Music Therapy to Reduce Anxiety and Pain in Chronic Pain Patients During Procedures

Singapore Health Services (SingHealth)

Status: Not yet enrolling

Conditions: Pain Perception; Chronic Pain; Pain Catastrophizing; Anxiety; Music Therapy

Treatments: Behavioral: Music Therapy

Study type: Interventional

Funder types: Other

Identifiers

NCT07252648

2025-1781

Details and patient eligibility

About

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.

Full description

This is a single-centre, randomised controlled trial conducted at the Singapore General Hospital Pain Management Centre. The study investigates whether peri-operative music therapy can reduce anxiety, pain catastrophising, and pain in patients with chronic pain undergoing interventional pain procedures in the ambulatory setting.

A total of 110 adult participants (aged 21 years and above) with chronic pain lasting at least 3 months and scheduled for interventional pain procedures will be enrolled. Participants will be randomised in a 1:1 ratio to either the music therapy group or the control group using a computer-generated block randomisation sequence with sealed opaque envelopes.

Intervention group: Participants will listen to self-selected music from curated playlists (including soothing, meditative, multilingual, and instrumental tracks) before, during, and after the procedure. Music will be played for 30 minutes pre-procedure via headphones, continued intra-procedurally via Bluetooth speaker to maintain communication, and resumed for 30 minutes post-procedure via headphones.

Control group: Participants will receive standard peri-procedural care without music exposure.

Due to the nature of the intervention, blinding of participants and proceduralists is not feasible. However, outcome assessors and statisticians will remain blinded to group allocation.

The primary endpoint is postoperative anxiety measured using the Visual Analogue Scale for Anxiety (VAS-A) and the Hospital Anxiety and Depression Scale (HADS). Secondary endpoints include pain catastrophising scores (Pain Catastrophising Scale, PCS), procedural pain (Numerical Rating Scale, NRS), and patient satisfaction scores.

Data will be collected pre-procedure and immediately post-procedure. Baseline demographics, analgesic/sedative use, and intra-procedural variables (e.g., duration, complications, and rescue medication use) will also be recorded. Statistical analysis will compare mean differences between groups using independent t-tests for continuous variables and chi-square tests for categorical variables, with significance set at p < 0.05.

The study is classified as minimal risk, involving a non-invasive behavioural intervention. No Data Monitoring Committee has been appointed. Oversight will be provided by the Principal Investigator and study mentor, with periodic internal data reviews.

This trial aims to provide evidence for a simple, low-cost, and patient-centred intervention that could enhance peri-procedural comfort and reduce psychological distress in chronic pain patients undergoing day surgery procedures.

Enrollment: 110 estimated patients

Sex: All

Ages: 21+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

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

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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110 participants in 2 patient groups

Music Therapy

Experimental group

Description:

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.

Treatment:

Behavioral: Music Therapy

Standard Care

No Intervention group

Description:

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