Music Intervention for Agitation Reduction in the Pediatric Intensive Care Unit

Critical Illness Clinical Trial

Official title:

Music Intervention for Agitation Reduction in the Pediatric Intensive Care Unit

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03453814
• Other study ID #: STUDY00001771
• Status: Completed
• Phase: N/A
• Start date: November 1, 2018
• Est. completion date: March 1, 2020

Study information

• Verified date: March 2020
• Source: State University of New York at Buffalo
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The objective of this study is to administer music therapy to patients in the pediatric intensive care unit (PICU) in order to observe how music affects patient agitation, vital signs, and overall recovery in the unit.

Description:

This study is a prospective randomized controlled study to observe patients who have been admitted to the PICU with an altered state of agitation according to the Richmond Agitation Sedation Scale (RASS). These patients will be administered music therapy during a controlled setting in the day to observe whether the introduction of music therapy helps reduce the patient's level of agitation, improving their vital signs and overall recovery in the unit. Once patients are enrolled and have signed consents, patients will receive a headset with music or dead air. Therapy times will be selected so that there are minimal disruptions. Total time will be 2 hours daily, once in the morning and once in the evening. The treatments for session 1 and session 2 of the day will be the same (i.e. Music/ Music, No music/No Music).

The investigators hypothesize that applying music therapy in the PICU will decrease agitation, length of stay, and narcotic administration, and normalize heart rate, respiratory rate, and blood pressure.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 26
• Est. completion date: March 1, 2020
• Est. primary completion date: August 1, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 5 Years to 17 Years

Eligibility

Inclusion Criteria:

• PICU patient at Oishei Children's Hospital of Buffalo

• >4 years of age, <18 years of age

• Patients with RASS of +1

Exclusion Criteria:

• Documented underlying psychological disorders

• Diagnosed with sever developmental delay

• Prior narcotic dependence

• Underlying medical conditions affecting heart rate, blood pressure, or neuromuscular system

• Chemically paralyzed patients

• Anyone with an aneurysm

• Patients who are deaf in both ears

• Ear bone fractures or other middle/inner ear trauma or major ear avulsion as determined by physician

• Hemodynamically unstable patients

• Patients facing imminent death

Related Conditions & MeSH terms

• Critical Illness
• Psychomotor Agitation

Intervention

Other:
• Music Therapy
Subjects will receive one hour of music twice a day for three days.

Locations

Country	Name	City	State
United States	Oishei Children's Hospital	Buffalo	New York

Sponsors (1)

Lead Sponsor	Collaborator
State University of New York at Buffalo

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Richmond Agitation-Sedation Scale (RASS)	The Richmond Agitation-Sedation Scale (RASS) is a medical scale used to measure the agitation or sedation level of a patient. The scale measures patient agitation and sedation +4 to -5, with a score of 0 equal to an alert and calm patient, a positive score equal to various levels of aggression, and a negative score equal to various levels of sedation. Patients receive one score for one observed time point. Therefore, a patient will have one score from +4 to -5. For the purpose of this study, a better outcome will be a score that is around 0 or that decreases from a higher positive score to a lower positive score. The investigators hypothesize that music therapy will decrease agitation in patients and decrease their positive RASS score.	3 days
Secondary	Bispectral Index (BIS)	The Bispectral Index provides a direct measure of the effects of sedatives on the brain. It is an algorithm developed by Aspect Medical Systems that measures EEG after the administration of anesthetic agents and is measure on a BIS monitor. The BIS monitor reports a single number from 0 to 100 that represents an integrated measure of cerebral electrical activity. This is interpreted into a patient's level of alertness. A score of 100 indicates that the patient is fully awake, while a number less than 40 is suggestive of a deep hypnotic effect. For the purpose of this study, the investigators are using the BIS to measure the level of alertness in a patient. The investigators hypothesize that the administration of music therapy with have a sedative effect on patients, thereby decreasing their BIS number.	3 days