Effect of singing lessons on breathlessness in patients with chronic obstructive pulmonary disease (COPD)

ISRCTN ISRCTN17544114
DOI https://doi.org/10.1186/ISRCTN17544114
Protocol serial number cro870 protocol version 2
Sponsor Imperial College London (UK)
Funder Royal Brompton & Harefield Arts (rb&h Arts), Royal Brompton Hospital (UK)
Submission date
16/01/2009
Registration date
19/02/2009
Last edited
11/12/2014
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Respiratory
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data

Plain English summary of protocol

Not provided at time of registration

Contact information

Dr Nicholas Hopkinson
Scientific

Royal Brompton Hospital
Fulham Road
London
SW3 6NP
United Kingdom

Study information

Primary study designInterventional
Study designRandomised controlled single-blind trial
Secondary study designRandomised controlled trial
Study type Participant information sheet
Scientific titleEffect of singing lessons on breathlessness in patients with chronic obstructive pulmonary disease (COPD): a randomised controlled single-blind trial
Study acronymESLBPC
Study objectivesThat a course of singing lessons will improve breathlessness in patients with chronic obstructive pulmonary disease (COPD).
Ethics approval(s)Brompton, Harefield and National Heart and Lung Institute (NHLI) REC, approved on 11/10/2007 (ref: 07/H0708/90)
Health condition(s) or problem(s) studiedChronic obstructive pulmonary disease (COPD)
InterventionParticipants will be randomly allocate to the following two arms:
Intervention group: A 6-week course of singing lessons (1 hour/ lesson) twice weekly
Control group: Standard care only
Intervention typeOther
Primary outcome measure(s)

Single breath counting and breath hold time.

All primary and secondary outcomes will be assessed at 7 weeks.

Key secondary outcome measure(s)

1. Quality of life (QOL): St George's Respiratory Questionnaire (SGRQ), Transition Dyspnoea Index, SF-36® Health Survey
2. Shuttle walking test (SWT)

All primary and secondary outcomes will be assessed at 7 weeks.

Completion date01/08/2009

Eligibility

Participant type(s)Patient
Age groupOther
SexAll
Target sample size at registration64
Key inclusion criteria1. Both males and females, no age limits
2. COPD patients able to comply with a course of lessons
3. Medical Research Council (MRC) dyspnoea score >3/5
Key exclusion criteriaUnable to comply with course
Date of first enrolment22/01/2009
Date of final enrolment01/08/2009

Locations

Countries of recruitment

  • United Kingdom
  • England

Study participating centre

Royal Brompton Hospital
London
SW3 6NP
United Kingdom

Results and Publications

Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
IPD sharing plan

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Results article results 03/08/2010 Yes No
Abstract results 18/05/2010 No No
Participant information sheet Participant information sheet 11/11/2025 11/11/2025 No Yes