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Determinants of Balance in Patients With Chronic Obstructive Pulmonary Disease

Completed
Conditions
Chronic Obstructive Pulmonary Disease
Registration Number
NCT05771506
Lead Sponsor
Biruni University
Brief Summary

The primary aim of our study is to examine the relationship between balance and respiratory function, respiratory and peripheral muscle strength, functional capacity, and cognitive function in patients with Chronic Obstructive Pulmonary Disease (COPD). The secondary aim of our study is to compare respiratory function, respiratory and peripheral muscle strength, functional capacity, balance, and cognitive functions of COPD patients and healthy individuals. This study will examine and record the participant's sociodemographic information and medical records. Balance, respiratory function, respiratory and peripheral muscle strength, functional capacity, and cognitive function will be assessed. Since the patients are included in this study, no intervention will be made, no additional tests will be performed, or no changes will be made in the routine treatments of the patients during the study.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
46
Inclusion Criteria
  • Being diagnosed with COPD in accordance with the GOLD criteria
  • Being between the ages of 40-65
  • To be able to speak, read, understand, and cooperate in Turkish
  • Being a volunteer to participate in the study

COPD Group

Exclusion Criteria
  • Having a COPD exacerbation in the last 8 weeks and/or having an unstable clinical condition
  • Having a diagnosed vision, hearing, or neurological disease that may affect balance
  • Having any other neurological, orthopedic, cardiovascular, thoracic, or metabolic disease or pathological condition that would affect assessments
  • Resting saturation below 90% during exercise tests
  • Being on long-term oxygen therapy

Control Group Inclusion Criteria:

  • Being between the ages of 40-65
  • To be able to speak, read, understand, and cooperate in Turkish
  • Being a volunteer to participate in the study

Control Group Exclusion Criteria:

  • Having a diagnosed vision, hearing, or neurological disease that may affect balance
  • Having any other neurological, orthopedic, cardiovascular, thoracic, or metabolic disease or pathological condition that would affect assessments
  • Resting saturation below 90% during exercise tests

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Maximal inspiratory pressure (MIP)15-20 minutes
Quadriceps muscle strength15-20 minutes
MoCA test10-15 minutes
FEV1/FVC10-15 minutes
6-minute walk test15-20 minutes
Sensory integration test of balance: Composite score20-30 minutes
Forced expiratory volume in 1 second (FEV1)10-15 minutes
Peak expiratory flow (PEF)10-15 minutes
Stability limits test: Overall score15-20 minutes
Maximal expiratory pressure (MEP)15-20 minutes
Postural stability test: Overall score15-20 minutes
Forced expiratory flow 25-75% (FEF25-75)10-15 minutes
Forced vital capacity (FVC)10-15 minutes
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Biruni University

🇹🇷

Istanbul, Turkey

Biruni University
🇹🇷Istanbul, Turkey

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