Status:
COMPLETED
Exercise Capacity, Muscle Oxygenation, Respiratory Muscle Strength, and Physical Activity Level in Pediatric CF and PCD
Lead Sponsor:
Gazi University
Conditions:
Cystic Fibrosis (CF)
Primary Ciliary Dyskinesia (PCD)
Eligibility:
All Genders
6-18 years
Brief Summary
Cystic fibrosis (CF) and primary ciliary dyskinesia (PCD) are genetic diseases characterized by chronic respiratory tract infections. In both diseases, impaired mucociliary clearance, recurrent respir...
Detailed Description
In patients with cystic fibrosis (CF) and primary ciliary dyskinesia (PCD), lower extremity exercise capacity, skeletal muscle function, respiratory muscle strength, and physical activity levels are l...
Eligibility Criteria
Inclusion
- Cystic fibrosis patients;
- Patients diagnosed with cystic fibrosis according to the American Cystic Fibrosis Association consensus report
- Between the ages of 6 and 18
- Clinically stable conditions
- Primary ciliary dyskinesia patients;
- Patients diagnosed with primary ciliary dyskinesia according to the American Thoracic Society (ATS) and European Respiratory Society (ERS) guidelines
- Between the ages of 6 and 18
- Clinically stable conditions
- Healthy controls;
- Agreeing to participate voluntarily in the study
- Between the ages of 6 and 18
Exclusion
- Patients;
- Uncooperative
- Orthopedic or neurological disorders that will affect functional capacity
- Pneumonia or any acute infection
- Healthy controls;
- Chronic disease
- Uncooperative
- Orthopedic or neurological disorders that will affect functional capacity
Key Trial Info
Start Date :
January 1 2021
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
March 1 2025
Estimated Enrollment :
88 Patients enrolled
Trial Details
Trial ID
NCT07157644
Start Date
January 1 2021
End Date
March 1 2025
Last Update
September 5 2025
Active Locations (1)
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1
Gazi University Faculty of Health Sciences Department of Cardiopulmonary Physiotherapy and Rehabilitation
Ankara, Çankaya, Turkey (Türkiye), 06490