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Customizable Respiratory Exercise Device in Individuals Who Have Undergone Cardiac Surgery

StatusRecruiting
PhaseNot applicable
Started2024-02-28
View on ClinicalTrials.gov ↗
Record status
This record was last updated February 7, 2025 (before its estimated May 30, 2025 completion). Its status may not reflect the trial's current state.

Amendment history

2025-02-05
notable
Not Yet Recruiting→Recruiting Study Status, Oversight, Contacts/Locations v1
Trial statusNot Yet Recruiting→Recruiting
Study sites0→1
2024-02-12
minor
Original filing
The cardiorespiratory system integrates systemic and pulmonary circulation while ensuring adequate oxygenation of the body at rest and during exercise. In addition to chronic respiratory problems that mainly affect the lungs, airways and pulmonary vascular system, respiratory capacity and respiratory muscle strength can be negatively affected in a wide spectrum including cardiac diseases, surgeries, neuromuscular diseases, obesity, long-term bed rest, aging and inactivity. Weakness of the respiratory muscles causes important secondary consequences by causing the increased respiratory demands not to be met during physical activity. It has been reported that respiratory muscle training applied within the scope of pre-operative and post-operative cardiac rehabilitation program is beneficial in terms of increasing respiratory functions, reducing the risk of post-operative complications and length of stay. Respiratory muscle training is known to have many potential beneficial effects on patients undergoing cardiac surgery. Different methods and devices are used to improve and develop the functions of the inspiratory and expiratory muscles and each training method and device has differences. Therefore, it is thought that examining the clinical effects of using a personalized breathing exercise device on respiratory functions, respiratory muscle strength and functional capacity in individuals who have undergone cardiac surgery will contribute to the literature.
Trial Details
NCT Number NCT06258681
Lead Sponsor Biruni University
Collaborators: Istanbul Galata University
Conditions Coronary Artery Disease
Enrollment 20 participants
Start Date 2024-02-28
Primary Completion 2025-05-30 (estimated)
Study Completion 2025-05-30 (estimated)
Updated on ClinicalTrials.gov 2025-02-07