Comprehensive Rehabilitation Program Versus Traditional Chest Physiotherapy for Weaning From Mechanical Ventilator
Comprehensive physical therapy rehabilitation program combined with inspiratory muscle training
+ Traditional chest physical therapy rehabilitation program combined with inspiratory muscle training
Treatment Study
Summary
Study start date: July 21, 2019
Actual date on which the first participant was enrolled.This study focuses on improving the weaning process from mechanical ventilators for critically ill patients. Prolonged immobility in the ICU can lead to functional losses, reduced quality of life, and increased healthcare costs. The European Respiratory Society and European Society of Intensive Care Medicine have suggested a hierarchy of ICU mobilization to combat these issues. Weaning from mechanical ventilators as early as possible is crucial to avoid further complications. This study introduces a Targeted Mobility Therapy (TMT), a novel strategy that includes inspiratory muscle strength training, bronchial hygiene, and active mobilization, aiming to improve weaning success, reduce days on mechanical ventilators, shorten hospital stays, and enhance functional mobility. During the study, the mechanical ventilator will measure the plateau pressure (maximal inspiratory pressure) to assess inspiratory muscle strength. Spontaneous breathing trials will be conducted when the underlying cause of acute respiratory failure stabilizes or significantly improves. These trials can last from 30 minutes to 120 minutes, combined with CPAP. If a trial fails, the patient will return to full ventilatory support for at least 24 hours before a new trial is performed. Weaning success is defined as extubation and the absence of ventilatory support 48 hours following extubation.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.50 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 40 to 50 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
Active ComparatorStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
surgical intensive care unit, Kasr Al Ainy Teaching Hospital, Cairo University and Beni- Suef Teaching Hospital , Beni -Suef University.
Cairo, EgyptOpen surgical intensive care unit, Kasr Al Ainy Teaching Hospital, Cairo University and Beni- Suef Teaching Hospital , Beni -Suef University. in Google Maps