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Study identifier: NCT07729787 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Autogenic Drainage Versus Mechanical Percussion in Children With Cystic Fibrosis

Condition: Cystic Fibrosis (CF)  ·  Sponsor: Riphah International University

PhaseNA
Planned participants32
Who can joinAll sexes, 6 Years to 12 Years
Healthy volunteersNo

About this study

The goal of this clinical trial is to compare the effects of autogenic drainage and mechanical percussion on lung function, dyspnea, and quality of life in children with cystic fibrosis. The main questions it aims to answer are: * Does autogenic drainage improve lung function more effectively than mechanical percussion in children with cystic fibrosis? * Does autogenic drainage reduce dyspnea (breathlessness) more effectively than mechanical percussion? * Does autogenic drainage improve health-related quality of life more effectively than mechanical percussion? Researchers will compare autogenic drainage with mechanical percussion to determine which airway clearance technique provides greater benefits for children with cystic fibrosis. Participants will: * Be randomly assigned to receive either autogenic drainage or mechanical percussion therapy. * Participate in supervised treatment sessions five times per week for six weeks. * Undergo assessments of lung function using spirometry (FEV₁ and FVC), dyspnea using the Modified Borg Dyspnea Scale, and quality of life using the Cystic Fibrosis Questionnaire-Revised (CFQ-R) before and after the intervention period. The findings of this study may help identify the most effective airway clearance technique for improving respiratory health and quality of life in children with cystic fibrosis.

This description comes directly from the study's public registry record.

Talk to the study team

Imran Amjad, PhD  ·  03324390125  ·  imran.amjad@riphah.edu.pk

Always discuss trial participation with your own doctor first.

Locations (1)

Nishter Hospital MultanMultan Khurd, Punjab Province, PakistanRecruiting

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Source record: clinicaltrials.gov/study/NCT07729787