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临床试验/NCT06993441
NCT06993441已完成不适用

Effects of Music on Pain, Anxiety and Stress Levels in Cancer Patients Receiving Radiotherapy

Ege University1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2024年4月4日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
120
试验地点
1
主要终点
Pain Level

研究概览

简要总结

This randomized controlled study aims to evaluate the effects of music therapy administered during radiotherapy sessions on pain, stress, and anxiety levels in cancer patients. The intervention involves playing Musicure, a therapeutic music track, for 30 minutes via speakers during radiotherapy. The study includes two groups: an intervention group receiving music therapy and a control group receiving standard care without music.

Participants' pain levels were assessed using the Visual Analog Scale (VAS), while anxiety and stress levels were measured using the Face Anxıety Subscale ( FAS).

A total of 120 adult cancer patients undergoing outpatient radiotherapy at Tınaztepe Unıversty were included. The study was conducted under the supervision of Dr. Öğr. Üyesi [Duygu AKBAŞ UYSAL (Principal Investigator) and co-researchers Prof.Dr Fsun ŞENUZUN AYKAR, Prof.Dr Zümra ARICAK ALICIKUŞ The research complies with ethical standards and has received approval from [insert name of ethics committee].

This study investigates a low-cost, non-pharmacological intervention that has the potential to improve symptom management and quality of life in cancer patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Volunteer to participate in the study,
  • •18 years of age and older,
  • •No hearing problems,
  • •No communication and speech problems

排除标准

  • •Those diagnosed with psychiatric and neurological diseases,

研究组 & 干预措施

Experimental Arm

Experimental

Participants in this group will listen to MusICure music through speakers for 30 minutes during each radiotherapy session. The intervention is designed to provide a calming auditory experience to reduce anxiety and improve comfort during treatment.

干预措施: Experimantal group (Behavioral)

control group

Experimental

干预措施: control group (Behavioral)

结局指标

主要结局

Pain Level

时间窗: Baseline (before radiotherapy on Day 1) and immediately after the radiotherapy session on Day 1.

Changes in pain levels were assessed using the Visual Analog Scale (VAS) immediately before and after a single radiotherapy session. The VAS score ranges from 0 (no pain) to 10 (worst possible pain).

次要结局

  • anxiety level(Baseline (before radiotherapy on Day 1) and immediately after the radiotherapy session on Day 1.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Duygu Akbas Uysal

Dr.

Ege University

研究点 (1)

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