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

NCT ID: NCT04174664

Last Updated: 2019-11-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

26 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-11-01

Study Completion Date

2021-01-01

Brief Summary

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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.

Detailed Description

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This study will be participated children with cystic fibrosis who will diagnosed acute pulmonary exacerbation. Patients' pulmonary function test, functional capacity will be assess and record at hospital admission and hospital discharge and outpatient clinic control. Quality of life will be evaluated at only outpatient clinic control .

Pulmonary function test will be assessed with spirometry, functional capacity will be evaluated with 1-minute sit to stand test and 3-minute step test. And quality of life will be evaluated Cystic Fibrosis Questionnaire-Revised (CFQ-R).

Conditions

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Cystic Fibrosis in Children Exercise Capacity

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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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.

Intervention Type DIAGNOSTIC_TEST

Other Intervention Names

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3-minute step test Quality of life pulmonary function test

Eligibility Criteria

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Inclusion Criteria

* Childrens with CF diagnosed between 7-18 years of age and hospitalized due to acute pulmonary exacerbation will be included in the study.The diagnosis of acute pulmonary exacerbation will be established by Fuchs criteria.

Exclusion Criteria

* Patients with allergic bronchopulmonary aspergillosis (ABPA) who were treated with systemic steroid therapy and noninvasive mechanical ventilation support will not be included in the study.
Minimum Eligible Age

7 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hacettepe University

OTHER

Sponsor Role lead

Responsible Party

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Kübra Kılıç

MSc, PT

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Naciye Vardar-Yagli, PhD

Role: STUDY_DIRECTOR

Hacettepe University

Deniz Inal-Ince, Professor

Role: STUDY_CHAIR

Hacettepe University

Melda Saglam, PhD

Role: STUDY_CHAIR

Hacettepe University

Ebru Yalcin, Professor

Role: STUDY_CHAIR

Hacettepe University

Dilber Ademhan-Tural, MD

Role: STUDY_CHAIR

Hacettepe University

Kubra Kilic, MSc

Role: PRINCIPAL_INVESTIGATOR

Hacettepe University

Locations

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Hacettepe University

Ankara, , Turkey (Türkiye)

Site Status RECRUITING

Countries

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Turkey (Türkiye)

Central Contacts

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Kübra Kılıç, PhD Student

Role: CONTACT

+903123051576

Hacettepe University

Role: CONTACT

+903123051576

Facility Contacts

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Kubra Kilic, MsC

Role: primary

+903123051576

Hacettepe University

Role: backup

+903123051576

Other Identifiers

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GO 19/817

Identifier Type: -

Identifier Source: org_study_id

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