NCT07252648

Brief Summary

This study aims to find out whether listening to music before, during, and after pain procedures can help reduce anxiety, pain catastrophising, and acute pain in patients with chronic pain. Music therapy may provide a simple, safe, and non-drug way to help patients relax and feel more comfortable. In this study, adult patients with chronic pain who are scheduled for interventional pain procedures at Singapore General Hospital will be randomly assigned to one of two groups. One group will listen to self-selected music through headphones and speakers before, during, and after the procedure. The other group will receive standard care without music. Researchers will measure anxiety, pain catastrophising, and pain levels before and after the procedure using validated questionnaires. The main outcome will be the level of anxiety after the procedure. Other outcomes include pain catastrophising scores, pain scores during local anaesthetic injection, and overall patient satisfaction. This study will help determine if music therapy can be routinely used to improve comfort and emotional well-being for patients undergoing interventional pain procedures.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
110

participants targeted

Target at P50-P75 for not_applicable chronic-pain

Timeline
8mo left

Started Mar 2026

Shorter than P25 for not_applicable chronic-pain

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress14%
Mar 2026Dec 2026

First Submitted

Initial submission to the registry

November 18, 2025

Completed
10 days until next milestone

First Posted

Study publicly available on registry

November 28, 2025

Completed
4 months until next milestone

Study Start

First participant enrolled

March 30, 2026

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Last Updated

April 29, 2026

Status Verified

October 1, 2025

Enrollment Period

9 months

First QC Date

November 18, 2025

Last Update Submit

April 23, 2026

Conditions

Keywords

Pain CatastrophizingMusic TherapyAnxietyChronic Pain

Outcome Measures

Primary Outcomes (1)

  • Postoperative Anxiety (Visual Analogue Scale)

    Postoperative anxiety will be assessed using the Visual Analogue Scale for Anxiety, a 10-cm scale ranging from 0 (not anxious at all) to 10 (extremely anxious).

    Scores will be recorded before the procedure (baseline) and post-procedure within 30 minutes.

Secondary Outcomes (4)

  • Pain Catastrophising Score

    This will be measured before the procedure (baseline) and post-procedure within 30 minutes.

  • Postoperative Anxiety (State-Trait Anxiety Inventory Short Form)

    This will be measured at baseline (pre-procedure) and post-procedure (within 30 minutes of completion).

  • Postoperative Pain Score

    Participants will rate their pain after the procedure in the recovery area (within 30 minutes).

  • Patient Satisfaction

    Within 30 minutes of the procedure.

Other Outcomes (1)

  • Patient Music Preferences

    Post-procedure within 30 minutes.

Study Arms (2)

Music Therapy

EXPERIMENTAL

Participants will listen to self-selected music before, during, and after the interventional pain procedure via headphones. Bluetooth speakers will be used during the procedure to facilitate communication with the healthcare team.

Behavioral: Music Therapy

Standard Care

NO INTERVENTION

Participants will receive routine peri-procedural care without music therapy.

Interventions

Music TherapyBEHAVIORAL

This intervention consists of perioperative music therapy for patients with chronic pain undergoing interventional pain procedures in the ambulatory setting. Participants in the intervention group will listen to self-selected music for approximately 30 minutes before, during the procedure, and 30 minutes after their procedure. Music will be delivered via headphones pre- and post-procedure and via a Bluetooth speaker during the procedure to facilitate communication with the procedural team.

Music Therapy

Eligibility Criteria

Age21 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • aged ≥21years
  • chronic pain ≥3 months
  • scheduled for interventional pain procedures

You may not qualify if:

  • presence of hearing impairment
  • lack of capacity to consent
  • non-interventional pain procedures, e.g. lignocaine infusion, ketamine infusion
  • pregnant women

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (3)

  • Li G, Yu L, Yang Y, Deng J, Shao L, Zeng C. Effects of Perioperative Music Therapy on Patients with Postoperative Pain and Anxiety: A Systematic Review and Meta-Analysis. J Integr Complement Med. 2024 Jan;30(1):37-46. doi: 10.1089/jicm.2022.0803. Epub 2023 Aug 30.

    PMID: 37646752BACKGROUND
  • Goel SK, Kim V, Kearns J, Sabo D, Zoeller L, Conboy C, Kelm N, Jackovich AE, Chelly JE. Music-Based Therapy for the Treatment of Perioperative Anxiety and Pain-A Randomized, Prospective Clinical Trial. J Clin Med. 2024 Oct 15;13(20):6139. doi: 10.3390/jcm13206139.

    PMID: 39458090BACKGROUND
  • Kakde A, Lim MJ, Shen H, Tan HS, Tan CW, Sultana R, Sng BL. Effect of music listening on perioperative anxiety, acute pain and pain catastrophizing in women undergoing elective cesarean delivery: a randomized controlled trial. BMC Anesthesiol. 2023 Apr 3;23(1):109. doi: 10.1186/s12871-023-02060-w.

    PMID: 37013499BACKGROUND

MeSH Terms

Conditions

Chronic PainAnxiety Disorders

Interventions

Music Therapy

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsMental Disorders

Intervention Hierarchy (Ancestors)

Sensory Art TherapiesComplementary TherapiesTherapeuticsRehabilitationAftercareContinuity of Patient CarePatient CarePsychotherapyBehavioral Disciplines and Activities

Study Officials

  • David Y Chee, MBBS

    Singapore General Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 18, 2025

First Posted

November 28, 2025

Study Start

March 30, 2026

Primary Completion (Estimated)

December 31, 2026

Study Completion (Estimated)

December 31, 2026

Last Updated

April 29, 2026

Record last verified: 2025-10

Data Sharing

IPD Sharing
Will not share