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Music Therapy to Address Patients' Journeys With Chronic Illness, Outcomes, and Readmission

Music Therapy to Address Patients' Journeys With Chronic Illness, Outcomes, and Readmission

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06214325
Acronym
MAJOR CHORD
Enrollment
20
Registered
2024-01-19
Start date
2024-01-15
Completion date
2024-06-11
Last updated
2024-08-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Obstructive Pulmonary Disease, Heart Failure

Keywords

Music Therapy, Chronic Obstructive Pulmonary Disease, Heart Failure, In-person, Virtual

Brief summary

Conduct a pilot study (n = 20) to explore the feasibility and acceptability of the MAJOR CHORD music therapy (MT) intervention (i.e., two in-person MT sessions prior to discharge and two virtual MT sessions post-discharge) and collection of patient-reported outcomes through 30 days after hospital discharge. The investigators will uncover any potential modifications that need to be made to the intervention and data collection process prior to initiating the randomized trial.

Interventions

BEHAVIORALMusic Therapy

Board-certified music therapists (i.e., MT-BC credential) will provide two music therapy sessions, a minimum of 24 hours apart, that include education and disease-specific content (e.g., harmonica exercises for respiratory health \[COPD\] or music-based breathing exercises \[HF\]) prior to patients' discharge and two virtual music therapy sessions that address music-assisted relaxation and imagery, additional techniques for managing psychosocial stressors, and gratitude exercises post-discharge.

Sponsors

Kulas Foundation
CollaboratorOTHER
University Hospitals Cleveland Medical Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 89 Years
Healthy volunteers
No

Inclusion criteria

* Age range: ≥40 to ≤89 years * Hospitalized at UH Cleveland Medical Center (UHCMC) with anticipated length of stay following recruitment ≥ 2 days as documented in electronic health record (EHR) * Diagnosed (i.e., ICD-10 code within the EHR) with either COPD (J44) or HF (I50) with confirmed ICD-10 code in EHR * Able to read and understand English * Screening positive for depression and/or anxiety as evidenced by: GAD-7 anxiety score ≥ 10 and PHQ-9 depression score ≥ 10 * Access to WiFi, active email address & laptop, tablet, and/or PC with videoconferencing capabilities * Has reliable support person who can be available to respond in case of a medical emergency at any time * Has reliable access to a mobile device with active data plan

Exclusion criteria

* Significant hearing and/or visual impairment as documented in EHR * Unable to independently provide consent (i.e., no proxy consent) * Active suicidal ideation documented in inpatient psychiatry note during current hospital admission or expressed at any point verbally or in writing to study staff * Severe psychological comorbidity (e.g., psychosis, schizophrenia) that would prevent patient from engaging fully in intervention as documented in EHR * Currently admitted to intensive care unit * Receiving active cancer treatment (e.g., chemotherapy, radiation, immunotherapy) as documented in EHR * Diagnosed with medical condition likely to be terminal within 24 weeks as documented in EHR * On wait list for heart transplantation or ventricular assist device (VAD) as documented in EHR * NYHA Stage IV HF or end-stage COPD as documented in EHR * Receiving hospice care as documented in EHR * Active substance abuse as documented in EHR

Design outcomes

Primary

MeasureTime frameDescription
Comparison of actual and anticipated recruitment rates30 days post dischargeActual rates of recruitment as compared to the anticipated recruitment rate of at least 35% of those approached for the study.
Comparison of actual and anticipated retention rates30 days post dischargeActual rates of retention as compared to the anticipated retention rate of 70% of participants until the final survey time point.
Comparison of actual and anticipated attendance rates30 days post dischargeActual rates of attendance rates as compared to the anticipated 3/4 sessions among at least 70% of participants in the music therapy arm.
Comparison of actual and anticipated completion rates30 days post dischargeActual rates of completion rates as compared to the anticipated at least 70% of 15-day and 30-day follow-up measures.
Number of participants report daily music exercise use30 days post dischargeAt least 60% of participants in the music therapy arm reporting use of music exercises at least once every other day.
Acceptance of music therapy intervention37 days post dischargeFavorable responses to qualitative interviews

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026