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Comparison of Different Functional Capacity Tests in Cystic Fibrosis Patients With Acute Pulmonary Exacerbation

NCT04174664 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 26

Last updated 2019-11-22

No results posted yet for this study

Summary

The aim of this study to investigate and compare functional capacity with different tests and to evaluate the relationship between functional capacity and quality of life during acute pulmonary exacerbation in children with cystic fibrosis.

Exercise tests associated with prognostic values in CF patients and decreased exercise capacity has been correlated with a reduction in health-related quality of life. Pulmonary functions, functional capacity and quality of life will examine in this study.

Conditions

  • Cystic Fibrosis in Children
  • Exercise Capacity

Interventions

DIAGNOSTIC_TEST

1-minute sit to stand test

Childrens will complete 1-minute sit to stand test and 3 minute step test and quality of life questionnaire.

Sponsors & Collaborators

  • Hacettepe University

    lead OTHER

Principal Investigators

  • Naciye Vardar-Yagli, PhD · Hacettepe University

  • Deniz Inal-Ince, Professor · Hacettepe University

  • Melda Saglam, PhD · Hacettepe University

  • Ebru Yalcin, Professor · Hacettepe University

  • Dilber Ademhan-Tural, MD · Hacettepe University

  • Kubra Kilic, MSc · Hacettepe University

Eligibility

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

Timeline & Regulatory

Start
2019-11-01
Primary Completion
2021-01-01
Completion
2021-01-01

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 NCT04174664 on ClinicalTrials.gov