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Recruiting NCT06258681

Customizable Respiratory Exercise Device in Individuals Who Have Undergone Cardiac Surgery

No phase Interventional Coronary Artery Disease

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Incentive spirometer, Individualized respiratory training group.
Who it may be relevant to
Registry conditions: Coronary Artery Disease. Basic parameters: 40 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Examining the Clinical Efficiency of a Customizable Respiratory Exercise Device in Individuals Who Have Undergone Cardiac Surgery

Overview

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.

Detailed description

Breathing exercises can be applied specifically to different segments of the lungs, increasing collateral ventilation and helping mobilize secretions. Chronic respiratory diseases, rib cage deformities, neuromuscular diseases that cause breathing problems, lung transplant or lung surgery patients in the pre-operative and post-operative period, cancer patients, heart failure patients and cardiovascular surgery patients, and those whose quality of life is impaired due to shortness of breath. People are known to be groups that benefit from breathing exercises. Breathing exercises have been shown to be effective in preserving respiratory function and preventing or reducing respiratory complications in all of these conditions. It has been reported that respiratory muscle training applied within the scope of pre- and post-operative cardiac rehabilitation programs is beneficial in increasing respiratory functions and reducing the risk of postoperative 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 inspiratory and expiratory muscles, and each training method and device has differences. For this reason, the respiratory exercise device to be developed is aimed to be a device that can be shaped according to the desired purpose, has visual feedback, and can combine multiple respiratory muscle training methods. The device is thought to play an active role in rehabilitating complications such as lung ventilation and respiratory muscle weakness, which are frequently affected in patients after major surgery such as cardiac surgery. 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.

Interventions

  • Other Incentive spirometer
    The incentive spirometry group will continue training with Volumetric Triflo. It is asked to exhale at first and then hold their breath for at least 3 seconds after taking as deep a breath as possible.
  • Other Individualized respiratory training group
    Participants will be able to practice both inspiratory and expiratory respiratory muscle training in a single breathing cycle.

Primary outcome measures

  • The Forced Expiratory Volume 1st second [Time frame: 8 weeks]
  • Forced Vital Capacity [Time frame: 8 weeks]
  • Peak Expiratory Flow [Time frame: 8 weeks]
  • Respiratory Muscle Strength [Time frame: 8 weeks]
  • Six minutes walking test [Time frame: 8 weeks]
Secondary outcome measures (1)
  • Minnesota Life with Heart Failure Questionnaire. [Time frame: 8 weeks]

Eligibility criteria

Inclusion criteria

  • Individuals with New York Heart Association Functional Class I or II who are scheduled to undergo elective coronary artery bypass graft surgery, aortic valve replacement, mitral valve replacement, or combined surgery of aortic and mitral valve replacement
  • Individuals who are planning to undergo surgery with the median sternotomy technique
  • Individuals with Mini-Mental State Score >24

Exclusion criteria

  • Individuals with uncontrolled arrhythmia, unstable angina pectoris, uncontrolled hypertension
  • Individuals with accompanying chronic respiratory disease
  • Individuals with accompanying neuromuscular or orthopedic/musculoskeletal limitations
  • Individuals with a history of spontaneous or trauma-related pneumothorax
  • Individuals with middle ear-related pathologies (such as tympanic membrane rupture otitis)
  • Cases with thorax drains in the ward
  • Individuals who stayed in the intensive care unit for ≥ 4 days in the postoperative period
  • Individuals who have had another surgery in the last six months

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Treatment

Study locations

Turkey (Türkiye) · 1 center
  • Istanbul Florence Nightingale Hospital — Istanbul

Publications

  • Eksi BU, Cilbir CE, Ucgun H, Ertan Harputlu O, Aslan GK, Ezelsoy M, Ugurlucan M, Sagbas LE, Akinci B. Effects of integrated inspiratory-expiratory muscle training within hybrid cardiac rehabilitation following cardiac surgery: A randomized controlled study. Respir Med. 2026 Jul 1;261:109018. doi: 10.1016/j.rmed.2026.109018. Online ahead of print. PMID 42386010

Identifiers

NCT: NCT06258681 · 682201

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗