Comparison of Dyspnea, Functional Capacity, Muscle Strength, Urinary Incontinence and Quality of Life Between Children and Adolescents With Cystic Fibrosis and Healthy Children
It is aimed to reveal impairments regarding urinary incontinence, dyspnea, muscle strength, functional capacity or quality of life in children and adolescents with cystic fibrosis compared to healthy children and adolescents.
• To be between the ages of 6-18
• To have been diagnosed with cystic fibrosis
• To be clinically stable for at least 3 weeks
• To have the necessary cooperation for the measurements
• To volunteer to participate in the study
• To be between the ages of 6-18
• To be in a similar average and ratio with the group of children and adolescents with cystic fibrosis in terms of age and gender
• To have the necessary cooperation for the measurements
• To volunteer to participate in the study