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Recruiting NCT07036315

Meaning in Music-Based Pain Modulation

No phase Interventional The Focus of the Study is Healthy Volunteers

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Music intervention.
Who it may be relevant to
Registry conditions: The Focus of the Study is Healthy Volunteers. Basic parameters: 18 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

An Investigation of the Intersection of Affect and Meaning in Music-Based Pain Modulation

Overview

The overall goal of this project is to examine the impact of music's meaning on pain. Relationships between trait affect, meaning in life, and subjective qualities of meaningful music will be assessed. We will also conduct interviews with a subset of participants to determine which aspects of music are most meaningful and how this meaning increases or decreases pain sensations.

Interventions

  • Other Music intervention
    Participants will be asked to select different music clips based on meaning, enjoyment and preference.

Primary outcome measures

  • Pain Unpleasantness [Time frame: Baseline/Pre-intervention and During the Intervention]
  • Pain Intensity [Time frame: Baseline/Pre-intervention and During the Intervention]
Secondary outcome measures (5)
  • The Multidimensional Meaning in Life Scale [Time frame: Baseline/Pre-intervention]
  • The Positive and Negative Affect Schedule-X (PANAS-X) [Time frame: Baseline/Pre-Intervention]
  • The Hedonic and Eudaimonic Motives for Activities Scale [Time frame: Baseline/Pre-intervention]
  • The Geneva Emotional Music Scale [Time frame: During the Intervention]
  • Optional Micro-Phenomenological Interview [Time frame: Immediately After the Intervention]

Eligibility criteria

Inclusion criteria

  • 18-65 years old
  • Absence of acute or chronic pain
  • Normal hearing (either naturally or with assistance of hearing device)
  • Must be able to wear an EEG
  • Able to sign consent

Exclusion criteria

  • < 18 or > 65 years old
  • Presence of acute pain (brief pain inventory score > 3)
  • Pregnant women
  • Participant reports that they experience pain on more days than not in the past 6 months (i.e., chronic

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Basic science

Study locations

United States · 1 center
  • University of Virginia — Charlottesville

Identifiers

NCT: NCT07036315 · HSR 230193 · U24AT012601

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗