Heart Failure Clinical Trial
Official title:
Safety and Efficacy of Exercise Training in Patients With Acute Heart Failure: a Pilot Study
This project deals with exercise in acute heart failure in three different groups (conventional medical treatment; exercise with non-invasive ventilation and exercise with placebo of non-invasive ventilation).
All of the subjects performed an individualized clinical evaluation right after hospital
admission on day 1 (D1) by the cardiologist and physiotherapis involved in the study.
Pulmonary function tests (spirometry), blood sample (brain natriuretic peptide [NT-proBNP]
and high sensitive C-reactive protein [hs-CRP]), six-minute walk test (6MWT), and maximal
inspiratory pressure (MIP) test were performed.
After the clinical tests were performed, the patients were randomized into three groups, and
all received standard medical treatment.
The control group (CTL) received medical treatment and did not perform aerobic exercise
training; the ET+NIV group performed aerobic exercise training associated with NIV once a
day, for 8 consecutive days; and the ET+Sham group performed aerobic exercise with placebo
NIV once a day, for 8 consecutive days. The ET+NIV and ET+Sham groups also received medical
treatment.
After eight consecutive days, all of the patients underwent a new clinical evaluation (D10).
After D10, all of the patients continued to receive only conventional treatment, and they
were followed up for main outcomes (hospital discharge, worsening HF, or death). Worsening
HF was considered when a patient needed to be transferred to the intensive care unit.
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
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