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
NA
200 participants
INTERVENTIONAL
2009-08-31
2013-01-31
Brief Summary
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Detailed Description
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With this purpose, a two-center randomized clinical trial, blinded for the endpoints re-hospitalization and costs, was designed.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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intervention and control
* Group I - Intervention: Routine follow-up in a reference health institution with four home visits and four telephone contacts with specialist nurses.
* Group II - Control: Routine follow-up with the health team in the reference institution.
Home Based Education
There will provided education about what is heart failure, its causes, how to recognize signs and symptoms, monitoring of weight and blood pressure, the importance of compliance to treatment. Patients will be instructed about the medications; a guide to rest and exercise, sexual activity, vaccines, travel and diet will be provided. The involvement of the family will be encouraged; the contact with the team should be done when: patient observes an increase of 1 or 2 kg of weight in 2-3 days, worsening of dyspnea on effort, edema in legs / abdomen, worsening of cough, persistent vomiting, syncope, sputum with blood, fever, persistent tachycardia. In phone calls made between home visits, the compliance to treatment will be evaluated and reinforced.
Interventions
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Home Based Education
There will provided education about what is heart failure, its causes, how to recognize signs and symptoms, monitoring of weight and blood pressure, the importance of compliance to treatment. Patients will be instructed about the medications; a guide to rest and exercise, sexual activity, vaccines, travel and diet will be provided. The involvement of the family will be encouraged; the contact with the team should be done when: patient observes an increase of 1 or 2 kg of weight in 2-3 days, worsening of dyspnea on effort, edema in legs / abdomen, worsening of cough, persistent vomiting, syncope, sputum with blood, fever, persistent tachycardia. In phone calls made between home visits, the compliance to treatment will be evaluated and reinforced.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Age equal to or above 18 years
* Diagnosis of heart failure with systolic dysfunction (ejection fraction ≤ 45%)
* Hospitalized for heart failure decompensation and who agree to participate in the study by signing a Free Informed Consent Form.
Exclusion Criteria
* Patients who had Acute Coronary Syndrome (ACS) in the past 6 months before randomization
* Patients with renal/hepatic/pulmonary or systemic disease who may confuse the interpretation of findings or result in limited life expectancy
* Surgical or therapeutic treatment that may influence the follow-up
* Pregnancy
* Diagnosis of Heart Failure secondary to:
* sepsis
* myocarditis
* acute myocardial infarction
* peripartum cardiomyopathy and other acute cause
* No interest in receiving home visits
* Living more than 10 km away for the original hospital
* No possibility of telephone contact.
18 Years
ALL
No
Sponsors
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Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul, Brazil
OTHER
Hospital de Clinicas de Porto Alegre
OTHER
Responsible Party
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Eneida Rejane Rabelo da Silva
Professor, PhD.
Principal Investigators
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Eneida R Rabelo da Silva, RN, ScD
Role: PRINCIPAL_INVESTIGATOR
Federal University of Rio Grande do Sul
Eneida R Rabelo da Silva, RN, ScD
Role: PRINCIPAL_INVESTIGATOR
Universidade Federal do Rio do Sul
References
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Mussi CM, Ruschel K, de Souza EN, Lopes AN, Trojahn MM, Paraboni CC, Rabelo ER. Home visit improves knowledge, self-care and adhesion in heart failure: Randomized Clinical Trial HELEN-I. Rev Lat Am Enfermagem. 2013 Jan-Feb;21 Spec No:20-8. doi: 10.1590/s0104-11692013000700004. English, Portuguese.
Other Identifiers
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UFRGS and HCPA 09111
Identifier Type: -
Identifier Source: org_study_id
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