NCT05044832

Decreasing Emergence Agitation With Personalized Music

Stanford University·ClinicalTrials.gov·behavioralRecruiting
View on ClinicalTrials.gov
Study focus
Drug/Device/Intervention
Personalized Music
Study type
Interventional
Intervention type
behavioral
Sponsor & location
Primary sponsor
Stanford University
Location
Stanford,Burlington, United States of America
Timeline & enrollment
Phase
N/A
Start date
Nov 12, 2021
End date
Nov 01, 2022
Enrollment
100 participants
Primary outcome

Change in Pediatric Anesthesia Emergence Delirium (PAED) scores

Summary

The purpose of the study is to assess the impact of personalized music on emergence agitation
 (EA), as measured by Pediatric Anesthesia Emergence Delirium scores in pediatric patients
 recovering from elective procedures under general anesthesia.
 
 Personalized music may help to decrease EA in children undergoing elective surgeries under
 general anesthesia by decreasing perioperative anxiety and minimizing perceived pain. The
 study has the potential to improve perioperative care by improving safety, decreasing the
 need for postoperative pharmacologic and nursing interventions, thereby shortening the time
 of recovery and improving caregiver satisfaction.
 
 Participants participating in this study will be randomly assigned to receive personalized
 music plus standard of care, or standard of care alone. Those assigned to the music group
 will receive music in the preoperative holding area as well as in the post-operative care
 unit.

ICD-10 classifications
Surgical procedure, unspecifiedMedical procedure, unspecifiedOther surgical proceduresDuring unspecified surgical and medical careDuring unspecified surgical and medical care
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT05044832
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT05044832 through Pure Global AI's free database. This phase not specified trial is sponsored by Stanford University and is currently Recruiting. The study focuses on Surgical Procedure, Unspecified. Target enrollment is 100 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.