Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
100 participants
INTERVENTIONAL
2019-04-01
2020-04-30
Brief Summary
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Detailed Description
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Approximately 440,000 Irish people suffer from Chronic Obstructive Pulmonary Disease (COPD) (Health Service Executive (HSE), 2018) and it is the fourth most common cause of death, after lung cancer, heart disease and stroke. In addition to many physical issues, patients lack the physical endurance or confidence to participate fully in their lives, leading to isolation, social exclusion and co-morbid depression and anxiety. Addressing the management of people with COPD was highlighted as an urgent priority in the Government's 2017 National Healthcare Quality Reporting System annual report. This application proposes a community-based singing intervention replicating that successfully delivered by the British Lung Foundation (BLF) (https://www.blf.org.uk/support-for-you/singing-for-lung-health). This project is unique in Ireland, and builds on established ties between the (Principal Investigator) PI and the local COPD community. It is supported by COPD Support Ireland.
Study design:
* This study is a pre-post intervention study involving a cohort of COPD patients who are members of regional COPD support groups in Limerick, Ennis and Nenagh.
* Pre-intervention testing will involve self-reported measures wellness using standardised tools as well as a walking test (6-minute walking test (6MWT) and spirometry to asses lung function.
* The intervention is an eight-week singing intervention led by an experienced singing instructor who will be provided with relevant training on singing with lung impairment. Participants will also be provided with a compact disk (CD) for between intervention practice at their own discretion.
* Post-intervention testing will repeat tests done at baseline. Testing will be carried out in both instances by the PI and clinical staff from the geographical area.
Focus groups will be conducted with a sample from each group to support a qualitative evaluation of the intervention.
Participants:
Approximately 30 participants from each region will be invited to participate. Participants must have a diagnosis of COPD, must be clinically stable, and not have suffered an exacerbation in the 2 weeks prior to testing.
Participants have been sourced through the clinicians involved in this study, and the teaching contacts of the PI.
Procedures/Methods :
Planing stage: April/May 2019
* Community singing leader will attend United Kingdom (UK) training course delivered by BLF "Singing for Lung Health" leaders. - Liaise with three regional COPD patient groups (Limerick, Ennis, Nenagh) to gather informed consent, and finalise intervention details.
* Design and record CD featuring exercises and songs for home practice for participants. These will be provided freely to participants and based on song preference of patient-partners, and informed by disease limiting factors.
* Baseline testing of participants as discussed will take place in a community setting where the groups normally meet for other exercise and social activities.
Intervention stage: June/July 2019
* The intervention will comprise eight weekly one-hour singing sessions. Sessions will be comprised of physical warm-ups, breathing exercises, and vocal exercises such as rhythm and pitch games.
* The intervention will be delivered by the community singing leader and the PI will attend the first session to explain the clinical relevance of exercises.
Conditions
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Study Design
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NA
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
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Group singing and breathing control training
Singstrong:
Group singing and breathing control training
Interventions
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Singstrong:
Group singing and breathing control training
Eligibility Criteria
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Inclusion Criteria
* All participants must be at least 18 years of age. There is no upper age limit.
* Participants may be male or female.
* They must have a good command of written and spoken English.
Exclusion Criteria
* Presence of physical of psychological co-morbidities precluding participation in either testing or intervention.
18 Years
ALL
No
Sponsors
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Irish Research Council
OTHER
University of Limerick
OTHER
Responsible Party
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Principal Investigators
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Roisin Cahalan, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Limerick
Locations
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University of Limerick
Limerick, , Ireland
Countries
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Other Identifiers
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NF1
Identifier Type: -
Identifier Source: org_study_id
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