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The Effects of Singing Training for Patients With Chronic Obstructive Pulmonary Disease (COPD)

Primary Purpose

Chronic Obstructive Pulmonary Disease

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Singing training
Physical Training
Sponsored by
University of Aarhus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Chronic Obstructive Pulmonary Disease focused on measuring COPD, Chronic Obstructive Pulmonary Disease, Randomised controlled trial (RCT), Rehabilitation, Singing Training

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Participants with a clinical diagnosis of COPD and who meet the following criteria are eligible:

  1. Recommended for Pulmonary Rehabilitation and minimum mMRC2 level of dyspnea
  2. Motivated for participating in the project (and acceptance of randomization)
  3. Sufficient mobility to attend PR

Exclusion Criteria:

  1. Certain comorbidities (e.g. unstable coronary complications)
  2. Severe cognitive disabilities (e.g. dementia)
  3. Inability to speak or understand Danish

No previous singing experience or musical competence is required.

Sites / Locations

  • Rudersdal Health Centre
  • Fakse Health Centre
  • Vesthimmerland Health Centre
  • Hedensted Health Centre
  • Helsingor Health Centre
  • Ikast-Brande Health Centre
  • Lemvig Health Centre
  • Lolland Health Centre
  • Silkeborg Health Centre
  • Slagelse Health Centre
  • Vordingborg Health Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Singing Training

Physical Training

Arm Description

Singing Training as training activity in Pulmonary Rehabilitation: 10 weeks, twice a week for 1 1/2 hour, leading to a total of 20 sessions.

Physical Training as training activity in Pulmonary Rehabilitation: 10 weeks, twice a week for 1 1/2 hour, leading to a total of 20 sessions.

Outcomes

Primary Outcome Measures

6 Minutes Walk Distance (6MWD)
Meters

Secondary Outcome Measures

Pedometer
Number of steps (worn for 1 week (7 days) at baseline and post intervention)
St. George's Respiratory Questionnaire (SGRQ)
Quality of Life-questionnaire (self-reported)
Forced Expiratory Volume Predicted (FEV1%)
The FEV1% is the FEV1 divided by the FVC (Forced Vital Capacity) times 100: FEV1%=FEV1/VC X100
Breath Hold Test
Number of seconds (from max inspiration)
Single-breath Count
Numbers counted (beats per minute=60) (from max inspiration)
Compliance
Self-produced excel sheet with registration each time of each participant's attendance or absence (with or without cause). Registered continuously during intervention period.
Musical Ear Test (MET)
Test for musical competence: 104 trials on which participants judge whether two short musical phrases (melody/rhythm) are identical or not

Full Information

First Posted
September 1, 2017
Last Updated
June 20, 2023
Sponsor
University of Aarhus
Collaborators
Region Zealand
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1. Study Identification

Unique Protocol Identification Number
NCT03280355
Brief Title
The Effects of Singing Training for Patients With Chronic Obstructive Pulmonary Disease (COPD)
Official Title
The Effects of Singing Training for Patients With Chronic Obstructive Pulmonary Disease (COPD)
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
August 1, 2017 (Actual)
Primary Completion Date
April 15, 2019 (Actual)
Study Completion Date
April 15, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Aarhus
Collaborators
Region Zealand

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Patients with Chronic Obstructive Pulmonary Disease (COPD) experience physiological and psychological complications, such as shortness of breath, anxiety and depression. This has negative influence on their social life, daily activity level and overall quality of life. Patients can participate in a pulmonary rehabilitation program (PR) for the purpose of better managing of the disease and its symptoms and for avoiding future relapses and hospitalisations. However there is a large number of dropouts from PR, and therefore a need for investigation of new activities. Singing training may be one such potential relevant and motivating rehabilitation activity. This study aims to investigate the effects of singing training on both physiological and psychological aspects, and will compare the effects with that of physical training (golden standard in PR). Effects will be investigated in a randomised controlled trial (RCT) with 10 week intervention period. In all the study includes 11 municipalities from around all regions of Denmark, and in all 220 participants.
Detailed Description
The number of patients with Chronic Obstructive Pulmonary Disease (COPD) is is rapidly increasing, and the disease is projected to be the third leading cause of death worldwide in 2020. At the present time 320.000 people in Denmark suffer from COPD, though only half of them are diagnosed and hence treated with appropriate medication. Often patients are not diagnosed until the pulmonary function is only 50% and therefore at a severe stage of the disease, where there tends to be a high rate in hospitalisations and recurring exacerbations with increasing symptoms. COPD amounts to 10% of the Danish national health care budget, and Denmark has the highest COPD related mortality rate in the EU. Besides sufficient medical treatment, patients are offered attendance in pulmonary rehabilitation, since lifestyle changes are crucial in order to prevent disease progression, and for better management of symptoms and higher Quality of Life (QoL). Pulmonary rehabilitation consists of evidence based activities and are based on international and national guidelines. However there is a need for investigation of new motivating and perceived relevant rehabilitation activities due to a large number of drop-outs of the ordinary rehabilitation program. The study aims to examine the effects of singing training for patients with COPD in relation to physiological as well as psychological aspects. Intervention is singing training, and active control is usual care: Physical training (golden standard and standard part of ordinary pulmonary rehabilitation). HYPOTHESES: The main hypothesis of this study is that singing training as activity in pulmonary rehabilitation is non-inferior in relation to effects on specific physiological and specific psychological/psychosocial aspects compared to physical training (control group). More specifically, the hypotheses are: Singing training leads to a positive rehabilitation process as regards selected physiological parameters as well as selected psychological and psychosocial parameters. Attending the singing training program leads to a more consistent rehabilitation process with higher motivation and less drop outs among the participants than in the control group. Potential moderators and mediators: During the project potential mediating and moderating factors will be explored, e.g. including socio-demographic, disease-, lifestyle- and attitude-related characteristics (COPD participants are e.g. characterised by relatively old age and lower socio-economic status). Furthermore, relevant psychological aspects (e.g. in correlation with building and maintaining motivation) will be investigated. Also baseline attitude towards singing (and physical training), the relationship between the facilitator and participants, and the significance of influence associated with the intervention (e.g. in terms of musical taste) will be taken into consideration. BACKGROUND: Physical and psychological effects 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 by continuous dyspnea, cough and sputum. The patients often suffer from emphysema leading to stiff lungs and insufficient diffusion of oxygen. This again leads to a vicious circle with lack of control of respiratory function, increased hyperinflation and forced, clavicular oriented breathing. Comorbidities such as heart disease, muscle wasting, hypertension and infections are common, which again lead to further complications. On a psychological level patients are often also affected negatively as a sequela of the disease. E.g. COPD patients tend to suffer from comorbidities such as increased stress and anxiety levels e.g. due to dyspnea. Furthermore patients experience social isolation, financial downfall and generally impaired Quality of Life (QoL). Also activities of daily life are significantly affected by COPD, and the reduced activity again leads to depression and further physical health problems, by which a vicious circle develops. In other words COPD often leads to a severe condition that both physically and psychologically can be very difficult to manage and cope with. COPD and rehabilitation: Although the COPD related degeneration of the lungs is irreversible, treatment may slow down further progression, and improve the interrelated physical and psychological consequences of the disease. Besides required medical treatment participants life style change, e.g. smoking cessation, physical training and psychosocial support, are crucial. According to guidelines from the Danish Government Health Agency patients are encouraged to join an 8-12-wk multidisciplinary rehabilitation program in order to improve physical and mental condition, improve general function and QoL levels, and prevent exacerbations, hospitalisations and early mortality. The overall recommendations are that patients should not only receive clinical control and medical treatment, but should also participate in additional interventions. This is essential in terms of supporting the participants in maintaining (or retrieve) empowerment and self-dependence, also as regards education, work, income, housing and social network. However, there is a high drop out rate, both due to exacerbations or mortality and to lack of mobility or motivation. Therefore it is of high importance to develop alternative rehabilitation activities that are motivating and are perceived relevant for the participants and that both includes physical training and enables the participants to lead their lives with a higher QoL level. Furthermore, physical and psychological effects of COPD seem to influence each other significantly, suggesting that both areas should be considered in rehabilitation of COPD patients. There is an unmet need for new types of interventional therapies to help COPD patients. This study aims to investigate singing training as a potential new rehabilitation activity, since singing might lead to a more efficient utilisation of the remaining respiratory function of participants with COPD and improve QoL. Singing and COPD rehabilitation: A number of international studies have investigated the effects of singing in relation to COPD patients. The core of singing activity is to learn how to control the respiratory function, including training and coordination of both inspiration and expiration function, focusing on the related primary and secondary musculature. An essential part of the singing training is also focused exercises for posture, relaxation and general body awareness. Moreover, group singing might have a positive impact on the experiences of social interaction, and music in general seems to have an ability to create emotions, and seems to have a positive impact on well-being, anxiety and depression level. Previous studies differ in methodology (randomized controlled trials, observational studies, qualitative studies and literature reviews), and furthermore sample size and statistical power are not sufficient to conclude on significance and results. Therefore it is of great importance to conduct further and larger trials in order to provide evidence to the field. In Denmark a number of COPD choirs have been launched, and it seems to have become common-sense that singing is healthy to patients with COPD. The choirs however are launched quite randomly, there is no common methodology on the COPD choirs, and also effects of the choir singing has not yet been investigated. COPD singing therefore has not yet been considered in the national guidelines as a validated rehabilitation activity, however popular among the participants. Therefore the present study is of high relevance, since it aims to provide knowledge and evidence within this field, for the benefit of the large and dramatically growing number of COPD patients. METHODS: Study design: The study is a non-pharmacological two-armed randomized controlled trial with intervention group receiving singing training (ST), and active control group receiving "golden standard": Physical training (PT). Both groups will participate in a 10 weeks' program, 1 1/2 hour, twice a week. Both groups also participate in education activities as part of pulmonary rehabilitation, such as smoking cessation course. Participants randomised to singing training will be offered opportunity to participate in standard physical training post intervention.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease
Keywords
COPD, Chronic Obstructive Pulmonary Disease, Randomised controlled trial (RCT), Rehabilitation, Singing Training

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Non-pharmacological, intervention based, group randomised (cluster randomised) controlled trial, 2 arms (intervention and active control group)
Masking
InvestigatorOutcomes Assessor
Masking Description
Assessor (nurse) is masked, primary investigator is masked
Allocation
Randomized
Enrollment
270 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Singing Training
Arm Type
Experimental
Arm Description
Singing Training as training activity in Pulmonary Rehabilitation: 10 weeks, twice a week for 1 1/2 hour, leading to a total of 20 sessions.
Arm Title
Physical Training
Arm Type
Active Comparator
Arm Description
Physical Training as training activity in Pulmonary Rehabilitation: 10 weeks, twice a week for 1 1/2 hour, leading to a total of 20 sessions.
Intervention Type
Behavioral
Intervention Name(s)
Singing training
Intervention Description
Each session will contain technical instruction in order to achieve better respiratory control and primary muscular strength, and with focus on techniques for efficient expiration. Sessions will also focus on musical content and interpretation as well as interaction, the social aspects and joy of singing together. Prior to the trial all singing teachers will participate in a 2 days' workshop, where they will be instructed in sufficient methodology and didactics, and will obtain profound knowledge about the disease pathology and related physiology.
Intervention Type
Behavioral
Intervention Name(s)
Physical Training
Intervention Description
Physical Training (golden standard training activity in pulmonary rehabilitation) - usual care - is the active comparator in the trial. The programme is based on the national guidelines for pulmonary rehabilitation, and consists of supervised warm-ups, aerobic exercises, workout (strength), and breathing exercises. Physical Training is conducted by the local physiotherapists in the local health centres.
Primary Outcome Measure Information:
Title
6 Minutes Walk Distance (6MWD)
Description
Meters
Time Frame
12 weeks (+/- 2 weeks)
Secondary Outcome Measure Information:
Title
Pedometer
Description
Number of steps (worn for 1 week (7 days) at baseline and post intervention)
Time Frame
12 weeks (+/- 2 weeks)
Title
St. George's Respiratory Questionnaire (SGRQ)
Description
Quality of Life-questionnaire (self-reported)
Time Frame
12 weeks (+/- 2 weeks)
Title
Forced Expiratory Volume Predicted (FEV1%)
Description
The FEV1% is the FEV1 divided by the FVC (Forced Vital Capacity) times 100: FEV1%=FEV1/VC X100
Time Frame
12 weeks (+/- 2 weeks)
Title
Breath Hold Test
Description
Number of seconds (from max inspiration)
Time Frame
12 weeks (+/- 2 weeks)
Title
Single-breath Count
Description
Numbers counted (beats per minute=60) (from max inspiration)
Time Frame
12 weeks (+/- 2 weeks)
Title
Compliance
Description
Self-produced excel sheet with registration each time of each participant's attendance or absence (with or without cause). Registered continuously during intervention period.
Time Frame
10 weeks
Title
Musical Ear Test (MET)
Description
Test for musical competence: 104 trials on which participants judge whether two short musical phrases (melody/rhythm) are identical or not
Time Frame
12 weeks (+/- 2 weeks)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Participants with a clinical diagnosis of COPD and who meet the following criteria are eligible: Recommended for Pulmonary Rehabilitation and minimum mMRC2 level of dyspnea 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 speak or understand Danish No previous singing experience or musical competence is required.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Uffe Bodtger, MD PhD
Organizational Affiliation
Region Zealand
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Peter Vuust, Professor
Organizational Affiliation
Aarhus Univeristy
Official's Role
Study Director
Facility Information:
Facility Name
Rudersdal Health Centre
City
Birkerod
ZIP/Postal Code
3460
Country
Denmark
Facility Name
Fakse Health Centre
City
Fakse
ZIP/Postal Code
4640
Country
Denmark
Facility Name
Vesthimmerland Health Centre
City
Farso
ZIP/Postal Code
9640
Country
Denmark
Facility Name
Hedensted Health Centre
City
Hedensted
ZIP/Postal Code
8722
Country
Denmark
Facility Name
Helsingor Health Centre
City
Helsingor
ZIP/Postal Code
3000
Country
Denmark
Facility Name
Ikast-Brande Health Centre
City
Ikast
ZIP/Postal Code
7430
Country
Denmark
Facility Name
Lemvig Health Centre
City
Lemvig
ZIP/Postal Code
7620
Country
Denmark
Facility Name
Lolland Health Centre
City
Maribo
ZIP/Postal Code
4930
Country
Denmark
Facility Name
Silkeborg Health Centre
City
Silkeborg
ZIP/Postal Code
8600
Country
Denmark
Facility Name
Slagelse Health Centre
City
Slagelse
ZIP/Postal Code
4200
Country
Denmark
Facility Name
Vordingborg Health Centre
City
Vordingborg
ZIP/Postal Code
4760
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34625480
Citation
Kaasgaard M, Rasmussen DB, Andreasson KH, Hilberg O, Lokke A, Vuust P, Bodtger U. Use of Singing for Lung Health as an alternative training modality within pulmonary rehabilitation for COPD: a randomised controlled trial. Eur Respir J. 2022 May 19;59(5):2101142. doi: 10.1183/13993003.01142-2021. Print 2022 May.
Results Reference
derived
PubMed Identifier
33257493
Citation
Kaasgaard M, Andersen IC, Rasmussen DB, Hilberg O, Lokke A, Vuust P, Bodtger U. Heterogeneity in Danish lung choirs and their singing leaders: delivery, approach, and experiences: a survey-based study. BMJ Open. 2020 Nov 30;10(11):e041700. doi: 10.1136/bmjopen-2020-041700.
Results Reference
derived

Learn more about this trial

The Effects of Singing Training for Patients With Chronic Obstructive Pulmonary Disease (COPD)

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