NCT07563283

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
5

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jul 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 25, 2024

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 26, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 26, 2024

Completed
1.4 years until next milestone

First Submitted

Initial submission to the registry

April 13, 2026

Completed
21 days until next milestone

First Posted

Study publicly available on registry

May 4, 2026

Completed
Last Updated

May 4, 2026

Status Verified

April 1, 2026

Enrollment Period

4 months

First QC Date

April 13, 2026

Last Update Submit

April 28, 2026

Conditions

Keywords

musicsingingsmall airways disease

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

EXPERIMENTAL

Individual virtual singing sessions with a board-certified music therapist designed to target complete exhalation and reduce air trapping

Behavioral: singing intervention for COPD

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).

Also known as: Engaging Music for Pulmonary Obstruction With Expiratory Restoration (EMPOWER)
4-week singing intervention

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Pulmonary Disease, Chronic Obstructive

Condition Hierarchy (Ancestors)

Lung Diseases, ObstructiveLung DiseasesRespiratory Tract DiseasesChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Rebecca J Lepping, PhD

    University of Kansas Medical Center

    PRINCIPAL INVESTIGATOR

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

Locations