Effects of TPB-Based Cadence Exercise and Breathing Training on Physiological Parameters and Quality of Life in Patients With COPD
Condition(s) studied
Investigational drug(s) / intervention(s)
Breathing Training: A 12-week respiratory muscle training intervention based on the Theory of Planned Behavior. Participants will perform breathing training using an adjustable respiratory muscle training device according to a standardized training protocol. The intervention includes standardized instruction and training materials to support adherence.
Cadence Exercise: A 12-week cadence-guided walking exercise intervention based on the Theory of Planned Behavior. Participants will perform walking exercise using a metronome to guide the prescribed cadence according to a standardized training protocol. The intervention includes standardized instruction and training materials to support adherence.
Usual Care: Participants in this group will receive usual clinical care for chronic obstructive pulmonary disease according to routine clinical practice. No additional breathing training or cadence exercise intervention will be provided as part of the study.
Study summary
This randomized controlled trial aims to evaluate the effects of a Theory of Planned Behavior (TPB)-based intervention incorporating cadence exercise and breathing training on physiological parameters and quality of life in patients with chronic obstructive pulmonary disease (COPD). Eligible participants will be randomly assigned to receive breathing training, cadence exercise, a combined intervention of breathing training and cadence exercise, or usual care. The intervention will be conducted for 12 weeks, with assessments at baseline, Week 8, and Week 12. The study will evaluate changes in physiological parameters, exercise capacity, respiratory muscle strength, and quality of life. The findings may provide evidence for developing behavioral interventions to support pulmonary rehabilitation and improve health outcomes in people with COPD.
Eligibility
Primary outcome measure(s)
- Maximal Inspiratory Pressure (MIP) — Baseline (T0), Week 8 (T1), and Week 12 (T2)
Maximal inspiratory pressure (MIP) will be measured to evaluate respiratory muscle strength. - Maximal Expiratory Pressure (MEP) — Baseline (T0), Week 8 (T1), and Week 12 (T2)
Maximal expiratory pressure (MEP) will be measured to evaluate respiratory muscle strength. - Oxygen Saturation (SpO₂) — Baseline (T0), Week 8 (T1), and Week 12 (T2)
Oxygen saturation (SpO₂) will be measured to evaluate physiological status. - Six-Minute Walk Test (6MWT) — Baseline (T0), Week 8 (T1), and Week 12 (T2)
Six-minute walk test (6MWT) distance will be measured to evaluate exercise capacity. - COPD Assessment Test (CAT) — Baseline (T0), Week 8 (T1), and Week 12 (T2)
COPD Assessment Test (CAT) score will be used to assess the impact of COPD symptoms on patients' health status and quality of life. - Modified Medical Research Council Dyspnea Scale (mMRC) — Baseline (T0), Week 8 (T1), and Week 12 (T2)
Modified Medical Research Council Dyspnea Scale (mMRC) score will be used to assess the severity of dyspnea in patients with COPD. - St. George's Respiratory Questionnaire (SGRQ) — Baseline (T0), Week 8 (T1), and Week 12 (T2)
St. George's Respiratory Questionnaire (SGRQ) score will be used to assess health-related quality of life in patients with COPD. - WHOQOL-BREF (Taiwan Version) — Baseline (T0), Week 8 (T1), and Week 12 (T2)
WHOQOL-BREF (Taiwan Version) score will be used to assess health-related quality of life.
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Fu Jen Catholic University Hospital | New Taipei City | New Taipei City | Not Yet Recruiting |
| Taipei Hospital, Ministry of Health and Welfare | New Taipei City | New Taipei City | Recruiting |
More Fu Jen Catholic University Hospital trials in Taiwan
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07860008 on ClinicalTrials.gov ↗ ← All trials in Taiwan