Chronic Obstructive Pulmonary Disease (COPD) Clinical Trials

Find Chronic Obstructive Pulmonary Disease (COPD) Clinical Trials Near You

Effects Of Low-Load Blood Flow Restriction Training Of The Upper Extremity In Patients With Chronic Obstructive Pulmonary Disease

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Chronic Obstructive Pulmonary Disease (COPD) is characterized by persistent airflow limitation, progressive dyspnea, and peripheral muscle dysfunction, significantly impairing functional capacity and quality of life. Although the combined implementation of aerobic and resistance exercises is recommended in pulmonary rehabilitation programs, early-onset ventilatory limitation in individuals with COPD often hinders tolerance to high exercise intensities. This limitation increases the need for alternative exercise approaches targeting peripheral muscle adaptations. Low-load blood flow restriction training (LL-BFRT), which enables improvements in muscle strength with low mechanical loads, has emerged as a potential option for this patient population. However, evidence regarding the effects of LL-BFRT in individuals with COPD-particularly on upper extremity muscles-remains limited. The aim of this study is to comparatively investigate the effects of LL-BFRT and sham-BFRT, both administered in addition to an aerobic exercise program in individuals diagnosed with stage II and III COPD, on upper extremity muscle strength, upper extremity functional capacity, activities of daily living performance, quality of life, functional exercise capacity, muscle oxygenation, and respiratory parameters. The study is designed as a randomized controlled, single-blind, quasi-experimental interventional trial. The expected outcomes are that LL-BFRT may enhance upper extremity muscle strength and functional capacity, improve activities of daily living and quality of life, and increase exercise tolerance due to its applicability at low mechanical loads. Furthermore, findings related to muscle oxygenation and respiratory parameters are anticipated to provide clinical evidence regarding the physiological effects of LL-BFRT on peripheral muscle adaptations. These results are expected to guide the integration of LL-BFRT as an alternative and safe approach in upper extremity exercise prescription within pulmonary rehabilitation programs, support clinical decision-making processes, and establish a scientific foundation for future research.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 40
Maximum Age: 80
Healthy Volunteers: f
View:

• Individuals aged 40-80 years with stage 2 and 3 COPD diagnosed according to GOLD criteria

‣ Clinically stable COPD (no exacerbation in the last 6 weeks)

⁃ Stable medical treatment for at least 4 weeks

⁃ No orthopedic or neurological problems that would prevent them from performing upper extremity exercises

⁃ Resting SpO2 ≥ 88%

⁃ Able to understand and follow verbal instructions in Turkish

⁃ Individuals with a Montreal Cognitive Assessment Scale (MoCa) score ≥ 24 will be included.

Locations
Other Locations
Turkey
Malatya Education and Research Hospital
RECRUITING
Malatya
Contact Information
Primary
Zeynal Yasacı, Doctor Lecturer
zeynal.yasaci@inonu.edu.tr
+905075409791
Backup
Emine Tonak
eminetonak4006@gmail.com
+905372994319
Time Frame
Start Date: 2026-02-15
Estimated Completion Date: 2026-12-25
Participants
Target number of participants: 36
Treatments
Experimental: Intervention Group
Participants will receive an 8-week upper extremity aerobic exercise program combined with low-load blood flow restriction training targeting upper extremity muscles.
Sham_comparator: Control Group
Participants will receive the same 8-week upper extremity aerobic exercise program combined with sham blood flow restriction training with non-therapeutic cuff pressure.
Sponsors
Leads: Inonu University

This content was sourced from clinicaltrials.gov