Singing Intervention for Chronic Obstructive Pulmonary Disease (COPD)
EMPOWER
1 other identifier
interventional
5
1 country
1
Brief Summary
Why is this study being done? Chronic Obstructive Pulmonary Disease (COPD) causes airflow blockage creating breathing issues, distress, and lower well-being. COPD also causes hyperinflation of the lungs. The investigators are doing the study to learn more about improving lung function for patients with COPD by using voice-based experiences. What is being tested in this study? If singing/vocalizing can improve lung function. How long will I be in the study? The study will last 4 weeks and involve 2 in-person visits to KUMC with virtual vocal sessions two times a week over Zoom.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jul 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 25, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 26, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
November 26, 2024
CompletedFirst Submitted
Initial submission to the registry
April 13, 2026
CompletedFirst Posted
Study publicly available on registry
May 4, 2026
CompletedMay 4, 2026
April 1, 2026
4 months
April 13, 2026
April 28, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Quantitative Computed Tomography (qCT) Air Trapping
Functional Small Airways Disease Percent (range 0-100), indicating non-emphysematous air trapping percentage (fSAD) as lung volume percent of low attenuation areas below a radiodensity of -856 Hounsfield units (HU) on expiratory computed tomography (CT) and above -950HU on inspiratory CT. Higher values indicate greater air trapping and worse lung function.
Change from baseline after four weeks of the EMPOWER intervention
Secondary Outcomes (2)
Forced Expiratory Volume in 1 second (FEV1)
Change from baseline after four weeks of the EMPOWER intervention
Chronic Obstructive Pulmonary Disease (COPD) Assessment Test (CAT)
Change from baseline after four weeks of the EMPOWER intervention
Study Arms (1)
4-week singing intervention
EXPERIMENTALIndividual virtual singing sessions with a board-certified music therapist designed to target complete exhalation and reduce air trapping
Interventions
Using the Therapeutic Function of Music Plan, this individually tailored music therapy used singing and vocal exercises, guided by a board-certified music therapist, to aid in complete exhalation and reduce air trapping that occurs in chronic obstructive pulmonary disease (COPD).
Eligibility Criteria
You may qualify if:
- Participants 18 years of age or older
- Diagnosis of COPD
- Airflow obstruction and resting hyperinflation of the lung
- Able to hear within normal range with correction if needed
You may not qualify if:
- Pregnancy will be excluded for CT imaging safety and radiation safety
- Alpha-1 antitrypsin
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Kansas Medical Center
Kansas City, Kansas, 66160, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Rebecca J Lepping, PhD
University of Kansas Medical Center
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 13, 2026
First Posted
May 4, 2026
Study Start
July 25, 2024
Primary Completion
November 26, 2024
Study Completion
November 26, 2024
Last Updated
May 4, 2026
Record last verified: 2026-04