Orientations in Reduction of the Risk Estimate of Cardiovascular Events in Patients With Coronary Artery Disease |
Estimated Enrollment: | 184 |
Study Start Date: | January 2007 |
Estimated Study Completion Date: | January 2011 |
Estimated Primary Completion Date: | January 2008 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
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Lifestyle counseling: Experimental
Two groups:
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Behavioral: Systematic education in the reduction of the risk estimate to cardiovascular events
Systematic education during 4 assessment throughout one year
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To evaluate the impact of nursing systematic orientations by a systematic education in the reduction of the risk estimate to cardiovascular events in patients with coronary artery disease, who have been observed during 4 nursing consultations throughout one year, compared to a group of patients in a conventional treatment.
Specific Objectives:
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:patients of both sexes, over 18 years old, with diagnostic of ACS (unstable angina and acute myocardial infarctation (AMI) with elevation of. ST segment and without elevation of ST segment) with CAD diagnosticated by cardiac catheterism or electrocardiogram, and they must agree to participate in the study by signing the term of consent presented to them. All patients described above are going to be invited to participate in the study still in their hospitalization, however the first nursing assessment is going to be booked for the third month after discharge. This period is justified because the first three months are considered to be a critical period to occur new events and complications.
Exclusion Criteria:those patients with cognitive déficits, neurological sequelas, who do not have availability to come to the consultations or not agree to participate in this study.
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Brazil, Rio Grande do Sul | |
Eneida Rejane Rabelo | |
Porto Alegre, Rio Grande do Sul, Brazil, 90035003 |
Principal Investigator: | Eneida R Rabelo, RN, ScD | Federal University of Rio Grande do Sul Post Grad Prog |
Responsible Party: | Post Graduated Program in Cardiovascular Science ( Federal University of Rio Grande do Sul ) |
Study ID Numbers: | UFRGS and HCPA 06570 |
Study First Received: | November 20, 2008 |
Last Updated: | November 20, 2008 |
ClinicalTrials.gov Identifier: | NCT00795626 |
Health Authority: | Brazil: National Committee of Ethics in Research |
nursing education cardiovascular risk factors coronary heart disease |
Arterial Occlusive Diseases Coronary Disease Heart Diseases Myocardial Ischemia |
Vascular Diseases Arteriosclerosis Ischemia Coronary Artery Disease |
Cardiovascular Diseases |