The effects of singing on lung function and quality of life for children and adults with cystic fibrosis

Irons JY, Kenny DT, Chang AB

Published Online:

May 12, 2010

Individuals with cystic fibrosis are at risk for respiratory infections due to too much mucus in their airways. Airway clearance is therefore an important part of cystic fibrosis management. Increasing anecdotal evidence suggests that singing may support lung function and enhance quality of life of people with cystic fibrosis. We searched for trials using the standard search module of the Cochrane Cystic Fibrosis and Genetic Disorders Group, as well as extensive searches in the relevant databases and publications. We did not find any randomised controlled trials that evaluated the benefits of singing in people with cystic fibrosis. The effects of singing in addition to standard therapy for people with cystic fibrosis remain unknown.

Abstract (click to read)

Background:

Cystic fibrosis is a genetically inherited, life-threatening condition that affects major organs. The management of cystic fibrosis involves a multi-faceted daily treatment regimen that includes airway clearance physiotherapy, taking pancreatic enzymes and other medications. Previous studies identified that compliance with this intensive treatment especially among adolescents with cystic fibrosis is poor. Because of both the nature and consequences of the illness and the relentless demands of treatments, many individuals with cystic fibrosis are likely to have a poor quality of life. Anecdotal evidence suggests that singing may provide rigorous exercises for the whole respiratory system as well as a means for emotional expression, which may enhance quality of life.

Objectives:

To evaluate the effects of a singing intervention in addition to usual therapy on the quality of life, morbidity, respiratory muscle strength and pulmonary function of children and adults with cystic fibrosis.

Search strategy:

We searched the Group's Cystic Fibrosis Trials Register, the Cochrane Central Register of Controlled Trials, major allied complementary data bases, and clinical trial registers. Hand searching for relevant conference proceedings and journals was also carried out.

Date of search of Trials Register: 02 September 2009.

Date of additional searches: 17 September 2009.

Selection criteria:

Randomised controlled trials in which singing (as an adjunctive intervention) is compared with either a sham intervention or no singing in people with cystic fibrosis.

Data collection and analysis:

No trials were found that met the selection criteria.

Main results:

No meta-analysis could be performed.

Authors' conclusions:

As no studies that met the criteria were found, this review is unable to support or refute the benefits of singing as a therapy for people with cystic fibrosis. Future randomised controlled trials are required to evaluate singing therapy for people with cystic fibrosis.

This record should be cited as:

Irons JY, Kenny DT, Chang AB. Singing for children and adults with cystic fibrosis. Cochrane Database of Systematic Reviews 2010, Issue 5. Art. No.: CD008036. DOI: 10.1002/14651858.CD008036.pub2

Assessed as up to date:

April 8, 2010

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Primary Review Group:

Cystic Fibrosis and Genetic Disorders Group

Health topics:

Genetic disorders > Cystic fibrosis > Physiotherapy & exercise

Lungs & airways > Cystic fibrosis > Physiotherapy & exercise

Complementary & alternative medicine > Genetic disorders > Cystic fibrosis

Complementary & alternative medicine > Lungs & airways > Cystic fibrosis

Cochrane Summaries^beta

Independent high-quality evidence for health care decision making

The effects of singing on lung function and quality of life for children and adults with cystic fibrosis

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