Skip to content

Music During Pulmonary Rehabilitation for Patients With COPD

Does Music During Pulmonary Rehabilitation in Individuals With Chronic Obstructive Pulmonary Disease (COPD) Improve Outcome? A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02980575
Enrollment
58
Registered
2016-12-02
Start date
2016-11-30
Completion date
2023-06-30
Last updated
2024-04-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Obstructive Pulmonary Disease

Keywords

COPD, Music, Exercise

Brief summary

This study is aimed at determining whether listening to music during exercise will improve health-related outcomes for individuals with chronic obstructive pulmonary disease (COPD). Half of the participants will listen to music while they exercise and half will not listen to music. The study will follow participants during their pulmonary rehabilitation program and for 6 months following completion of the program.

Detailed description

People with chronic obstructive pulmonary disease (COPD) are encouraged to undertake exercise training as part of their treatment. However, they often find themselves limited by breathlessness and tiredness in their legs. These barriers limit how much a person may benefit from an exercise program and how well they may keep up with a recommended schedule of exercise at home. One way of reducing feelings of breathlessness and leg tiredness is by listening to music during exercise. The impact of adding music to exercise versus exercise alone has not been explored in the setting of pulmonary rehabilitation. This study is aimed at determining the effect of listening to music during exercise sessions on exercise capacity, symptom severity, quality of life and motivation to exercise. People with COPD will be randomly allocated to exercise plus music or exercise alone. A music therapist will aid with music selection for the exercise plus music group and the music will be loaded onto a portable device that participants will listen to with earbuds. All participants will complete assessments before starting a pulmonary rehabilitation program, at the end of the 8-10 week program and 6 months following completion of the program. They will complete walking tests, report symptom severity and complete a series of questionnaires asking about their quality of life, symptoms and keenness to exercise.

Interventions

OTHERMusic
OTHERExercise

Sponsors

West Park Healthcare Centre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Medical diagnosis of COPD (physician diagnosis and spirometry with FEV1/FVC ratio \<70) and smoking history of greater than 10 pack years * Stable clinical state, with no acute exacerbations over the last 6 weeks * Referred to pulmonary rehabilitation program

Exclusion criteria

* Predominant diagnosis other than COPD (asthma, bronchiectasis, interstitial lung disease) * Co-morbidities (orthopaedic, neurological, cardiac) which might prevent safe exercise training * Substantial hearing difficulties (inability to hear music adequately) * Regularly uses music when exercising

Design outcomes

Primary

MeasureTime frameDescription
Change in end 6-minute walk test dyspnea and fatigue levelsChange from baseline to end of 8-week PR program or 6 month follow-upEnd test dyspnea and fatigue levels from best 6MWT
Multidimensional dyspnea profileChange from baseline to end of 8-week PR program or 6 months follow-up

Secondary

MeasureTime frame
Change in multidimensional fatigue inventory scoreChange from baseline to end of 8-week PR program or 6 month follow-up
Change in chronic respiratory disease questionnaire scoresChange from baseline to end of 8-week PR program or 6 month follow-up
Change in StepWatch physical acitvity monitor resultsChange from baseline to end of 8-week PR program or 6 month follow-up
Change in physical activity enjoyment scale scoreChange from baseline to end of 8-week PR program or 6 month follow-up
Change in hospital anxiety and depression scale scoreChange from baseline to end of 8-week PR program or 6 month follow-up

Countries

Australia, Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026