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Music-based Treatments and Pain: Underlying Mechanisms and the Beneficial Effects of Music-Based Treatments

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University of Washington

Status

Completed

Conditions

Chronic Low-back Pain

Treatments

Behavioral: Control group
Behavioral: Music Therapy
Behavioral: Music Medicine

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05578781
STUDY00014335
1R21AT011577-01A1 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The purpose of this study is to understand the mechanisms that underlie the beneficial effects of music-based treatments in individuals with moderate to severe chronic low back pain

Full description

A growing body of research indicates that music may be used effectively for improving a variety of symptoms, including pain. However, little is known about the mechanisms that underlie the beneficial effects of music-based treatments. The primary objective of this R21 exploratory study is to evaluate the feasibility of performing a full R01 study in a sample of individuals with moderate to severe chronic low back pain to address knowledge gaps regarding the mechanisms of music-based treatments. To address the primary aims of this study, the investigators will conduct a 3-arm pilot trial in which individuals with chronic low back pain will be randomly assigned to one of three conditions: (1) live music played by a board-certified music therapist (Music Therapy), (2) audio recorded music (Music Medicine), or (3) audio of a person reading written text (n = 20 subjects per condition). In addition, 20 individuals without chronic pain will be enrolled and assigned to the Music Medicine condition.

An EEG assessment measuring brain oscillation spectral power will be conducted before and during a session of each experimental condition. Measures of pain intensity will be administered before and after the sessions. Low back pain was selected because it is among the most common, costly, and disabling chronic pain problems; including a non-pain sample will also allow us to determine if having chronic pain or not influences the effects of music on the primary mechanism variables. Effect sizes will be computed to evaluate (1) the effects of the treatments on frontal midline theta power and (2) the mediation effects of changes in frontal midline theta power on the pre- to post-session effects of the music conditions, relative to the control condition. The investigators will also investigate the differences between the three music conditions, compare the effects of Music Medicine on the mechanism variables as a function of having or not having chronic pain, and explore the extent to which the experimental conditions have lingering effects on pain intensity and secondary outcomes (depression, pain interference, and sleep quality) during the 24 hours after the experimental sessions. The investigators will also perform interviews and qualitative data analyses to identify additional unanticipated effects of the experimental conditions that would be worth examining more closely in a full R01 study. The findings from this study will be used to determine if a full R01 study to evaluate the mechanisms of music-based treatments is warranted, and to inform the design of such as study. This program of research will provide important foundational knowledge regarding the mechanisms of music-based interventions. Transferred to clinical care, this knowledge could help in patient-treatment matching which would enhance the overall effectiveness for music-based treatments and other non-pharmacological treatments that may operate via their effects on brain states, as measured by EEG.

Enrollment

99 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria for Chronic Low Back Pain sample:

  • ≥18 years old
  • Meets criteria for Chronic Low Back Pain (CLBP)
  • Moderate to severe pain intensity on average (i.e., average pain in the past week ≥4 on the 0-10 NRS)
  • Able to read, speak, and understand English

Inclusion criterion for the non-pain sample:

  • ≥18 years old
  • Able to read, speak, and understand English

Exclusion Criteria:

  • Cognitive impairment that could interfere with study participation defined as ≥1 error on the 6-Item
  • Presence of a psychiatric condition (e.g. significant suicidal ideation, active psychotic symptoms that would interfere with study participation
  • Having a significant hearing disability that interferes with the potential participant's ability to hear music
  • Having a health condition associated,per both chart review and self-report, with central nervous system damage (e.g., epilepsy, traumatic head injury, multiple sclerosis, Parkinson's).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

99 participants in 4 patient groups

Music Therapy
Experimental group
Description:
The Music Therapy (MT) group will participate in 1 live session of music therapy with a board certified Music therapist while wearing an EEG cap. Afterwards, they will complete a brief questionnaire about the experience and pain. They will also complete a brief questionnaire 24 hours later about lasting effects and pain
Treatment:
Behavioral: Music Therapy
Music Medicine
Experimental group
Description:
The Music Medicine (MM) group will participate in 1 audio session of music while wearing an EEG cap. Afterwards, they will complete a brief questionnaire about the experience and pain. They will also complete a brief questionnaire 24 hours later about lasting effects and pain
Treatment:
Behavioral: Music Medicine
Control condition
Experimental group
Description:
the Control group will participate in 1 session of an audio of text being read to them while wearing an EEG cap. Afterwards, they will complete a brief questionnaire about the experience and pain. They will also complete a brief questionnaire 24 hours later about lasting effects and pain
Treatment:
Behavioral: Control group
Control group without low back pain
Active Comparator group
Description:
This group will participate in 1 session of an audio of the music therapy session while wearing an EEG cap. Afterwards, they will complete a brief questionnaire about the experience and pain. They will also complete a brief questionnaire 24 hours later about the lasting effects and pain
Treatment:
Behavioral: Control group

Trial contacts and locations

1

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Central trial contact

Kevin Gertz; Erica Wasmund

Data sourced from clinicaltrials.gov

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