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临床试验/NCT06848777
NCT06848777已完成不适用

The Effect of Mobilising Patients Using Nature Sounds on Anxiety, Pain and Stress Levels of Patients After Laparoscopic Cholecystectomy Surgery

Akdeniz University2 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2025年3月2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
70
试验地点
2
主要终点
Anxiety

研究概览

简要总结

The Effect of Mobilization Using Nature Sounds on Patients' Anxiety, Pain and Stress Levels

研究设计

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

盲法说明

To ensure that the recording of the data process was unbiased in this study, patients' anxiety and pain levels were assessed by asking patients questions and having them mark their responses on paper under the supervision of the nurse researcher, while the obtained anxiety and pain scores and the stress levels measured using a smartwatch were recorded on the forms by the independent ward nurse. The results of the study findings were analyzed by an independent statistician.

入排标准

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

入选标准

  • •Individuals who are willing to participate in the study,
  • •Patients undergoing their first laparoscopic surgery due to gallbladder stones,
  • •Patients scheduled for elective surgical procedures,
  • •Patients with no hearing impairment,
  • •Patients with no vision impairment,
  • •Mentally stable individuals,
  • •Individuals who are open to communication and cooperation,
  • •Patients aged 18 years and older will be included in the study.

排除标准

  • •Individuals with mental health issues,
  • •Individuals who are unwilling to participate,
  • •Patients with hearing impairment,
  • •Patients undergoing their second surgery (recurrent) due to gallbladder stones,
  • •Patients using hearing aids,
  • •Individuals who are uncooperative or unwilling to communicate,
  • •Patients who require emergency surgery will not be included in the study.

研究组 & 干预措施

Control Group

No Intervention

The standard care protocol of the service will be applied to the patients in the control group. The patients will be mobilized.(

Intervention Group

Experimental

Patients in this group will be mobilized and will be played nature-based sounds through headphones.

干预措施: Intervention group: (Behavioral)

结局指标

主要结局

Anxiety

时间窗: Before mobilization 5 minutes and after mobilization 10 minutes

Anxiety level will be measured withVirtual Analog Scale-Anxiety (The lowest score is set as 0, and the highest score is set as 10.)

Stress

时间窗: before mobilization 5 minutes and after mobilization 10 minutes

with smart watch

Pain level

时间窗: before mobilization 5 minutes and after mobilization 10 minutes

Pain level will be measured with Virtual Analog Scale (The lowest score is set as 0, and the highest score is set as 10.)

次要结局

未报告次要终点

研究者

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

Seda Cansu Yeniğün

Lecturer Dr.

Akdeniz University

研究点 (2)

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