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RecruitingNCT07036315Updated Nov 25, 2025

Meaning in Music-Based Pain Modulation

An interventional study of Music intervention in The Focus of the Study is Healthy Volunteers, sponsored by University of Virginia. Recruiting at 1 site in United States. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2025-11-25.

Sponsored by University of Virginia · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Primary completion was expected by Jun 2026, 3 months ago, but the record still lists the study as recruiting.
  • Started Oct 2025; still recruiting 11 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Not applicable
Ages
18 Years to 65 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • The Focus of the Study is Healthy Volunteers

Browse trials for

Keywords

  • Music
  • Pain
  • Meaning
03

In context

Pain

2,219 studies on the registry are indexed under Pain; 917 are open to participants now.

This study's planned enrollment of 50 is below the median of 70 across 1,904 interventional studies indexed under Pain.

Browse Pain studies →

Lead sponsor

University of Virginia is the lead sponsor of 653 studies on the registry; 134 are open to participants now.

Of its 60 completed or terminated interventional studies of FDA-regulated products, 41 (68%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

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
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
50 participants (estimated)

Study arms

  • Experimental
    Pain-Modulation

    Participants will be exposed to different music clips.

    Other: Music intervention

Interventions

  • OtherMusic intervention

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

06

What researchers measure

Primary outcomes

  1. Pain Unpleasantness

    Participants will be asked to report pain unpleasantness on a 1 - 100 visual analogue scale ranging from 0 (no sensation) to 100 (intolerable pain)

    Time frame: Baseline/Pre-intervention and During the Intervention

  2. Pain Intensity

    Participants will be asked to report pain intensity on a 1 - 100 visual analogue scale ranging from 0 (no sensation) to 100 (intolerable pain)

    Time frame: Baseline/Pre-intervention and During the Intervention

Secondary outcomes

  1. The Multidimensional Meaning in Life Scale

    The multidimensional meaning in life scale is a 16 item validated questionnaire that measures judgments about life's meaning including three subscales of coherence, purpose and mattering. Participants respond to each item using a 7-point Likert scale (1 = Very strongly disagree, 7 = Very strongly agree). A higher score indicates a stronger sense of that dimension of meaning in life.

    Time frame: Baseline/Pre-intervention

  2. The Positive and Negative Affect Schedule-X (PANAS-X)

    The Positive and Negative Affect Schedule-X (PANAS-X) is a 60-item measure assessing perceived intensity of various emotions, which are aggregated to form positive and negative affect scales, and a series of subscales. Scores are calculated by summing the numerical values of a 5-point Likert type scale (1 = Very slightly or not at all, 5 = extremely) for each item. Higher scores indicate higher levels of the specific affect being measured.

    Time frame: Baseline/Pre-Intervention

  3. The Hedonic and Eudaimonic Motives for Activities Scale

    The Hedonic and Eudaimonic Motives for Activities scale is a 9 item survey used to assess how participants typically approach activities in daily life. Participants rate each item on a 7-point Likert type scale (1 = not at all, 7 = very much) with higher scores indicating more hedonic or eudaimonic motives for activities.

    Time frame: Baseline/Pre-intervention

  4. The Geneva Emotional Music Scale

    Participants will be asked to rate their affective responses to each music clip on a 9-point Likert-type scale. Higher scores indicate a greater experience of each emotion measured.

    Time frame: During the Intervention

  5. Optional Micro-Phenomenological Interview

    The objective of the interview is to gain in-depth data on participants' thoughts and feelings about what makes music meaningful to them and how such meaning relates to their experience of pain.

    Time frame: Immediately After the Intervention

07

Study locations

1 of 1 sites recruiting
  • University of Virginia
    Charlottesville, Virginia 22903, United States
    • Patrick Finan, Ph.D. · Contact · finanlab@virginia.edu · 4349249514
    • Patrick Finan, Ph.D. · Principal investigator
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 25, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07036315
Lead sponsor
University of Virginia
Collaborators
National Center for Complementary and Integrative Health (NCCIH)
Responsible party
Patrick Finan, PhD (Professor, University of Virginia) — Principal investigator
First posted
Jun 25, 2025
Start date
Oct 25, 2025
Primary completion
Jun 15, 2026 (estimated)
Completion
Aug 15, 2026 (estimated)
Last update
Nov 25, 2025

Study contacts

Claudia Denoue, MD
Contact
TTC8WZ@uvahealth.org
4342436744

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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