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Impact of Nursing Systematic Orientations in Reduction of the Risk Estimate of Cardiovascular Events (NERRECE)
This study is enrolling participants by invitation only.
Sponsored by: Hospital de Clinicas de Porto Alegre
Information provided by: Hospital de Clinicas de Porto Alegre
ClinicalTrials.gov Identifier: NCT00795626
  Purpose

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
Coronary Heart Disease
Behavioral: Systematic education in the reduction of the risk estimate to cardiovascular events

MedlinePlus related topics: Coronary Artery Disease Heart Diseases
U.S. FDA Resources
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

Further study details as provided by Hospital de Clinicas de Porto Alegre:

Primary Outcome Measures:
  • Reduction of the risk estimate to cardiovascular events [ Time Frame: one year ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Knowledge of the risk factors and the adhesion to pharmacology treatment; - Reduction of the modified risk factors in the previous knowledge of patients and their adhesion; [ Time Frame: one year ]

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
Lifestyle counseling: Experimental

Two groups:

  • control - conventional care
  • intervention - systematic education in the reduction of the risk estimate to cardiovascular events
Behavioral: Systematic education in the reduction of the risk estimate to cardiovascular events
Systematic education during 4 assessment throughout one year

Detailed Description:

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:

  • To evaluate the knowledge of the risk factors and the adhesion to pharmacology treatment during the basal period and after one year in both groups;
  • To compare the reduction of the modified risk factors in the previous knowledge of patients and their adhesion to the treatment in both groups;
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

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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  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00795626

Locations
Brazil, Rio Grande do Sul
Eneida Rejane Rabelo
Porto Alegre, Rio Grande do Sul, Brazil, 90035003
Sponsors and Collaborators
Hospital de Clinicas de Porto Alegre
Investigators
Principal Investigator: Eneida R Rabelo, RN, ScD Federal University of Rio Grande do Sul Post Grad Prog
  More Information

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

Keywords provided by Hospital de Clinicas de Porto Alegre:
nursing education
cardiovascular risk factors
coronary heart disease

Study placed in the following topic categories:
Arterial Occlusive Diseases
Coronary Disease
Heart Diseases
Myocardial Ischemia
Vascular Diseases
Arteriosclerosis
Ischemia
Coronary Artery Disease

Additional relevant MeSH terms:
Cardiovascular Diseases

ClinicalTrials.gov processed this record on January 14, 2009