- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05541029
Music Listening: A Mechanistic Trial
January 16, 2026 updated by: Jessica Jarvis, University of Pittsburgh
Music Listening Interventions for Children Receiving Mechanical Ventilation: A Mechanistic Trial
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.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
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.
Study Type
Interventional
Enrollment (Estimated)
171
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Jessica Eldridge
- Phone Number: 4126927143
- Email: eldridgejl@upmc.edu
Study Locations
-
-
Pennsylvania
-
Pittsburgh, Pennsylvania, United States, 15224
- Recruiting
- UPMC Children's Hospital of Pittsburgh
-
Contact:
- Jessica M Jarvis, PhD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
5 years to 17 years (Child)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- 2 months -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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Live music > Recorded music > Usual Care
Order of conditions for the day
|
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)
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).
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).
|
|
Experimental: Recorded music > Usual care > Live music
Order of conditions for the day
|
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)
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).
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).
|
|
Experimental: Usual Care > Live music > Recorded music
Order of conditions for the day
|
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)
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).
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).
|
|
Experimental: Live music > Usual Care > Recorded music
Order of conditions for the day
|
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)
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).
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).
|
|
Experimental: Recorded music > Live music > Usual care
Order of conditions for the day
|
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)
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).
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).
|
|
Experimental: Usual care > Recorded music > Live music
Order of conditions for the day
|
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)
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).
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).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in cortisol pre-post condition
Time Frame: Change from baseline to 30 min. and 60-90 min. post each condition for up to 3 days
|
Percent change in saliva-based cortisol level, ng/ml.
Reported as median change per condition and included as continuous outcome in linear regression.
|
Change from baseline to 30 min. and 60-90 min. post each condition for up to 3 days
|
|
Change in Interleukin-6 (IL6) pre-post condition
Time Frame: Change from baseline to 30 min. and 60-90 min. post each condition for up to 3 days
|
Percent change in saliva-based IL6 level, pg/ml.
Reported as median change per condition and included as continuous outcome in linear regression.
|
Change from baseline to 30 min. and 60-90 min. post each condition for up to 3 days
|
|
High Frequency (HF) Heart Rate Variability
Time Frame: 1 hour prior through 2 hours post each condition, up to 3 days
|
Trajectory of HF, a biomarker of sympathetic nervous activity.
Reported as median value per condition and included as continuous outcome in linear regression.
|
1 hour prior through 2 hours post each condition, up to 3 days
|
|
Low Frequency (LF) Heart Rate Variability
Time Frame: 1 hour prior through 2 hours post each condition, up to 3 days
|
Trajectory of LF, a biomarker of parasympathetic nervous activity.
Reported as median value per condition and included as continuous outcome in linear regression.
|
1 hour prior through 2 hours post each condition, up to 3 days
|
|
HF to LF ration (HF/LF) Heart Rate Variability
Time Frame: 1 hour prior through 2 hours post each condition, up to 3 days
|
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.
|
1 hour prior through 2 hours post each condition, up to 3 days
|
|
Standard Deviation of Normal to Normal (SDNN) Heart Rate Variability
Time Frame: 1 hour prior through 2 hours post each condition, up to 3 days
|
Trajectory of SDNN, a biomarker of parasympathetic and sympathetic modulation
|
1 hour prior through 2 hours post each condition, up to 3 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Visual Analogue Scale of Anxiety
Time Frame: Change <30 min. pre-post each condition for up to 3 days
|
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 <30 min. pre-post each condition for up to 3 days
|
|
Change in Face Legs Activity Consolability and Crying (FLACC)
Time Frame: Change <30 min. pre-post each condition for up to 3 days
|
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.
|
Change <30 min. pre-post each condition for up to 3 days
|
|
Acceptability
Time Frame: Interviews conducted within 1 month of completing primary data collection
|
Qualitative interviews with participants on intervention benefits, limitations, and optimizations.
Reported as themes and sub-themes.
|
Interviews conducted within 1 month of completing primary data collection
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Jessica M Jarvis, PhD, University of Pittsburgh
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- 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.
- 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.
- 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.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 20, 2023
Primary Completion (Estimated)
April 8, 2027
Study Completion (Estimated)
May 3, 2027
Study Registration Dates
First Submitted
September 12, 2022
First Submitted That Met QC Criteria
September 12, 2022
First Posted (Actual)
September 15, 2022
Study Record Updates
Last Update Posted (Actual)
January 20, 2026
Last Update Submitted That Met QC Criteria
January 16, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- STUDY22080069
- K23HD106011 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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