Completed

Comprehensive Rehabilitation Program Versus Traditional Chest Physiotherapy for Weaning From Mechanical Ventilator

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What is being tested

Comprehensive physical therapy rehabilitation program combined with inspiratory muscle training

+ Traditional chest physical therapy rehabilitation program combined with inspiratory muscle training

Other
Who is being recruted

From 40 to 50 Years
+10 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Interventional
Study Start: July 2019
See protocol details

Summary

Principal SponsorSherin Hassan Mohammed Mehani
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

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.

Official TitleComprehensive Rehabilitation Program Versus Traditional Chest Physiotherapy for Weaning From Mechanical Ventilator
NCT04021615
Principal SponsorSherin Hassan Mohammed Mehani
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

50 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

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

4 inclusion criteria required to participate
The general surgery patients who fail one weaning attempt of spontaneous breathing trial

Conscious patients

Hemodynamically stable patients (lack of hypotension or a need for only low-dose pressors)

The patients with Acute Physiology and Chronic Health Evaluation II (APACHE II) scale 20 or less

6 exclusion criteria prevent from participating
patients with persistent altered sensorium

patients with major cardiac arrhythmia

patients with comorbid medical conditions (e.g., neurological diseases) or who are under any sedative or paralytic agents that would interfere with strength measurements and limb exercises

patients with history of underlying neuromuscular disease or acquired polyneuromyopathies

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Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Twenty five patients will receive comprehensive rehabilitation program combined with inspiratory muscle training.

Group II

Active Comparator
Twenty five patients will receive traditional chest physical therapy combined with inspiratory muscle training.

Study 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

Suspended

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
CompletedOne Study Center