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CompletedNCT06960226PainMusic2Updated May 7, 2025

Replication Study: Reducing Pain With Focused Music Listening

An interventional study of Music Listening and Silence Control in Pain, Pain Management and Pain Threshold, sponsored by University of Bergen. Completed at 1 site in Norway. Open to participants aged 19 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-05-07.

Sponsored by University of Bergen · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
61
Allocation
Not applicable
Ages
19 Years to 35 Years
Sex
All
01

Study summary

The goal of this clinical trial is to confirm previous findings that actively tapping along to music can reduce pain more than just listening to music. This study aims to replicate the findings of a previous study (NCT05267795), with one change in how mild pain is created for the experiment. This study involves healthy adults.

The main questions the study aims to answer are:

  1. Does actively tapping along to music lower feelings of pain compared to just listening to music?
  2. Does actively tapping along to music lower feelings of pain compared to being in silence (with or without tapping)?
  3. Is this method of using music and tapping helpful for managing pain?

Researchers will compare the amount of pain participants feel in four different situations:

  1. Listening to music while actively tapping their foot along with it.
  2. Just listening to music while resting their foot.
  3. Actively tapping their foot in silence.
  4. Sitting in silence while resting their foot.

Participants in this study will:

Experience brief moments of mild pain on their forearm. This pain is safely created using a small electrical pulse from a device held gently on the skin by the researcher. (This replaces the pressure method used in the original study).

Sometimes listen to music through headphones, and sometimes sit in silence. Sometimes tap their foot along to the music or a beat, and sometimes rest their foot. Rate how much pain they feel on a number scale after each pain pulse. Answer short questions about their mood during the experiment. Answer questions about how familiar they are with the music and how much they liked it at the end.

Read the detailed description

This study is a pre-registered replication of a previous trial (NCT05267795) investigating the analgesic effects of sensorimotor synchronization to music. While music listening alone has shown small, albeit reliable, pain-reducing effects, recent theories propose that active synchronization (like tapping or dancing) engages the endogenous opioid system (EOS), potentially leading to stronger analgesia and enhanced social bonding. The original study provided initial evidence supporting this, finding that actively tapping to music significantly reduced experimentally induced pain compared to passive music listening or silence conditions.

This replication study aims to confirm the primary finding that sensorimotor synchronization to music significantly reduces pain perception compared to passive music listening and control conditions. The study employs a 2x2 within-subjects factorial design with two factors: Auditory Condition (Music vs. Silence) and Task Condition (Active Tapping vs. Passive Control). Healthy adult participants will undergo all four conditions.

The primary methodological difference from the original study is the method of pain induction. Instead of pressure algometry, this study will use non-invasive transcutaneous electrical stimulation applied to the participant's forearm via a BIOPAC HSTM01 certified stimulus device. This change was implemented to allow for potentially greater precision and control over the stimulus intensity compared to manual pressure application. Pain intensity will be individually calibrated for each participant based on their pain threshold, ensuring only mild to moderate pain levels are experienced. Safety protocols, including screening for contraindications (e.g., pacemakers, epilepsy, pregnancy, local malignancies) and continuous monitoring, are in place.

Consistent with the original study, perceived pain intensity will be the primary outcome measure, rated on a numerical scale after each stimulus. Secondary measures, including ratings of emotional state (pleasantness, arousal), music familiarity, and music preference, will be collected to explore potential attentional and emotional mechanisms underlying the observed effects, as suggested by the original research. This replication seeks to provide robust evidence regarding the potential for active musical engagement, specifically sensorimotor synchronization, as a tool for pain management.

02

Conditions studied

  • Pain
  • Pain Management
  • Pain Threshold
  • Painful
  • Pain Intensity
  • Pain Intervention
  • Psychomotor Performance
  • Healthy Volunteers

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Keywords

  • Pain
  • Pain Perception
  • Experimental Pain
  • Analgesia
  • Music
  • Music Listening
  • Sensorimotor Synchronization
  • Tapping
  • Rhythm
  • Electrical Pain Stimulation
  • Replication Study
  • Endogenous Opioid System
  • Attention
  • Emotion
  • Affect
  • Pain Management
  • Music Therapy
03

In context

Pain

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

This study's enrollment of 61 is below the median of 70 across 1,904 interventional studies indexed under Pain.

Browse Pain studies →

Lead sponsor

University of Bergen is the lead sponsor of 141 studies on the registry; 19 are open to participants now.

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

04

Who can participate

Ages eligible
19 Years to 35 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Age 18 years or older
  • Self-reported good general health
  • Able to understand study procedures and provide informed consent
  • Normal or corrected-to-normal hearing (sufficient for music perception)

Exclusion criteria

Exclusion Criteria:

  • Contraindications for Electrical Stimulation:

    • Presence of active electronic implants (e.g., cardiac pacemaker, cochlear implant)
    • Pregnancy (self-reported)
    • History of Epilepsy or seizure disorder
    • Presence of local malignancy (especially near the stimulation site on forearm)
    • Broken skin, wounds, or significant skin conditions on the right forearm (stimulation site)
  • Medical/Neurological History:

    • History of significant psychiatric or neurological disease (other than epilepsy, listed above)
    • History of substance dependence
    • Current diagnosis of a chronic pain condition
  • Medication Use:

    • Current regular use of prescription analgesic (pain-relief) medication
    • Current regular use of psychoactive medication
  • Study-Specific:

    • Self-reported musical anhedonia (inability to derive pleasure from music)
    • Significant hearing impairment preventing clear perception of the music
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
61 participants (actual)

Study arms

  • Experimental
    Within-Subjects Conditions

    All participants experience all conditions in a 2x2 within-subjects factorial design. Interventions manipulate two factors: 1. Auditory Condition: Participants listen to selected music (via headphones) or experience silence. 2. Task Condition: Participants perform Active Sensorimotor Synchronization (syncing foot taps/head nods to music or pacing stimulus) or maintain Passive Control (remaining still). Each participant completes trials for all 4 resulting conditions: Music+Active, Music+Passive, Silence+Active, Silence+Passive. Condition order is counterbalanced across participants. During trials, brief non-invasive electrical pain stimuli (BIOPAC system) are delivered to the forearm; intensity is individually calibrated based on pain threshold. Key outcomes (perceived pain, emotional state ratings) are collected.

    Other: Music Listening · Other: Silence Control · Other: Active Sensorimotor Synchronization · Other: Passive Control Task

Interventions

  • OtherMusic Listening

    Participants listen to selected instrumental music excerpts presented via headphones during designated experimental trials.

  • OtherSilence Control

    Participants experience periods of silence with no music presented via headphones during designated control trials. This serves as the auditory control condition compared to Music Listening.

  • OtherActive Sensorimotor Synchronization

    Participants actively synchronize movements (such as foot tapping and/or head nodding) by timing them with the rhythm of the presented music or with a pacing stimulus provided during silent trials.

  • OtherPassive Control Task

    Participants remain still and do not perform specific instructed synchronized movements during designated control trials. This serves as the motor task control condition compared to Active Sensorimotor Synchronization.

06

What researchers measure

Primary outcomes

  1. Perceived Pain

    rated on a scale ranging from 1 to 9 (1 = very little, 5 = medium, 9 = very strong)

    Time frame: Time Frame: 40 minutes (duration of time over which each participant is assessed)

Secondary outcomes

  1. Emotional state with regard to felt pleasantness

    rated on a scale ranging from 1 to 9 (1 = very uncomfortable, 5 = medium, 9 = very comfortable)

    Time frame: Time Frame: 40 minutes (duration of time over which each participant is assessed)

  2. Emotional state with regard to felt arousal

    rated on a scale ranging from 1 to 9 (1 = very calm, 5 = medium, 9 = very activated)

    Time frame: Time Frame: 40 minutes (duration of time over which each participant is assessed)

Other outcomes

  1. Familiarity with the music excerpt (only during trials with music)

    rated on a scale ranging from 1 to 9 (1 = not at all, 5 = partially known, 9 = well known)

    Time frame: Time Frame: 40 minutes (duration of time over which each participant is assessed)]

  2. Liking ratings for each musical excerpt

    rated on a scale ranging from 1 to 9 (1 = strongly disliked, 5 = medium, 9 = strongly liked)

    Time frame: Time Frame: 5 min (duration of time over which each participant is assessed)

07

Study locations

1 site
  • University of Bergen
    Bergen, 5003, Norway
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 7, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06960226
Lead sponsor
University of Bergen
Collaborators
The Research Council of Norway, European Research Council
Responsible party
Sponsor
First posted
May 7, 2025
Start date
Mar 1, 2025
Primary completion
Apr 20, 2025
Completion
Apr 20, 2025
Last update
May 7, 2025

Study contacts

Stefan Koelsch, PhD
principal investigator · Institute for Biological and Medical Psychology, University of Bergen

Oversight

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

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