Effect of the Active Cycle of Breathing Technique on Coronary Artery Bypass Graft Patients' Outcomes
NCT ID: NCT06910020
Last Updated: 2025-06-10
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
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
92 participants
INTERVENTIONAL
2024-01-10
2025-05-25
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effects of Balance Training on Functional Capacity of Patients After Coronary Artery Bypass Grafting Surgery
NCT06490458
Power Lung Versus Acapella After Coronary Artery Bypass Graft Surgery
NCT05260944
The Effects of Neurophysiological Facilitation Techniques After Coronary Artery Bypass Graft Surgery
NCT06640699
High Frequency Ventilation During Off Pump Coronary Artery Bypass Graft (CABG)
NCT00863044
The Effects of Cardiac Rehabilitation on Sleep Quality and Sleep Duration in Patients After Coronary Artery Bypass Graft
NCT05474339
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
PREVENTION
TRIPLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Active Cycle of Breathing Technique
Patients who will perform ACBT exercises in addition to the routine ICU care.
Active Cycle of Breathing Technique
* Patients will assume the sitting position and relax their shoulders, then perform the following:
1. Breathing control (abdominal breathing)
2. Chest expansion (thoracic breathing)
3. Huff cough (forced expiratory technique)
* After completing the above actions, patients will be asked to cough up the residual deep sputum to promote pulmonary expansion.
* The ACBT intervention will be performed for three days, each day two sessions, each session three courses, with 10 minutes of rest between them as needed.
Control Group
Patients who will receive routine ICU care (chest physiotherapy and incentive spirometer) without ACBT.
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Active Cycle of Breathing Technique
* Patients will assume the sitting position and relax their shoulders, then perform the following:
1. Breathing control (abdominal breathing)
2. Chest expansion (thoracic breathing)
3. Huff cough (forced expiratory technique)
* After completing the above actions, patients will be asked to cough up the residual deep sputum to promote pulmonary expansion.
* The ACBT intervention will be performed for three days, each day two sessions, each session three courses, with 10 minutes of rest between them as needed.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* Patients with preoperative lung collapse or pleural effusion.
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Mansoura University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Shaimaa Nagi Abdelkader Yousef
Demonstrator of Critical Care and Emergency Nursing
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Cardiothoracic and Vascular Surgery Center
Al Mansurah, Dakahliya, Egypt
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
320
Identifier Type: REGISTRY
Identifier Source: secondary_id
320
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.