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Sarcopenia in Patients With Idiopathic Pulmonary Fibrosis

Association of Sarcopenia With Quality of Life and Progression of Disease in Patients With Idiopathic Pulmonary Fibrosis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07178197
Enrollment
60
Registered
2025-09-17
Start date
2022-12-01
Completion date
2023-12-31
Last updated
2025-09-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Idiopathic Pulmonary Fibrosis (IPF), Sarcopenia

Keywords

idiopathic pulmonary fibrosis, sarcopenia, skeletal muscle mass index, bioelectrical impedance analysis

Brief summary

Sarcopenia negatively affects the prognosis of chronic diseases. However, the importance of sarcopenia in patients with idiopathic pulmonary fibrosis (IPF) has been less emphasized. The aim of the study is to determine the prevalence of sarcopenia in patients with IPF and to evaluate the impact of sarcopenia on quality of life and disease progression. This study was designed as a descriptive cross-sectional. The study included patients diagnosed with IPF. Hand dynamometry and bioelectrical impedance analysis (BIA) were used to for diagnose of sarcopenia. Pulmonary function tests, maximal inspiratory pressure (MIP), and maximal expiratory pressure (MEP) measurements were examined. The 6-minute walk distance (6MWD) and 4-meter walking speed were recorded. The St. George Respiratory Questionnaire (SGRQ) was used to assess quality of life. All patients were evaluated for progressive disease.

Detailed description

The study was designed as a cross-sectional study.

Interventions

None listed

Sponsors

Mersin University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Being over 18 years of age * Signing the informed consent form * Having a diagnosis of IPF for at least one month

Exclusion criteria

* Pregnancy * History of cancer within the last 5 years * History of lung surgery * History of neuromuscular disease * Active pulmonary tuberculosis * Active respiratory tract infection * Inability to perform pulmonary function tests * Presence of a pacemaker * History of systemic steroid use within the past 3 months * Inability to use a hand dynamometer

Design outcomes

Primary

MeasureTime frameDescription
Progressive Diseasethrough study completion, an average of 1 yearExamination of all participants from clinical, physiological, and radiological perspectives
Hand Grip Strengththrough study completion, an average of 1 yearHand Grip Strength (kg)- Grip strength measurement using a hand dynamometer
SMI (skeletal muscle mass index)through study completion, an average of 1 yearSMI (skeletal muscle mass index) (kg/m2) - SMI measurement using the Bioelectrical Impedance Analysis (BIA) device
Forced Expiratory Volume in 1 second (FEV1)through study completion, an average of 1 yearMeasurement of FEV1 for the assessment of pulmonary function
Forced Vital Capacity (FVC)through study completion, an average of 1 yearMeasurement of FVC for the assessment of pulmonary function
Diffusing Capacity of The Lungs for Carbon Monoxide (DLCO)through study completion, an average of 1 yearMeasurement of DLCO for the assessment of pulmonary function.
Total Lung Capacity (TLC)through study completion, an average of 1 yearMeasurement of TLC for the assessment of pulmonary function.
Respiratory Muscle Strengththrough study completion, an average of 1 yearMeasurement of maximal inspiratory pressure (MIP) and maximal expiratory pressure (MEP) for assessment of respiratory muscle strength
Six Minute Walk Test (6MWT)through study completion, an average of 1 yearDistance walked in six minutes (m)
Gait speedthrough study completion, an average of 1 year4-meter walking speed (m/s)
St. George's Respiratory Questionnaire (SGRQ)through study completion, an average of 1 yearThe questionnaire is designed to measure quality of life. It consists of symptom, activity, impact, and total scores. Each score ranges from 0 to 100. High scores indicate lower quality of life.

Secondary

MeasureTime frameDescription
Body Mass Index ( BMI)through study completion, an average of 1 yearkg/m2

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026