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临床试验/NCT07344883
NCT07344883尚未招募不适用

Effects of Music on Pain in Orthopedic Patients With Distal Radius Fractures Undergoing Non-surgical Reduction: a Randomized Controlled Trial

Azienda Unita Sanitaria Locale di Piacenza1 个研究点 分布在 1 个国家目标入组 192 人开始时间: 2026年2月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
192
试验地点
1
主要终点
Difference in Numerical Rating Scale (NRS) pain score between T0 and T1

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Investigator)

盲法说明

Data processing will be blinded

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • Patients with severe hearing impairment
  • Patients diagnosed with cognitive or psychiatric disorders
  • Patients requiring emergency/urgent intervention
  • Open fractures (exposed fractures)

研究组 & 干预措施

Group 1-Patient-preferred music

Experimental

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.

干预措施: Music intervention Group 1 (Other)

Group 2-Standardized music playlist

Experimental

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.

干预措施: Music intervention Group 2 (Other)

Group 3- NO MUSICTHERAPY

No Intervention

The control group will receive standard care without music during the same time interval.

结局指标

主要结局

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

时间窗: Baseline and 20 minutes after baseline

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.

次要结局

未报告次要终点

研究者

发起方
Azienda Unita Sanitaria Locale di Piacenza
申办方类型
Other
责任方
Principal Investigator
主要研究者

Massimo Guasconi

RN, PhD

Azienda Unita Sanitaria Locale di Piacenza

研究点 (1)

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