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POP SINGER Pilot Study

Pain Management Optimized Through Patient-centered Multi-Session Group Music Therapy Within INteGrative sharEd progRamming: A Single-arm Pilot Study

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07450131
Acronym
POP SINGER 1
Enrollment
22
Registered
2026-03-04
Start date
2026-03-13
Completion date
2026-07-08
Last updated
2026-09-04

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

Conditions

Chronic Pain

Keywords

Music Therapy, Chronic Pain, Group Medical Visits, Virtual

Brief summary

Conduct a single-arm pilot study (N = 24) to examine the feasibility and acceptability of the hybrid (i.e., half in-person, half online) POPSINGER group Music Therapy (MT) intervention.

Interventions

BEHAVIORALMusic Therapy

A board-certified music therapist will provide a total of 16 MT sessions (8 in-person and 8 virtual) that include education, social connection, and experiential music interventions. These sessions will focus on self-management of pain through evidenced-based MT interventions including music sharing, playlists using the iso-principle, music making, music and guided imagery, music and deep breathing, progressive muscle relaxation, and adapted cardio drumming.

Sponsors

University Hospitals Cleveland Medical Center
Lead SponsorOTHER
Kulas Foundation
CollaboratorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults age 18 and older * Reporting pain on most days per month for a duration of ≥3 months * Independently ambulatory * Willing to participate in full scope of program * Access to internet, active email address, \& laptop, tablet, and/or PC with videoconferencing capabilities * Have reliable access to a mobile device with an active data plan at home and is comfortable accessing the internet and their email with this device * Able to read and understand English

Exclusion criteria

* Significant hearing and/or visual impairment * Have had a major surgery (e.g., spine surgery, joint replacement) within the past 6 months * Have a planned surgery within the next 6 months at the time of enrollment * Unable to independently provide consent (i.e., no proxy consent) * Active suicidal ideation * Severe psychological comorbidity (e.g., psychosis, schizophrenia) that would prevent patient from engaging fully in intervention * Receiving active cancer treatment * Diagnosed with medical condition likely to be terminal within 24 weeks * Active substance abuse diagnosis in EHR * Currently receiving music therapy from a professional music therapist

Design outcomes

Primary

MeasureTime frameDescription
Number of participants retained as measured by enrollment logs8 weeks from the first music therapy interventionA retention rate of ≥70% of recruited participants until the final survey time point.
Number of sessions attended per participant as measured by attendance logs8 weeks from the first music therapy interventionAn attendance rate of ≥11/16 sessions among ≥70% of retained participants.
Number of participants completing follow-up measures as measured by data collection logs8 weeks from the first music therapy interventionA measure completion rate of ≥70% of follow-up measures among retained participants.
Number of participants reporting daily music exercise use in REDCap exercise logs8 weeks from the first music therapy intervention≥60% of retained MT participants reporting use of music exercises at least once every other day.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORAngelique Foss, CHES®, NBC-HWC, LPMT, MT-BC

University Hospitals Cleveland Medical Center

STUDY_DIRECTORSamuel N Rodgers-Melnick, PhD, MPH, LPMT, MT-BC

University Hospitals Cleveland Medical Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 5, 2026