ClinicalTrials.Veeva

Menu

Exploring the Effects of Aerobic Exercise Combined with BFRT on Patients with COPD

N

National Cheng Kung University

Status

Enrolling

Conditions

Chronic Obstructive Pulmonary Disease

Treatments

Behavioral: Aerobic exercise intervention
Behavioral: Blood flow restriction (BFR) intervention
Behavioral: Disease and exercise suggestion

Study type

Interventional

Funder types

Other

Identifiers

NCT06756646
B-ER-113-298

Details and patient eligibility

About

Investigate the effects of exercise training on the cardiopulmonary function and exercise capacity in COPD patients.

Full description

The systemic effects of Chronic Obstructive Pulmonary Disease (COPD) can precipitate a series of complications, including cardiovascular disorders, muscle atrophy, and osteoporosis. These comorbid conditions often result in decreased physical activity and suboptimal physical fitness, compelling patients to lead a sedentary lifestyle to mitigate exercise-induced dyspnea. Addressing the limitations in exercise tolerance remains a critical therapeutic goal in the treatment of COPD. According to research, exercise intolerance is caused by both poor pulmonary function and associated skeletal muscle dysfunction. Blood flow restriction training, a new rehabilitation technique, has shown promise in improving muscular strength at lower exercise intensities and in shorter timeframes, presenting a fresh approach to COPD rehabilitation.

The research aims to investigate the impact of incorporating blood flow restriction training into a holistic aerobic exercise program on exercise capacity and quality of life among patients with COPD. The findings are intended to clarify the potential of this innovative training technique as a supplementary therapeutic strategy in the management of COPD.

Enrollment

90 estimated patients

Sex

All

Ages

30 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. COPD classified as levels 2-4.
  2. Stable condition without worsening in the past three months.
  3. No participation in any rehabilitation program within the past six months.
  4. Ability to understand and follow verbal commands and cooperate with an exercise training program.

Exclusion criteria

  1. Unconscious or unable to cooperate with the evaluator.
  2. Hospitalization due to acute illness within the past three months.
  3. Severe joint diseases or history of lower limb surgery.
  4. Severe cardiovascular disease (e.g., presence of a cardiac pacemaker or acute myocardial infarction within the past six months).
  5. Dependence on oxygen supply.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

90 participants in 3 patient groups

Usual care group
Active Comparator group
Description:
The Usual care group will receive COPD and exercise-related education.
Treatment:
Behavioral: Disease and exercise suggestion
Aerobic exercise group-cycling
Experimental group
Description:
The aerobic exercise group will receive cycling training intervention 2-3 times per week for 2 months.
Treatment:
Behavioral: Aerobic exercise intervention
BFR group-cycling + BFR
Experimental group
Description:
The BFR group will receive cycling training combined with BFR intervention 2-3 times per week for 2 months.
Treatment:
Behavioral: Blood flow restriction (BFR) intervention

Trial contacts and locations

1

Loading...

Central trial contact

Kun-Ling Tsai, Ph.D.; Yu-Ting Huang, M.S.

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems