Effects of Music on Procedural Pain in Distal Radius Fracture Reduction

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAzienda Unita Sanitaria Locale di Piacenza

About this trial

This randomized controlled trial (RCT) evaluates the effectiveness of music as a complementary intervention for pain control during non-surgical reduction of distal radius fractures in orthopedic patients. Distal radius fractures are among the most common traumatic injuries presenting to emergency departments and are frequently associated with intense procedural pain and significant physiological stress responses. Despite standard pharmacological analgesia, optimal pain management during fracture reduction remains a clinical challenge, and evidence regarding non-pharmacological adjuncts in the emergency orthopedic setting is still limited The study will enroll 192 adult patients admitted to the orthopedic emergency departments of AUSL Piacenza and AOU Parma with distal radius fractures requiring closed reduction. Participants will be randomly assigned (1:1:1) to one of three groups: a 20-minute session of patient-preferred music, a 20-minute session of standardized music selected by a music therapist, or standard care without music. Pain intensity will be assessed using the Numerical Rating Scale (NRS), while physiological stress will be evaluated through heart rate and blood pressure measurements, collected at baseline (T0) and 20 minutes later (T1), immediately after the reduction procedure The trial is designed as a prospective, randomized, controlled study with blinded data analysis, and all data will be collected and managed in compliance with current privacy and data protection regulations. By generating robust evidence on a low-cost, safe, and easily implementable intervention, the PolSound trial aims to improve procedural pain management and patient experience in emergency orthopedic care, potentially supporting the integration of music-based interventions into standard analgesic protocols.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients of both sexes, 18 years of age or older

Patients with distal radius fracture requiring non-surgical (closed) reduction

Able to provide informed consent

Disqualifiers

Patients with severe hearing impairment

Patients diagnosed with cognitive or psychiatric disorders

Patients requiring emergency/urgent intervention

Open fractures (exposed fractures)

Trial design

Design model

Parallel

Treatments tested in this trial

  • Music intervention Group 1

    Other intervention

    After enrolment and baseline assessment (NRS, heart rate, blood pressure - T0), patients allocated to the intervention groups will receive a 20-minute music session before fracture reduction, followed by reassessment of outcomes at T1 and CRF completion. Group 1 will listen to patient-preferred music via headphones. Music will be administered at the patient's bedside or in the treatment area, ensuring privacy, minimal distractions, and patient comfort.

  • Music intervention Group 2

    Other intervention

    After enrolment and baseline assessment (NRS, heart rate, blood pressure - T0), patients allocated to the intervention groups will receive a 20-minute music session before fracture reduction, followed by reassessment of outcomes at T1 and CRF completion. Group 2 will listen to a standardized music playlist selected by a music therapist (instrumental, slow tempo 60-80 BPM, stable dynamics, moderate volume). Music will be administered at the patient's bedside or in the treatment area, ensuring privacy, minimal distractions, and patient comfort.

Treatment groups

192 Participants
are divided into 3 treatment groups
Group A: Group 1-Patient-preferred musicExperimental treatment 1 intervention
Group B: Group 2-Standardized music playlistExperimental treatment 1 intervention
Group C: Group 3- NO MUSICTHERAPYNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Difference in Numerical Rating Scale (NRS) pain score between T0 and T1

Difference in procedural pain intensity after 20 minutes compared with baseline, evaluated by NRS scores between T0 and T1. The NRS is an 11-point numeric scale ranging from 0 (no pain) to 10 (worst imaginable pain). Higher scores indicate greater pain intensity. A reduction in NRS score reflects improved pain control.

Time frame
Baseline and 20 minutes after baseline

Secondary outcomes

Other outcomes

Sponsors and contacts

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