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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04161313
Other study ID # hdenizkulli2
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 20, 2019
Est. completion date March 12, 2020

Study information

Verified date March 2020
Source Bezmialem Vakif University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to compare pulmonary function, respiratory muscle strength, exercise capacity and peripheral muscle strength of patients with CF, PCD and healthy childrens.


Description:

The impaired airway clearence and pulmonary functions, exercise intolerance, low physical activity level and decreased peripheral muscle strength make physiotherapy approaches important in the management of CF and PCD.


Recruitment information / eligibility

Status Completed
Enrollment 76
Est. completion date March 12, 2020
Est. primary completion date February 24, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 6 Years to 18 Years
Eligibility Inclusion Criteria:

- Diagnosis of cystic fibrosis or primary ciliary dyskinesia

Exclusion Criteria:

- Hospitalization history in past month

- Diagnosis of other chronic pediatric diseases which may impair exercise tolerance such as cerebral palsy or neuromuscular disease

- Candidates for lung transplantation or history of lung transplantation

Study Design


Intervention

Other:
Measurement of functional capacity
Functional capacity of participants will be measured with six-minute walk test.
pulmonary function test
It will be measured using basic spirometry and presented lung volume parameters such as FEV1,FVC,FEV1/FVC,PEF, FEF25-75
Functional capacity
Functional capacity of participants will be measured with six-minute walk test and sit-to-stand test
Peripheral muscle strength
Isometric M. Quadriceps strength will be measured using electronic hand held dynamometer in sitting position.
Respiratory muscle strength
Inspiratory and expiratory muscle strength has been assessed by maximal inspiratory and expiratory mouth pressures.

Locations

Country Name City State
Turkey Bezmialem Vakif University Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Bezmialem Vakif University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Six-minute walk test distance Distance walked in six minutes will be recorded in meters. Test will be conducted according to the guideline of American Thoracic Society (ATS). 15 minutes
Secondary Forced Vital Capacity (FVC) FVC will be measured using basic spirometry and expressed as the percentage of the predicted value according to the guideline of European Respiratory Society (ERS) 5 minutes
Secondary Forced Expiratory Volume in 1 second (FEV1) FEV1 will be measured using basic spirometry and expressed as the percentage of the predicted value according to the guideline of European Respiratory Society (ERS) 5 minutes
Secondary Peak Expiratory Flow (PEF) PEF will be measured using basic spirometry and expressed as the percentage of the predicted value according to the guideline of European Respiratory Society (ERS) 5 minutes
Secondary M. Quadriceps strength Isometric M. Quadriceps strength (kg) will be measured using electronic hand held dynamometer in sitting position. 5 minutes
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