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Effectiveness of Music Intervention on Anxiety and Physiological Responses in Critical Ill Patient

Stroke Clinical Trial

Official title:
Effectiveness of Music Intervention on Anxiety in Critical Ill Patient: Randomized Controlled Trial

Clinical Trial Summary

Music intervention is a non-pharmacological and effective intervention that can alleviate anxiety and agitation in patients undergoing weaning. The effectiveness of music intervention in reducing anxiety of patients in Intensive Care Unit (ICU) is still unknown. The purpose of this study was to examine the effectiveness of music intervention on anxiety, agitation, sleep quality and physiological parameters on patients in ICU. This study was conducted from January to June 2019. A total of 196 hospitalized ICU patients were divided into two groups. Subjects in experimental group received 30 minutes music intervention for 3 days on bedside whereas subjects in control group received routine care only. The primary outcome was anxiety. Agitation Sedation Scale, sleep quality and physical parameters were selected to collect as secondary outcomes.There was no significant difference between the groups at baseline. The results of this study support that music can reduce anxiety and agitation levels in ICU's patient. Nurses can incorporate this intervention into the daily care in order to reduce the discomfort of patients.

Clinical Trial Description

Background:Music intervention is a non-pharmacological and effective intervention that can alleviate anxiety and agitation in patients undergoing weaning. The effectiveness of music intervention in reducing anxiety of patients in ICU is still unknown. Objectives: The purpose of this study was to examine the effectiveness of music intervention on anxiety, agitation, sleep quality and physiological parameters on patients in ICU. Methods: This study was conducted from January to June 2019. A total of 196 hospitalized ICU patients were divided into two groups. Subjects in experimental group received 30 minutes music intervention for 3 days on bedside whereas subjects in control group received routine care only. The primary outcome was anxiety measured by Visual Analog Scale. Richmond Agitation Sedation Scale, Richards-Campbell Sleep Scale and their physical parameters were selected to collect the secondary outcomes. ;

Study Design

Related Conditions & MeSH terms

  • Acute Kidney Injury
  • Cerebral Hemorrhage
  • Craniocerebral Trauma
  • Diabetic Ketoacidosis
  • GastroIntestinal Bleeding
  • Gastrointestinal Hemorrhage
  • Head Injury
  • Heart Disease, Ischemic
  • Heart Diseases
  • Heart Failure
  • Hemorrhage
  • Intracerebral Hemorrhage
  • Ketosis
  • Liver Diseases
  • Myocardial Ischemia
  • Pneumonia
  • Respiratory Failure
  • Respiratory Insufficiency
  • Septic Shock
  • Stroke
  • Trauma
  • Wounds and Injuries
Clinical Trial Details
NCT number NCT04977011
Study type Interventional
Source Min-Sheng General Hospital
Contact
Status Completed
Phase N/A
Start date January 2, 2019
Completion date July 30, 2019
View Details
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