Chronic Obstructive Pulmonary Disease (COPD) Clinical Trials

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Comparison of Respiratory and Peripheral Muscle Strength, Exercise Capacity, and Muscle Oxygenation in Individuals With COPD and PRISM

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

COPD is a preventable and treatable lung disease characterized by persistent and progressive airflow limitation. PRISm, on the other hand, is a spirometry pattern that does not meet COPD diagnostic criteria despite symptoms and functional impairments, but requires maintenance. PRISm can predispose to the development of COPD and exacerbations, and can reduce exercise capacity by reducing respiratory function and oxygen consumption. There are no studies in the literature comparing respiratory muscle strength, peripheral muscle strength, and oxygenation in PRISm, COPD, and healthy individuals. Therefore, this study aimed to evaluate these parameters and compare them with healthy individuals.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 40
Healthy Volunteers: t
View:

⁃ For the COPD group:

• Being \>40 years old,

• Being diagnosed with COPD,

• Being clinically stable,

• Volunteering to participate in the study.

⁃ For the PRISm group:

• Being \>40 years old,

• Being diagnosed with PRISm,

• Volunteering to participate in the study.

⁃ For the healthy control group:

• Being \>40 years old,

• Volunteering to participate in the study.

Locations
Other Locations
Turkey
Karabuk University, Physiotherapy and Rehabilitation Application and Research Center
RECRUITING
Karabük
Contact Information
Primary
Musa Güneş, PhD
musagunes52@hotmail.com
03704789081
Time Frame
Start Date: 2025-10-05
Estimated Completion Date: 2026-11-30
Participants
Target number of participants: 60
Treatments
Patients with COPD
Patients with chronic obstructive pulmonary disease will be included.
Patients with PRISm
Patients with preserved ratio impaired spirometry will be included.
Control
Healthy controls will be included.
Sponsors
Leads: Karabuk University

This content was sourced from clinicaltrials.gov