CompletedNot Applicable

Supervised vs Non-Supervised Incentive Spirometry After CABG

Indonesia38 participantsStarted 2024-07-01

Plain-language summary

This study aims to evaluate the effect of supervised incentive spirometry (SIS) compared to unsupervised incentive spirometry (Non-SIS) on pulmonary function in patients following coronary artery bypass graft (CABG) surgery. Participants perform incentive spirometry exercises twice daily for three days after extubation. Pulmonary function parameters, including forced expiratory volume in one second (FEV1), forced vital capacity (FVC), and peak expiratory flow (PEF), are assessed before and after the intervention period to compare changes between the two groups.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Adult patients aged ≥18 years. * Patients who have undergone Coronary Artery Bypass Graft (CABG) surgery. * Mechanical ventilation \<24 hours post-surgery. * Physically able to perform incentive spirometry (IS) exercises. * Signed informed consent to participate in the study. Exclusion Criteria: * Hemodynamically unstable patients. * Patients with cognitive or communication impairments. * Oral abnormalities that prevent the use of IS. * Patients with Chronic Obstructive Pulmonary Disease (COPD). * Patients with thoracic anomalies. * Patients who required reintubation. * History of incentive spirometry use within the last 3 months.

What they're measuring

Forced Expiratory Volume in 1 Second (FEV1)

Timeframe: T1 (24 hours post-extubation) and T2 (after 3 days of incentive spirometry exercise)

Trial details

NCT IDNCT07343921

SponsorUniversitas Padjadjaran

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-12-01

View on ClinicalTrials.gov More Postoperative Pulmonary Function Impairment trials