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Music Listening: A Mechanistic Trial

Primary Purpose

Critical Illness

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Live music
Recorded music
Usual care
Sponsored by
University of Pittsburgh
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Critical Illness focused on measuring mechanical ventilation, pain, stress, anxiety

Eligibility Criteria

5 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 5 -17 years old
  • intubated and receiving MV
  • expected to have a PICU stay of >72 hours

Exclusion Criteria:

  • PICU physician is concerned about adverse experience (e.g., intracranial pressure instability)
  • Primary caregiver does not read, write, and speak English
  • The child is not expected to survive the PICU stay
  • The child has deafness in both ears, has a history of musicogenic epilepsy, is receiving neuromuscular blockade infusion
  • The child has a diagnosis of COVID-19.

Sites / Locations

  • UPMC Children's Hospital of PittsburghRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm Type

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Arm Label

Live music > Recorded music > Usual Care

Recorded music > Usual care > Live music

Usual Care > Live music > Recorded music

Live music > Usual Care > Recorded music

Recorded music > Live music > Usual care

Usual care > Recorded music > Live music

Arm Description

Order of conditions for the day

Order of conditions for the day

Order of conditions for the day

Order of conditions for the day

Order of conditions for the day

Order of conditions for the day

Outcomes

Primary Outcome Measures

Change in cortisol pre-post condition
Percent change in saliva-based cortisol level, ng/ml. Reported as median change per condition and included as continuous outcome in linear regression.
Change in Interleukin-6 (IL6) pre-post condition
Percent change in saliva-based IL6 level, pg/ml. Reported as median change per condition and included as continuous outcome in linear regression.
High Frequency (HF) Heart Rate Variability
Trajectory of HF, a biomarker of sympathetic nervous activity. Reported as median value per condition and included as continuous outcome in linear regression.
Low Frequency (LF) Heart Rate Variability
Trajectory of LF, a biomarker of parasympathetic nervous activity. Reported as median value per condition and included as continuous outcome in linear regression.
HF to LF ration (HF/LF) Heart Rate Variability
Trajectory of HF/LF ratio, a biomarker of autonomic nervous system balance. Reported as median value per condition and included as continuous outcome in linear regression.
Standard Deviation of Normal to Normal (SDNN) Heart Rate Variability
Trajectory of SDNN, a biomarker of parasympathetic and sympathetic modulation

Secondary Outcome Measures

Acceptability
Qualitative interviews with participants on intervention benefits, limitations, and optimizations. Reported as themes and sub-themes.
Change in Visual Analogue Scale of Anxiety
Percent change in caregiver self-reported anxiety, scaled 0 [no anxiety] to 100 [extremely anxious]. Reported as median change per condition and included as continuous outcome in linear regression.
Change in Face Legs Activity Consolability and Crying (FLACC)
Percent change in observed pain, as measured by FLACC. Each of the 5 domains (e.g., Face, legs, etcs) is scored 0-2 and combined for a total score of 0 through 10, higher number indicates more pain. FLACC change score will be calculated from scores pre/post each condition. Reported as median change per condition and included as continuous outcome in linear regression.

Full Information

First Posted
September 12, 2022
Last Updated
May 5, 2023
Sponsor
University of Pittsburgh
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
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1. Study Identification

Unique Protocol Identification Number
NCT05541029
Brief Title
Music Listening: A Mechanistic Trial
Official Title
Music Listening Interventions for Children Receiving Mechanical Ventilation: A Mechanistic Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 20, 2023 (Actual)
Primary Completion Date
April 8, 2027 (Anticipated)
Study Completion Date
May 3, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Pittsburgh
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

4. Oversight

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

5. Study Description

Brief Summary
A randomized within-subject crossover trial to compare the effects of live and recorded music listening on biomarkers of stress and pain among children receiving mechanical ventilation in the pediatric intensive care unit.
Detailed Description
Children who are critically ill and receiving mechanical ventilation are at increased risks for experiencing high levels of stress and pain, which negatively impacts immediate and long-term health. The current standard of care for treating stress and pain is to provide analgesic and sedative medications, which are associated with increased risk of delirium and posttraumatic stress disorder. This randomized within-subject crossover trial will compare the effects of live and recorded music listening on biomarkers of stress and pain among children receiving mechanical ventilation in the pediatric intensive care unit, to identify the key components of a music listening intervention and explore its mechanism of action, i.e., the biological pathway through which music listening decreases stress and pain.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Critical Illness
Keywords
mechanical ventilation, pain, stress, anxiety

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants will receive 3 conditions in a random order, via within-subject block randomization, each day for 3 consecutive days.
Masking
Outcomes Assessor
Masking Description
Study team members responsible for collecting data pre-post session will be masked to the condition received and condition order.
Allocation
Randomized
Enrollment
171 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Live music > Recorded music > Usual Care
Arm Type
Experimental
Arm Description
Order of conditions for the day
Arm Title
Recorded music > Usual care > Live music
Arm Type
Experimental
Arm Description
Order of conditions for the day
Arm Title
Usual Care > Live music > Recorded music
Arm Type
Experimental
Arm Description
Order of conditions for the day
Arm Title
Live music > Usual Care > Recorded music
Arm Type
Experimental
Arm Description
Order of conditions for the day
Arm Title
Recorded music > Live music > Usual care
Arm Type
Experimental
Arm Description
Order of conditions for the day
Arm Title
Usual care > Recorded music > Live music
Arm Type
Experimental
Arm Description
Order of conditions for the day
Intervention Type
Behavioral
Intervention Name(s)
Live music
Intervention Description
Live Music. A board-certified music therapist will provide live music (singing with instrument accompaniment) of child preferred songs, per caregiver report, with the tempo entrained to the child's respiratory rate at intervention start and decreased as needed to facilitate relaxation, with a target tempo of 60-80 beats per minute (BPM). Song choices will be based on patient preferences, per caregiver report, and performed with relaxing characteristics (steady rhythm and volume)
Intervention Type
Behavioral
Intervention Name(s)
Recorded music
Intervention Description
Recorded Music. MP3 players will be loaded with a recorded music playlist of the child's preferred songs, per caregiver report, and connected to two small speakers that are to be placed at either side of the head of the bed. Speakers will be tested with sound level meter and volume control set at 50-60 decibels. A member of the study team will stay at bedside throughout the recorded music condition. Study team member will log time of session and complete a checklist with open-response option to note relevant information (e.g., Session interruptions from other staff).
Intervention Type
Other
Intervention Name(s)
Usual care
Intervention Description
Usual Care. A pharmacologic approach to ameliorating stress and pain in MV children is standard of care in CHP's PICU. CHP provides weight-based guidelines to aid clinical decisions on medications for sedation and analgesia. Bedside nurses assess the child's sedation and pain scores once an hour and administered PRN medications as needed, based on clinical judgement, using CHP's PICU weight-based guidelines. For example, if a child has a pain score of >1-2 above goal, guidelines suggest providing a fentanyl dose of 0.5 mcg/kg and assessing again in 1 hour. We will include usual care as a third condition to explore how our selected biomarkers vary over 20 min. without the addition of any musical stimuli. A member of the study team will stay at bedside throughout the usual care condition. Study team member will log time of session and complete a checklist with open-response option to note relevant information (e.g., Session interruptions from other staff).
Primary Outcome Measure Information:
Title
Change in cortisol pre-post condition
Description
Percent change in saliva-based cortisol level, ng/ml. Reported as median change per condition and included as continuous outcome in linear regression.
Time Frame
Change from baseline to 30 min. and 60-90 min. post each condition for up to 3 days
Title
Change in Interleukin-6 (IL6) pre-post condition
Description
Percent change in saliva-based IL6 level, pg/ml. Reported as median change per condition and included as continuous outcome in linear regression.
Time Frame
Change from baseline to 30 min. and 60-90 min. post each condition for up to 3 days
Title
High Frequency (HF) Heart Rate Variability
Description
Trajectory of HF, a biomarker of sympathetic nervous activity. Reported as median value per condition and included as continuous outcome in linear regression.
Time Frame
1 hour prior through 2 hours post each condition, up to 3 days
Title
Low Frequency (LF) Heart Rate Variability
Description
Trajectory of LF, a biomarker of parasympathetic nervous activity. Reported as median value per condition and included as continuous outcome in linear regression.
Time Frame
1 hour prior through 2 hours post each condition, up to 3 days
Title
HF to LF ration (HF/LF) Heart Rate Variability
Description
Trajectory of HF/LF ratio, a biomarker of autonomic nervous system balance. Reported as median value per condition and included as continuous outcome in linear regression.
Time Frame
1 hour prior through 2 hours post each condition, up to 3 days
Title
Standard Deviation of Normal to Normal (SDNN) Heart Rate Variability
Description
Trajectory of SDNN, a biomarker of parasympathetic and sympathetic modulation
Time Frame
1 hour prior through 2 hours post each condition, up to 3 days
Secondary Outcome Measure Information:
Title
Acceptability
Description
Qualitative interviews with participants on intervention benefits, limitations, and optimizations. Reported as themes and sub-themes.
Time Frame
Interviews conducted within 2 weeks of completing primary data collection
Title
Change in Visual Analogue Scale of Anxiety
Description
Percent change in caregiver self-reported anxiety, scaled 0 [no anxiety] to 100 [extremely anxious]. Reported as median change per condition and included as continuous outcome in linear regression.
Time Frame
Change <30 min. pre-post each condition for up to 3 days
Title
Change in Face Legs Activity Consolability and Crying (FLACC)
Description
Percent change in observed pain, as measured by FLACC. Each of the 5 domains (e.g., Face, legs, etcs) is scored 0-2 and combined for a total score of 0 through 10, higher number indicates more pain. FLACC change score will be calculated from scores pre/post each condition. Reported as median change per condition and included as continuous outcome in linear regression.
Time Frame
Change <30 min. pre-post each condition for up to 3 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 5 -17 years old intubated and receiving MV expected to have a PICU stay of >72 hours Exclusion Criteria: Primary caregiver does not read, write, and speak English The child is not expected to survive the PICU stay The child has deafness in both ears, has a history of musicogenic epilepsy, is receiving neuromuscular blockade infusion The child has a diagnosis of COVID-19 The child was admitted for a new traumatic brain injury
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zachary Henry
Phone
4126927143
Email
zph7@pitt.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jessica M Jarvis, PhD
Organizational Affiliation
University of Pittsburgh
Official's Role
Principal Investigator
Facility Information:
Facility Name
UPMC Children's Hospital of Pittsburgh
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15224
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jessica M Jarvis, PhD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
23689789
Citation
Chlan LL, Weinert CR, Heiderscheit A, Tracy MF, Skaar DJ, Guttormson JL, Savik K. Effects of patient-directed music intervention on anxiety and sedative exposure in critically ill patients receiving mechanical ventilatory support: a randomized clinical trial. JAMA. 2013 Jun 12;309(22):2335-44. doi: 10.1001/jama.2013.5670.
Results Reference
background
PubMed Identifier
31652195
Citation
Liu MH, Zhu LH, Peng JX, Zhang XP, Xiao ZH, Liu QJ, Qiu J, Latour JM. Effect of Personalized Music Intervention in Mechanically Ventilated Children in the PICU: A Pilot Study. Pediatr Crit Care Med. 2020 Jan;21(1):e8-e14. doi: 10.1097/PCC.0000000000002159.
Results Reference
background
PubMed Identifier
34467386
Citation
Bush HI, LaGasse AB, Collier EH, Gettis MA, Walson K. Effect of Live Versus Recorded Music on Children Receiving Mechanical Ventilation and Sedation. Am J Crit Care. 2021 Sep 1;30(5):343-349. doi: 10.4037/ajcc2021646.
Results Reference
background

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Music Listening: A Mechanistic Trial

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