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Muscle Strength, Functional Capacity, Respiratory Function and Quality Of Life In Cystic Fibrosis Patients

C

Cagtay Maden

Status

Completed

Conditions

Pulmonary Function
Functional Capacity
Muscle Strength
Muscular Endurance
Exercise Tolerance
Cystic Fibrosis

Treatments

Other: cystic fibrosis

Study type

Interventional

Funder types

Other

Identifiers

NCT04734743
2016/06

Details and patient eligibility

About

This study was designed to investigate the relationship between upper extremity muscle strength and endurance, functional capacity, and quality of life child and adolescent with cystic fibrosis

Full description

Child and adolescent with cystic fibrosis patients were assessed for upper extremity muscle strength and (Shoulder abductors muscle strength, Elbow flexion muscle strength, Handgrip strength) muscular endurance(arm pull-up test), lung function test, and functional capacity (six-minute walk test distance), and Quality Of Life (Cystic Fibrosis Questionnaire-Revised)

Enrollment

63 patients

Sex

All

Ages

6 to 15 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Individuals diagnosed with CF with clinical findings and gene mutations consistent with CF, having over 60mEq / L in two measurements in sweat chlorine examinations

Exclusion criteria

  • Patients who did not exacerbate the disease in the last four weeks, who had good cooperation and did not have any orthopedic problems in the hand-shoulder-arm complex were included.

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

63 participants in 1 patient group

Cystic fibrosis
Other group
Treatment:
Other: cystic fibrosis

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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