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临床试验/NCT04159584
NCT04159584已完成不适用

Pilot Study: The Effects of Medical Music on Anxiety in Patients With Interstitial Lung Disease

Weill Medical College of Cornell University1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2019年4月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
10
试验地点
1
主要终点
Feasibility of using a medical music intervention as a treatment for anxiety in subjects with ILD, as measured by descriptive evaluation.

研究概览

简要总结

This is uncontrolled, interventional feasibility study for determining the effects medical music on anxiety levels in subjects with ILD. Enrolled subjects will be asked to complete questionnaires and undergo physiologic measurements prior to listening to medical music. The music intervention will be for approximately 30 minutes. Post intervention questionnaires and physiologic measurements will be done.

详细描述

The Medical Music intervention includes playlists that contains songs specifically designed, recorded, and optimized through the provisionally-patented methods, to treat their co-morbid anxiety. The duration of the medical music playlist is 30 minutes.

Enrolled subjects will be asked to complete questionnaires to assess anxiety, a questionnaire related to their music preferences, and undergo physiological measurements (vital signs, galvanic skin response, and heart rate variability) before and after the intervention.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
50 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Men and women age 50 to 80 years old
  • Diagnosis of definite or probable interstitial lung disease (ILD)
  • Willingness to participate and sign consent

排除标准

  • Patients who are deaf
  • Inability to provide informed consent
  • Pregnant women

结局指标

主要结局

Feasibility of using a medical music intervention as a treatment for anxiety in subjects with ILD, as measured by descriptive evaluation.

时间窗: Baseline to 30 minutes

次要结局

  • Change in State Anxiety Inventory scores before and after intervention(Baseline to 30 min)
  • Change in heart rate variability before and after intervention(Baseline to 30 min)
  • Change in Visual Analogue Scale scores for Anxiety and Distress (VAS-A) before and after intervention(Baseline to 30 min)
  • Change in Borg Dyspnea Scale scores before and after intervention(Baseline to 30 min)
  • Change in galvanic skin response before and after intervention(Baseline to 30 min)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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