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NCT07519460Not yet recruiting

Effects of High-Frequency Chest Wall Oscillation Combined With Concurrent Training on Cough,in Cystic Fibrosis Patients

Effects of High-Frequency Chest Wall Oscillation Combined With Concurrent Training on Cough, Sputum, Exercise Tolerance and Respiratory Muscle Strength in Cystic Fibrosis Patients

Source: ClinicalTrials.gov · Last updated 9 Apr 2026

Brief summary (registry, in English)

This randomized clinical trial aims to evaluate the effects of high-frequency chest wall oscillation (HFCWO) combined with concurrent training on cough, sputum clearance, exercise tolerance, and respiratory muscle strength in patients with Cystic Fibrosis. A total of 24 participants meeting inclusion criteria will be randomly allocated into two groups: Group A will receive HFCWO plus concurrent training, while Group B will receive HFCWO alone for 8 weeks. Outcomes will be measured before and after intervention using the 6-minute walk test, spirometry, Leicester Cough Questionnaire, sputum volume, and the Cystic Fibrosis Questionnaire-Revised. The study will be conducted at Pulmonary Rehabilitation Unit, Gulab Devi Hospital and Mayo Hospital, Lahore. Statistical analysis will be performed using IBM SPSS Statistics, with significance set at p \< 0.05.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
24 (estimated)
First submitted
2 Apr 2026
Start date
Apr 2026
Primary completion date
28 May 2026
Lead sponsor
Riphah International University
NCT number
NCT07519460

What you commit to

  • Study type: Interventional
  • Planned participants: 24
  • From Apr 2026 to the primary completion date, 28 May 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Acute airway infection.
  • Cognitive disorders affecting compliance.
  • Cardiac diseases such as heart failure or arrhythmias.
  • Neurological or orthopedic illnesses or recent chest injury.

Other

  • Active hemoptysis or pneumothorax.
  • Risk of hemodynamic instability or severe hypoxia.
  • Pregnancy.

Who the study is looking for

  • Diagnosed with Cystic Fibrosis, confirmed by genotype or sweat chloride \>60 mmol/L.
  • Age 16-35 years.
  • Both male and female participants.
  • Stable clinical condition (no exacerbations in the last 2 weeks).
  • Forced expiratory volume in 1 second (FEV₁ ≥ 20% predicted).

Age in the registry: 16 years to 35 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Gulab Devi Hospital, Mayo Hospital Lahore.
Coordinator of this site? Confirm its status
LahorePakistanUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.