Meaning in Music-Based Pain Modulation
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 →
Unsure about the terms? Read our patient guide →
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