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Clinical Trials/NCT02312648
NCT02312648
Completed
N/A

Impact of an Early Mobilization Program on Functional Capacity After Coronary Artery Bypass Surgery: a Protocol of Randomized Controlled Trial.

Luciana Chiavegato0 sites52 target enrollmentJanuary 2015

Overview

Phase
N/A
Intervention
Not specified
Conditions
Postoperative; Dysfunction Following Cardiac Surgery
Sponsor
Luciana Chiavegato
Enrollment
52
Primary Endpoint
Functional Capacity
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The objective of this study is to investigate the effects of a program of early mobilization in the functional capacity in patients undergoing coronary artery bypass grafting in short and long- term.

Detailed Description

The hypotheses this study is that patients if conduct the program of early mobilization during hospitalization achieve better performance in the walk test (distance) at hospital discharge and 60 days after the surgical procedure compared to patients who only carry out the program of respiratory exercises. Intervention and control groups will receive breathing exercises up to 24 hours postoperatively, and the intervention group will also receive early mobilization exercises.

Registry
clinicaltrials.gov
Start Date
January 2015
End Date
November 2016
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Luciana Chiavegato
Responsible Party
Sponsor Investigator
Principal Investigator

Luciana Chiavegato

Professor of Master's and Doctoral Programs in Physical Therapy of Universidade Cidade de São Paulo

Universidade Cidade de Sao Paulo

Eligibility Criteria

Inclusion Criteria

  • Consecutive patients admitted to elective and conventional coronary artery bypass, Body Mass Index (BMI) between 20 and 30 Kg/m2, mechanical ventilation time under than 24 hours, hemodynamic stability with or without use of positive inotropes, absence of arrhythmias and angina, mean arterial pressure (MAP) 60\<PAM\<100 mmHg, heart frequency (HR) 60\<FC\<100 bpm without signs of respiratory distress such as flaring nose, use of accessory muscles, thoracoabdominal asynchrony, respiratory frequency (f) ≤ 20 bpm without signs of infection were included in this study.

Exclusion Criteria

  • : presence of previous pulmonary disease, ejection fraction under 35% or longer than 54%, reoperation, intraoperative death or any contraindications to perform the proposed measurements and/or treatment.

Outcomes

Primary Outcomes

Functional Capacity

Time Frame: All patients will be evaluated on preoperative period ( when they arrived in the hospital to do the surgery), hospital discharge ( about a mean of two weeks afeter surgery) and 60 postoperative days in cargiology ambulatory

Patients will be submitted to six minute walking test

Secondary Outcomes

  • Intensive Care Unit (ICU) and Hospital length of stay(All patients will be followed for the duration of hospital stay, an expected average of 30 days)
  • Postoperative pulmonary complication (PPC)(All patients will be followed for the duration of hospital stay, an expected average of 30 days)

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