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NCT Number: NCT07619716

ACBT With Incentive Spirometry Versus High-Frequency Chest Wall Oscillation After Thoracic Surgery

This randomized clinical trial aims to compare the effectiveness of Active Cycle of Breathing Techniques combined with Incentive Spirometry (ACBT + IS) versus High-Frequency Chest Wall Oscillation (HFCWO) in patients undergoing thoracic surgery. Postoperative pulmonary complications such as reduced lung function, ineffective cough, and sputum retention are common after thoracic procedures and can delay recovery. A total of 42 participants will be randomly allocated into two groups: one receiving ACBT with Incentive Spirometry and the other receiving HFCWO, along with standard postoperative care. Outcomes including cough effectiveness, sputum clearance, pulmonary function tests, and patient satisfaction will be assessed at baseline, postoperative day 3, and day 5. The study aims to determine the more effective airway clearance technique to improve respiratory outcomes and enhance patient recovery following thoracic surgery.

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Key information

Conditions

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Gulab Devi Hospital or General Hospital Lahore.

Lahore, Punjab Province, 40100, Pakistan

Location contact

Arjumand Bano, MS-CPPT

CONTACT

[email protected]

03059551883

Sarah Nasir, MS-CPPT

PRINCIPAL_INVESTIGATOR

About this study

Postoperative pulmonary complications are common after thoracic surgery due to reduced lung function and impaired secretion clearance. Effective respiratory physiotherapy is essential to improve recovery and prevent complications such as atelectasis and pneumonia.

This randomized clinical trial aims to compare the effectiveness of Active Cycle of Breathing Techniques combined with Incentive Spirometry (ACBT + IS) and High-Frequency Chest Wall Oscillation (HFCWO) in improving respiratory outcomes. A total of 42 patients undergoing elective thoracic surgery will be randomly assigned to either ACBT + IS or HFCWO, along with standard postoperative care.

Outcomes including cough effectiveness, sputum clearance, pulmonary function (FEV₁, FVC), and patient satisfaction will be assessed at baseline, postoperative day 3, and day 5. The study seeks to identify the more effective airway clearance technique to enhance recovery and reduce postoperative complications.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults aged 18-40 years
  • Patients scheduled for elective thoracic surgery (e.g., lobectomy, pneumonectomy, thoracotomy, or VATS)
  • Hemodynamically stable in the postoperative period
  • Cognitively and physically able to perform breathing exercises and use devices (incentive spirometer/HFCWO vest)
  • Willing to participate and provide informed consent

Exclusion criteria

  • Pre-existing severe pulmonary diseases (e.g., COPD, cystic fibrosis, bronchiectasis)
  • Contraindications to HFCWO (e.g., recent rib fractures, chest wall trauma, unstable cardiovascular status)
  • Cognitive, neuromuscular, or musculoskeletal impairments limiting participation in interventions
  • Prolonged mechanical ventilation (>24 hours postoperatively)
  • Active pulmonary infection or hemoptysis within one week after surgery

Treatment and study plan

Active Cycle of Breathing Techniques with Incentive Spirometry

Procedure

A structured breathing intervention combining Active Cycle of Breathing Techniques (breathing control, thoracic expansion exercises, and forced expiratory technique) with incentive spirometry to promote lung expansion and secretion clearance. Performed multiple times daily during the early postoperative period.

Other names: ACBT + IS

High-Frequency Chest Wall Oscillation

Device

A mechanical airway clearance technique delivered using an oscillatory vest that produces high-frequency chest wall vibrations to help mobilize and remove pulmonary secretions. The intervention is administered twice daily beginning on postoperative day 3.

Other names: HFCWO, Oscillatory Vest Therapy

Primary outcomes

  1. Forced Expiratory Volume in 1 second (FEV₁)

    Time frame: Baseline (preoperative), Postoperative Day 3, and Day 5

    Assessment of pulmonary function using spirometry parameters including Forced Expiratory Volume in 1 second (FEV₁) to evaluate respiratory recovery after thoracic surgery.

  2. Forced Vital Capacity (FVC)

    Time frame: Baseline (preoperative), Postoperative Day 3, and Day 5

    Assessment of pulmonary function using spirometry parameters including Forced Vital Capacity (FVC) to evaluate respiratory recovery after thoracic surgery.

  3. Cough Effectiveness

    Time frame: Baseline, Postoperative Day 3, and Day 5

    Evaluation of cough effectiveness using the Leicester Cough Questionnaire (LCQ), measuring physical, psychological, and social impact of cough.

Secondary outcomes

  1. Sputum Clearance

    Time frame: Postoperative Day 3 and Day 5

    Measurement of sputum volume to assess effectiveness of airway clearance techniques.

Study contacts

Contact information is provided by the study sponsor or research team.

Muhammad Iqbal Tariq, Phd*

CONTACT

[email protected]

03338236752

Sponsors and collaborators

Lead sponsor

Riphah International University

Other

Registry information

Official study title

Effects of Active Cycle of Breathing Techniques With Incentive Spirometry Versus High-Frequency Chest Wall Oscillation on Cough, Sputum, Pulmonary Function Test and Patient Satisfaction After Thoracic Surgery

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jun 2, 2026
Registry last updated
Jun 2, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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