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临床试验/NCT06670027
NCT06670027已完成不适用

The Effects of Using Auditory Stimulation Methods on Cardiac Patients' Clinical Outcomes

Damanhour University1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2024年7月1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
80
试验地点
1
主要终点
severity of chest pain

研究概览

简要总结

This study will be used to compare the effects of two auditory stimulation methods on improving vital signs parameters, reducing the severity of chest pain, and improving the sleep quality of cardiac patients.

详细描述

This study aims to To evaluate the relative efficacy of two auditory stimulation techniques in enhancing cardiac patients' vital sign assessments.

  • This study aims to examine two auditory stimulations for their ability to alleviate chest pain in patients with heart conditions.
  • The goal of this study is to evaluate two audio stimulations for their potential to help heart patients have a better night's rest.

This research made use of two different therapies including audio stimulation. Group A used familiar auditory stimulus, which was a spoken message, and group B used sounds of nature.

Patients with preexisting cardiac conditions who were admitted to a predetermined critical care unit and who subsequently intended to have percutaneous coronary artery intervention (PCI)

研究设计

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

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • adult (aged≥18 years).
  • diagnosed with cardiac disease.
  • patient with hemodynamic stability
  • consciousness and ability to communicate.

排除标准

  • patients unable to comply with study interventions
  • patients with cognitive impairment
  • patients with severe unstable cardiac condition
  • having a history of hearing loss or the use of a hearing aid.

结局指标

主要结局

severity of chest pain

时间窗: three days after intervention

Visual analogue scale consisted of score from 0 to 10 zero mean no pain and 10 mean high pain

sleep quality

时间窗: three days after intervention

sleep quality used Richards-Campbell Sleep Questionnaire (RCSQ). it consisted of five items score from zero mean poor pattern and 100 mean good

level of anxiety and depression

时间窗: three days after intervention

The hospital Anxiety and Depression (HAD) questionnaire consisted of 14 questions 7 for anxiety and 7 for depression score score 0-7 mean normal; score 8-10 mean mild; score 11-15, mean moderate; and score 16-21, mean severely

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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