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Combining Manual Soft Tissue Release and Exercise Training in COPD: the Effect on LF, EC, and CAF

N

National Cheng Kung University

Status

Completed

Conditions

Exercise Training
Cardiac Autonomic Function
Manual Soft Tissue Release
Chronic Obstructive Pulmonary Disease
Exercise Capacity
Lung Function

Treatments

Behavioral: Manual soft tissue release
Behavioral: Exercise training
Behavioral: Myofascial release

Study type

Interventional

Funder types

Other

Identifiers

NCT06389734
B-ER-111-470

Details and patient eligibility

About

The potential effects of combining manual soft tissue release and physical exercise training on lung function, exercise capacity, and cardiac autonomic function in patients with moderate and severe chronic obstructive pulmonary disease were investigated.

Full description

Chronic obstructive pulmonary disease (COPD) commonly presents with accessory respiratory muscle tightness and weakness, affecting chest wall compliance and lung elasticity. However, traditional physical therapy interventions, including pursed-lip breathing, sputum clearance techniques, and respiratory muscle training, are often used in treatment guidelines, with few studies focusing on muscle release for the accessory respiratory muscles. Although the effects of manual therapy on lung function and chest tightness in COPD have been demonstrated, the effects of soft tissue release combined with exercise intervention on COPD, including lung function, exercise capacity, and cardiac autonomic function, remain unknown. Therefore, this study proposes a randomized controlled trial to investigate the effects of manual soft tissue release combined with exercise training on lung function, exercise capacity, and cardiac autonomic function in patients with COPD. It is expected that the results of this study will demonstrate that combining manual soft tissue release with exercise training may increase gas exchange in the lungs, reduce respiratory effort, improve co-morbidities, delay disease progression, and enhance patient quality of life and clinical intervention.

Enrollment

70 patients

Sex

All

Ages

30 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • GOLD grade II~IV
  • Stable condition
  • No acute exacerbations in 6 weeks

Exclusion criteria

  • Acute heart failure and, or arrhythmia
  • Pulmonary arterial hypertension
  • Skeletal and, or neuromuscular disorders
  • Chest surgery
  • Untreated or uncontrolled conditions
  • Rheumatoid conditions
  • Depends on oxygen supply

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

70 participants in 2 patient groups

Intervention group
Experimental group
Description:
The intervention group will receive combining manual soft tissue release and exercise training.
Treatment:
Behavioral: Manual soft tissue release
Behavioral: Exercise training
Control group
Active Comparator group
Description:
The control group will receive combining myofascial release and exercise training.
Treatment:
Behavioral: Exercise training
Behavioral: Myofascial release

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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