Muscle Endurance in Children With Cystic Fibrosis
NCT06812793 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 48
Last updated 2026-01-06
Summary
Cystic fibrosis (CF) is a genetic disorder affecting exocrine glands, leading to thick, viscous secretions that damage organs such as the lungs, pancreas, and reproductive system. Respiratory failure from CF lung disease is a major cause of morbidity and mortality, with chronic inflammation and infections disrupting mucociliary clearance. This results in declining respiratory functions, muscle strength, physical inactivity, and quality of life. While some studies compare respiratory and lower extremity muscle endurance in children with CF, none have evaluated core muscle endurance. This study aims to compare respiratory muscle strength, endurance, and muscle endurance in the core and lower extremities between children with CF and healthy peers.
Conditions
Interventions
- OTHER
-
Measurement of Core Muscle Endurance
Endurance of the flexor, extensor and lateral trunk muscles will be assessed using the McGill Trunk Endurance Tests.
- OTHER
-
Respiratory Muscle Strength
Inspiratory and expiratory muscle strength will be made with a portable, electronic intra-oral pressure measuring device.
- OTHER
-
Respiratory Muscle Endurance
Respiratory muscle endurance testing will be measured using an inspiratory muscle training device at increasing threshold load.
- OTHER
-
Peripheral Muscle Endurance
Peripheral muscle endurance will be assessed by performing 30 and 60 second sit-to-stand tests.
Sponsors & Collaborators
-
Bezmialem Vakif University
lead OTHER
Eligibility
- Min Age
- 6 Years
- Max Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2025-02-05
- Primary Completion
- 2025-11-03
- Completion
- 2025-12-29
Countries
- Turkey (Türkiye)
Study Locations
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