- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05832814
Music Therapy for COPD Rehabilitation (COPDMELODY)
The Effect of Music Therapy in Pulmonary Rehabilitation of COPD Patients Aged 40-75
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Physiology and psychology of COPD
COPD is a syndrome with a progressive pulmonary obstruction leading to increasingly impaired lung function due to chronic inflammation in the respiratory passages and pulmonary tissue. Living with COPD everyday life is a struggle and often marked with reduced physical activity, again leading to progression of disease, by which a vicious circle develops. Declining physical performance is associated with ventilation restriction, insufficient oxygen diffusion, respiratory muscle and peripheral skeletal muscle dysfunction, ventricular dysfunction and so on.
On a psychological level COPD patients tend to suffer from comorbidities such as increased stress and anxiety levels e.g. due to dyspnea and dysfunction. In conclusion, COPD often leads to a severe condition that both physically and psychologically can be very difficult to manage and cope with.
COPD and rehabilitation
Pulmonary rehabilitation (PR) is multidisciplinary and comprehensive intervention that may improve the interrelated physical and psychological consequences of the disease. It is designed to optimize functional status, reduce symptoms, improve health-related quality of life, reduce anxiety and depression, reduce exacerbations and mortality. However, in spite of documented efficacy and strong recommendations, PR is largely underutilized because most programs have been carried out on an inpatient or outpatient basis, relying on high cost, adequate doctors or therapists and regular visits to hospital. Another problem is the long-term maintenance of benefits once the hospital-based PR program has been completed, since gains achieved diminish progressively if training is abandoned. For these reasons, home-based PR has been proposed as an alternative to outpatient rehabilitation.
Just like the supervised training, a home-based PR program must include endurance exercise training, e.g. walking. Optimally, a program should also include respiratory muscle training.
Reviewing previous relevant researches, the current common home-based PR models have several limitations. The compliance is still pretty poor, both due to fear of dyspnea and fragility during training and tiring of inflexible exercise form. There is also a concern about ensurance of the exercise intensity during a home-based PR. Therefore it is of high importance to develop alternative rehabilitation activities that are motivating and are perceived helpful for the participants. This study aims to investigate music therapy(MT) as a new complementary therapy, since MT has the potential to facilitate exercise training and strengthen motivation of rehabilitation activity, with both physiological and psychological effects.
Music therapy and COPD rehabilitation
A number of international studies have investigated the effects of MT in relation to COPD patients. Music therapy targeting at COPD patients include offering music during exercise(distractive auditory stimulus therapy) and singing training. Compared with traditional aerobic exercise, rhythm-guided endurance training has the potential to help patients achieve a higher workload through decreasing or delaying the perception of exercise-induced dyspnea and fatigue. In terms of singing training, it could help patients learn how to control the respiratory function, including training and coordination of the related inspiratory and expiratory musculature. Moreover, from a psychology perspective, music in general seems to have an ability to promote motivations, and have a positive impact on well-being, anxiety and depression level.
Previous studies differ in methodology, and furthermore sample size and statistical power are not sufficient to conclude on significance and results. Most relevant researches are carried out in hospital or community-based face-to-face monitoring classes. No study has explored the integrated effects of music-facilitated exercise and singing training, although they might benefit COPD patients further through different physiological mechanisms compared with being applied separately. Therefore the present study is of high prevalence. Since it aims to develop alternative, motivating and personalized solutions to supplement standard PR, exploring whether singing training combined with melody-guided endurance exercise confers further benefits in exercise capacity and how music therapy influences patients' exercise performance, respiratory muscle strength, dyspnea, spirometry, quality of life and emotions.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Ting Yang, MD
- Phone Number: 84206272
- Email: zryyyangting@163.com
Study Locations
-
-
Beijing
-
Beijing, Beijing, China
- Recruiting
- China-Japan Friendship Hospital
-
Contact:
- Minghui Shi, MSc
- Email: sunflower_justdoit@163.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Participants with a clinical diagnosis of COPD and meeting the following criteria are eligible:
- Diagnosis of GOLD II-IV and without acute exacerbation within the last 4 weeks.
- Motivated for participating in the project (and acceptance of randomization)
- Sufficient mobility to attend PR
Exclusion Criteria:
- Certain comorbidities (e.g. unstable coronary complications)
- Severe cognitive disabilities (e.g. dementia)
- Inability to cope with the program because of severe hearing or visual disorder.
No previous singing experience or musical competence is required.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Integrated training
Rhythm-guided walking exercise coordinated with singing training as training activity in pulmonary rehabilitation: 12 weeks, three times a week for 1 hour, leading to a total of 36 sessions
|
For rhythm-guided walking exercise, the home exercise intensity, that is, the walking speed can be prescribed based on the incremental shuttle walking(ISWT) result.
A rhythm matching with the walking speed can be calculated.
Then patients will be provided a group of melodies identified by the calculated rhythm, which are also popular with the elder.
During exercise, the patients are required to walking on a fixed speed identical with the rhythm.
For singing training, patients follow the audios and videos to take training at home, which are recorded by singing teachers and physiotherapists prior to the trial.
Each session includes technical instructions in order to achieve better respiratory control during singing.
|
|
Experimental: Rhythm-guided exercise training
Rhythm-guided walking exercise as training activity in pulmonary rehabilitation: 12 weeks, three times a week for 1/2 hour, leading to a total of 36 sessions
|
For rhythm-guided walking exercise, the home exercise intensity, that is, the walking speed can be prescribed based on the incremental shuttle walking test(ISWT) result.
A rhythm matching with the walking speed can be calculated.
Then patients will be provided a group of melodies identified by the calculated rhythm, which are also popular with the elder.
During exercise, the patients are required to walking on a fixed speed identical with the rhythm.
|
|
No Intervention: Usual care
The usual care is the comparator in the trial, consisting of standard medical treatment and educational sessions including physical training, smoking cessation and vaccination.
And after the trial, the patients in this group will also be offered standard pulmonary rehabilitation according to the national guideline.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
incremental shuttle walking test(ISWT) distance
Time Frame: 12 weeks
|
incremental shuttle walking test distance
|
12 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Respiratory muscle strength
Time Frame: 12 weeks
|
maximum inspiratory pressure(MIP), maximum expiratory pressure(MEP)
|
12 weeks
|
|
Spirometry
Time Frame: 12 weeks
|
FEV1, FVC, FEV1/FVC, PEF, IC, RV, FRC, TLC
|
12 weeks
|
|
Short Physical Performance Battery(SPPB)
Time Frame: 12 weeks
|
Test for health-related physical performance
|
12 weeks
|
|
modified British medical research council(mMRC)
Time Frame: 12 weeks
|
It is a self-reported symptom questionnaire ranging from 0-4 score, higher scores mean a worse outcome.
|
12 weeks
|
|
COPD assessment test(CAT)
Time Frame: 12 weeks
|
It is a self-reported quality of life questionnaire ranging from 0-10 score, higher scores mean a worse outcome.
|
12 weeks
|
|
St. George's Respiratory Questionnaire (SGRQ)
Time Frame: 12 weeks
|
It is a self-reported symptom questionnaire ranging from 0-100 score, higher scores mean a worse outcome.
|
12 weeks
|
|
International Physical Activity Questionnaire Short Form (IPAQ-short)
Time Frame: 12 weeks
|
It is a questionnaire evaluating participants' quantity of physical activity in a recent week.
|
12 weeks
|
|
Hospital Anxiety and Depression Scale(HADS)
Time Frame: 12 weeks
|
It is a self-reported psychological status questionnaire ranging from 0-42 score, higher scores mean a worse outcome.
|
12 weeks
|
|
Compliance
Time Frame: 12 weeks
|
Self-produced sheet with registration each time of each participant's attendance or absence (with or without cause).
Registered continuously during intervention period.
|
12 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Minghui Shi, MSc, China-Japan Friendship Hospital
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2022-HX-16
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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