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Decreasing Emergence Agitation With Personalized Music

Primary Purpose

Surgical Procedure, Unspecified

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Personalized Music
Sponsored by
Stanford University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Surgical Procedure, Unspecified focused on measuring eardrum procedures, laser treatment for skin lesions, adenoidectomy without tonsillectomy, tonsillectomy with or without adenoidectomy

Eligibility Criteria

3 Years - 9 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria

  • patient ages 3-9 (chosen due to high incidence of emergence delirium and presence of musical memory seen in this age group)
  • unilateral or bilateral myringotomy procedure, laser treatment for skin lesions, adenoidectomy without tonsillectomy
  • tonsillectomy with or without adenoidectomy

Exclusion Criteria

  • Chronic intake of any sedative or analgesic medication
  • Combined surgical procedure not otherwise listed in inclusion criteria
  • Surgical or anesthetic complications (including use of invasive airway device for myringotomy)
  • History of significant hearing loss impeding the ability to hear music
  • Lack of interest in music reported by parents or inability to identify personally meaningful music

Sites / Locations

  • Stanford UniversityRecruiting
  • University of Vermont Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Personalized Music

Standard of Care

Arm Description

Those assigned to the music group will receive music in the preoperative holding area as well as in the post-operative care unit in addition to standard care.

Those assigned to the Standard of Care arm will only receive standard of care in the preoperative holding area as well as in the post-operative care unit

Outcomes

Primary Outcome Measures

Change in Pediatric Anesthesia Emergence Delirium (PAED) scores
Personalized music may help to decrease EA in children undergoing elective surgeries under general anesthesia by decreasing perioperative anxiety and minimizing perceived pain. PAED scores range from 0 to 20; a score of 10 and above is defined as emergence agitation.

Secondary Outcome Measures

Change in modified Yale Preoperative Anxiety Scale (mYPAS) score
mYPAS scores range from 23.3-100; a score of 30 and above is defined as high anxiety
Change in patient response to personalized music in relation to parental anxiety using State and Trait Anxiety (STAI) scores (parent-reported)
STAI is broken into two parts (STAI-S and STAI-T); scores range from 20-80 ; a STAI-S score of 40 and above is defined as high state anxiety, a STAI-T score of 52 and above is defined as high trait anxiety
Change in mask acceptances using Induction Compliance Checklist (ICC)
ICC scores range from 0-10, with 0 being a perfect induction
Change in parental satisfaction with the patient's perioperative experience using a post-operative parental satisfaction survey
Parent/guardian satisfaction will be assessed with a qualitative 6 question survey
Change in post-operative pain
FLACC and Wong-Baker scores each range from 0-10

Full Information

First Posted
September 8, 2021
Last Updated
October 16, 2023
Sponsor
Stanford University
Collaborators
University of Vermont Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT05044832
Brief Title
Decreasing Emergence Agitation With Personalized Music
Official Title
Decreasing Emergence Agitation With Personalized Music
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
November 12, 2021 (Actual)
Primary Completion Date
November 2024 (Anticipated)
Study Completion Date
November 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Stanford University
Collaborators
University of Vermont Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief 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.
Detailed Description
Study Protocol: This is a prospective, randomized controlled trial of children 3-9 years of undergoing non-complex ENT procedures to assess the impact of perioperative personalized music on the incidence of emergence agitation (EA). There will be 2 groups in the study: Personalized music group Standard care group All patients enrolled in this study will receive a standardized anesthetic consistent with standard practice at the Stanford Children's Hospital based on their type of procedure: Patients undergoing myringotomies will receive: Oral midazolam (0.5mg/kg up to a maximum of 20mg) preoperatively, unless clinically contraindicated Inhalational induction of anesthesia, either with a combination of nitrous oxide and sevoflurane or 8% sevoflurane, depending on provider preference and clinical context A combination of fentanyl (1 mcg/kg) and ketorolac (0.5 mg/kg) given in a single intramuscular (IM) injection, given while under anesthesia in the operating room. Patients undergoing tonsillectomies will receive an anesthetic regimen consistent with common practice at Lucile Packard Children's Hospital While these anesthetic regimens will serve as the default for study patients, the perioperative care team may deviate if clinically warranted in their judgement. All patients will be assessed post-operatively for emergence delirium using the Pediatric Anesthesia Emergence Delirium (PAED) assessment tool (described in "Procedures"). All patients will also be assessed for anxiety using the modified Yale Preoperative Anxiety Scale (mYPAS) while in the preoperative area. Patients will also be assessed for mask acceptance on induction of anesthesia (ICC), and pain after their procedure using the FLACC, Wong-Baker FACES, or VAS scale (appropriate scale will be determined based on patient age and clinical context). All patient guardians will be assessed for anxiety using the State-Trait Anxiety Inventory (STAI) during the procedure (described in "Procedures"). These assessments are validated for use in this age group. Data collection: Patient demographic information, clinical documentation (clinic notes, procedure reports, labs, anesthesia records, imaging reports etc.) will be collected. Data collection sheet attached. Data analysis: Pediatric Anesthesia Emergence Delirium (PAED) scores will be used as our primary outcomes measure to assess for emergence agitation, which is a 20-point scale and assumes a normal distribution. The investigators plan to collect six PAED scores for each patient taken at 10 minute intervals following completion of each procedure for all participants. Participants will be divided randomly into two groups: half with music, and half without music. The Investigators anticipate an incidence of emergence agitation in the range of 10-20% (defined as a PAED score of 12 or greater) based our subject group and literature review. To assess for a difference in PAED scores between groups, with a Type 1 error of 0.05, and a power of 0.8, the investigators estimate a need of 40 participants per group (80 participants total) to detect an effect size of 0.3. The investigators plan to recruit 100 total participants in order to account for potential withdrawals or protocol deviations. Secondary measures of interest include the modified Yale Preoperative Anxiety Scale (mYPAS), mask acceptance, and post-operative pain. Data Safety Monitoring Plan: The principal investigator will review subject enrollment, adverse events, unanticipated occurrences, and protocol deviations. Any adverse events meeting criteria will be reported to the IRB. The investigators will follow the guidelines in the IRB's Adverse Event and Unanticipated Problems Reporting Policy. Significance: 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Surgical Procedure, Unspecified
Keywords
eardrum procedures, laser treatment for skin lesions, adenoidectomy without tonsillectomy, tonsillectomy with or without adenoidectomy

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Personalized Music
Arm Type
Experimental
Arm Description
Those assigned to the music group will receive music in the preoperative holding area as well as in the post-operative care unit in addition to standard care.
Arm Title
Standard of Care
Arm Type
No Intervention
Arm Description
Those assigned to the Standard of Care arm will only receive standard of care in the preoperative holding area as well as in the post-operative care unit
Intervention Type
Behavioral
Intervention Name(s)
Personalized Music
Intervention Description
Personalized music delivered during the perioperative and post-operative periods. Those assigned to the music group will receive music in the preoperative holding area as well as in the post-operative care unit.
Primary Outcome Measure Information:
Title
Change in Pediatric Anesthesia Emergence Delirium (PAED) scores
Description
Personalized music may help to decrease EA in children undergoing elective surgeries under general anesthesia by decreasing perioperative anxiety and minimizing perceived pain. PAED scores range from 0 to 20; a score of 10 and above is defined as emergence agitation.
Time Frame
During post operative period till the child is fully awake, usually about 45 minutes.
Secondary Outcome Measure Information:
Title
Change in modified Yale Preoperative Anxiety Scale (mYPAS) score
Description
mYPAS scores range from 23.3-100; a score of 30 and above is defined as high anxiety
Time Frame
During the pre-operative period, until the child is asleep under general anesthesia, usually about 20 minutes
Title
Change in patient response to personalized music in relation to parental anxiety using State and Trait Anxiety (STAI) scores (parent-reported)
Description
STAI is broken into two parts (STAI-S and STAI-T); scores range from 20-80 ; a STAI-S score of 40 and above is defined as high state anxiety, a STAI-T score of 52 and above is defined as high trait anxiety
Time Frame
During the intra-operative period, usually about 20 minutes
Title
Change in mask acceptances using Induction Compliance Checklist (ICC)
Description
ICC scores range from 0-10, with 0 being a perfect induction
Time Frame
During the intra-operative period, usually about 5 minutes
Title
Change in parental satisfaction with the patient's perioperative experience using a post-operative parental satisfaction survey
Description
Parent/guardian satisfaction will be assessed with a qualitative 6 question survey
Time Frame
During the post-operative period, usually about 45 minutes
Title
Change in post-operative pain
Description
FLACC and Wong-Baker scores each range from 0-10
Time Frame
During the post-operative period, usually about 20 minutes

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
9 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria patient ages 3-9 (chosen due to high incidence of emergence delirium and presence of musical memory seen in this age group) unilateral or bilateral myringotomy procedure, laser treatment for skin lesions, adenoidectomy without tonsillectomy tonsillectomy with or without adenoidectomy Exclusion Criteria Chronic intake of any sedative or analgesic medication Combined surgical procedure not otherwise listed in inclusion criteria Surgical or anesthetic complications (including use of invasive airway device for myringotomy) History of significant hearing loss impeding the ability to hear music Lack of interest in music reported by parents or inability to identify personally meaningful music
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
R J Ramamurthi, MD
Organizational Affiliation
Stanford University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Stanford University
City
Stanford
State/Province
California
ZIP/Postal Code
94305
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Benajamin Sanofsky, MD
Phone
330-417-5544
Email
sanofsky@stanford.edu
First Name & Middle Initial & Last Name & Degree
R J Ramamurthi
Phone
650-776-6297
Email
rjram@stanford.edu
First Name & Middle Initial & Last Name & Degree
Benjamin Sanofsky, MD
First Name & Middle Initial & Last Name & Degree
R J Ramamurthi, MD
Facility Name
University of Vermont Medical Center
City
Burlington
State/Province
Vermont
ZIP/Postal Code
05401
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alex Friend
Phone
802-847-4259
Email
alexander.friend@uvmhealth.org

12. IPD Sharing Statement

Plan to Share IPD
No

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Decreasing Emergence Agitation With Personalized Music

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