Effect of the Active Cycle of Breathing Technique on Coronary Artery Bypass Graft Patients' Outcomes
1 other identifier
interventional
92
1 country
1
Brief Summary
Following CABG surgery, patients are at risk for several complications. One of the most common complications is postoperative pulmonary complications, which include atelectasis and dyspnea. These complications cause prolonged ICU length of stay and increased health care costs. Several studies recommended the active cycle of breathing technique as a method that increases secretion removal and improves lung functions, thus reducing the incidence of postoperative pulmonary complications. Our study aims to investigate the effect of the active cycle of breathing technique on coronary artery bypass graft patients' outcomes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jan 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 10, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 20, 2024
CompletedFirst Submitted
Initial submission to the registry
March 18, 2025
CompletedFirst Posted
Study publicly available on registry
April 4, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
May 25, 2025
CompletedJune 10, 2025
March 1, 2025
8 months
March 18, 2025
June 8, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (8)
Atelectasis
Atelectasis will be assessed using chest X-rays.
The first three postoperative days
Dyspnea
Dyspnea level will be assessed using the modified Borg scale.
The first three postoperative days
Functional capacity
Functional capacity will be assessed using the six-minute walk test
The first three postoperative days
Hemodynamic parameters
Hemodynamic parameters will include respiratory rate expressed as the number of cycles per minute, which will be assessed using the cardiac monitor
The first three postoperative days
Chest expansion
Chest expansion will be measured at three points (axillary, xiphoid point, and umbilical level) using a measuring tape in centimeters.
The first three postoperative days
Duration of chest tube
Duration of chest tube
Up to 1 week
Length of ICU stay
Measure the duration of the patient's ICU stay
For up to 1 week
Hemodynamic Parameters
Hemodynamic parameters will include oxygen saturation, which will be assessed using the pulse oximeter and will be expressed as a percentage %
For the first three postoperative days
Study Arms (2)
Active Cycle of Breathing Technique
EXPERIMENTALPatients who will perform ACBT exercises in addition to the routine ICU care.
Control Group
NO INTERVENTIONPatients who will receive routine ICU care (chest physiotherapy and incentive spirometer) without ACBT.
Interventions
* 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
You may qualify if:
- Any adult patient who will undergo CABG
You may not qualify if:
- Mechanically ventilated patients on the first postoperative day.
- Patients with preoperative lung collapse or pleural effusion.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Cardiothoracic and Vascular Surgery Center
Al Mansurah, Dakahliya, Egypt
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, OUTCOMES ASSESSOR
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Demonstrator of Critical Care and Emergency Nursing
Study Record Dates
First Submitted
March 18, 2025
First Posted
April 4, 2025
Study Start
January 10, 2024
Primary Completion
September 20, 2024
Study Completion
May 25, 2025
Last Updated
June 10, 2025
Record last verified: 2025-03