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Physical Impairments in Children With Cystic Fibrosis

NCT06984679 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2026-03-27

No results posted yet for this study

Summary

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.

Conditions

  • Cystic Fibrosis (CF)
  • Cystic Fibrosis in Children

Interventions

OTHER

Physical Evaluations in Children with Cystic Fibrosis

In this study, dyspnea, functional capacity, muscle strength, urinary incontinence and quality of life will be evaluated in children and adolescents with cystic fibrosis. The data to be obtained through all these evaluations will be done face to face within 45-60 minutes.

OTHER

Physical Evaluations in Healthy Children

In this study, dyspnea, functional capacity, muscle strength, urinary incontinence and quality of life will be evaluated in healthy children and adolescents. The data to be obtained from all these assessments will be made face to face within 45-60 minutes.

Sponsors & Collaborators

  • Izmir Democracy University

    lead OTHER

Principal Investigators

  • Gülşah Barğı, Assoc Prof · Izmir Democracy University

  • Yağmur Külekçi, PT · Izmir Democracy University

  • Gökçen Kartal Öztürk, Assoc Prof · Ege University

  • Ece Ocak, Dr · Izmir City Hospital

  • Kübra Özkaya, Dr · Ege University

Eligibility

Min Age
6 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-09-15
Primary Completion
2027-03-01
Completion
2027-03-03

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06984679 on ClinicalTrials.gov