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Determination of Factors Related With Daily Living Activities in Severe COPD

H

Halic University

Status

Completed

Conditions

COPD

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The main purpose of chronic obstructive pulmonary disease (COPD) rehabilitation applications is to increase the functional capacity of the patients and improve the quality of life in daily living activities (ADL). Therefore, the investigators planned the study to determine the influence of ADL and related factors in severe COPD.

GOLD C and D COPD patients admitted to Bezmialem Vakif University Faculty of Health Sciences Department of Physiotherapy and Rehabilitation, Pulmonary Rehabilitation Application and Research Laboratory will be included in this study on a voluntary basis. Individuals who have experienced exacerbations of COPD in the last 6 weeks, have comorbidities affecting ambulation and have cognitive impairment will be excluded. Physical and sociodemographic characteristics of all participants will be recorded. Spirometric measurement will used to evaluate pulmonary functions, London Chest Activities Scale (LCADL) will used to evaluate daily living activities, six minute walking test (6MWT) will used to evaluate functional capacity, and mouth pressure will measured to evaluate respiratory muscle strength. (MIP: maximal inspiratory pressure, MEP: maximal expiratory pressure). Saint George Respiratory Questionnaire (SGRQ) for assessing quality of life, International Physical Activity Questionnaire (IPAQ) for assessing physical activity, COPD Assessment Test (CAT) for symptom assessment, and Hospital Anxiety and Depression Scale (HAD) for anxiety and depression assessment will be applied. SPSS 22.0 package program will be used in statistical analysis. For descriptive statistics, mean ± standard deviation values will be calculated and Pearson correlation test will be used in correlation analysis. p <0.05 will be the level of significance.

Enrollment

70 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Pulmonary function tests (PFT) value of FEV₁ / FVC <70%,
  • Being in GOLD III-IV groups,
  • Being over 18 years old,
  • Being able to read and to understand the spoken language.

Exclusion criteria

  • subjects have had COPD exacerbation in the last six weeks,
  • having comorbidities affecting ambulation and
  • cognitive disorders.

Trial design

70 participants in 1 patient group

Severe COPD patients
Description:
GOLD C and D group patients

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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