- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01463176
Music Therapy as Procedural Support for Young Children Undergoing Immunizations
August 10, 2015 updated by: Florida State University
Music Therapy as Procedural Support for Young Children Undergoing Immunizations: A Randomized Controlled Study
Many young children undergo medical procedures that are painful and distressing.
Negative experiences during medical procedures can have serious long-term effects, including fear and avoidance of medical procedures during adulthood.
Distraction interventions can help prevent children from forming negative memories of medical procedures.
Live music therapy has been shown to alleviate pediatric distress during both invasive and non-invasive procedures.
The objective of this study is to examine the effects of music therapy on the child's distress behaviors and time to calm, as well as the length of the procedure and use of restraint, and parents' and healthcare staffs' behaviors during the procedure, for young children undergoing immunizations and influenza vaccinations.
It is hypothesized that children receiving music therapy will show fewer distress behaviors, calm more quickly, and have shorter procedures with fewer instances of restraint compared to children who receive standard care.
In addition, it is predicted that adults (parents and staff) will show fewer distress-promoting behaviors during, before, and after the procedures.
Study Overview
Study Type
Interventional
Enrollment (Actual)
150
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 Locations
-
-
Florida
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Tallahassee, Florida, United States, 32303
- Tallahassee Primary Care Associates
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Tallahassee, Florida, United States, 32308
- Tallahassee Memorial HealthCare Family Medicine Clinic
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Georgia
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Bainbridge, Georgia, United States, 39819
- Memorial Pediatrics
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-
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
4 years to 6 years (CHILD)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Participants will be pediatric patients (N = 60) from 48 to 72 months of age who are undergoing immunizations, as well as their parents/legal guardians (N = 60) and the healthcare staff who are conducting/assisting with their procedure (N = 60).
Exclusion Criteria:
- Any children whose parents are non-English speakers or staff who are non-English speakers will be excluded.
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: SUPPORTIVE_CARE
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
NO_INTERVENTION: Standard Care
Children in the Standard Care Control group will receive standard care and will be videotaped by the music therapist but will not receive music therapy during their immunization
|
|
|
EXPERIMENTAL: Music Therapy
Children in this group will receive live music therapy during their immunization.
|
Live music therapy is interactive and incorporates behavioral cues for coping techniques during the procedure, using patient-preferred music.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Child's behavioral distress, as measured by the Children's Hospital of Eastern Ontario Pain Scale (CHEOPS)
Time Frame: From the time the nurse enters the treatment room until the child leaves the treatment room after the procedure (approximately 5-10 minutes)
|
Distress will be assessed at fifteen second intervals throughout the procedure by trained observers upon review of videos of procedures (within approximately one month of procedure)
|
From the time the nurse enters the treatment room until the child leaves the treatment room after the procedure (approximately 5-10 minutes)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Child and adult behaviors, as measured by the Child-Adult Medical Procedure Interaction Scale- Short Form (CAMPIS-SF)
Time Frame: From the time the nurse enters the treatment room until the child leaves the treatment room after the procedure (approximately 5-10 minutes)
|
Child and adult behaviors will be assessed at fifteen second intervals throughout the procedure by trained observers upon review of videos of procedures (within approximately one month of procedure).
|
From the time the nurse enters the treatment room until the child leaves the treatment room after the procedure (approximately 5-10 minutes)
|
|
Child's pain and distress, reported by the child's parent using the Universal Pain Assessment Tool
Time Frame: After the procedure, when the child and parent have left the treatment room (within approximately 5 minutes of the procedure).
|
After the procedure, when the child and parent have left the treatment room (within approximately 5 minutes of the procedure).
|
|
|
Parent perceptions of and satisfaction with the procedure, measured using a researcher-designed satisfaction survey
Time Frame: After the procedure, when the child and parent have left the treatment room (within approximately 5 minutes of the procedure).
|
After the procedure, when the child and parent have left the treatment room (within approximately 5 minutes of the procedure).
|
|
|
Length of time it takes the child to calm after the procedure, in minutes and seconds
Time Frame: Observers will begin recording the length of time to calm starting with the needle insertion and ending when the child receives a CHEOPS score of 6 or less (within approximately 5 minutes after needle insertion).
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Assessed by trained observers upon review of a video tape of the procedure (within approximately a month of the procedure)
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Observers will begin recording the length of time to calm starting with the needle insertion and ending when the child receives a CHEOPS score of 6 or less (within approximately 5 minutes after needle insertion).
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Olivia S Yinger, MME, Florida State University
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
October 1, 2011
Primary Completion (ACTUAL)
August 1, 2012
Study Completion (ACTUAL)
August 1, 2012
Study Registration Dates
First Submitted
October 20, 2011
First Submitted That Met QC Criteria
October 28, 2011
First Posted (ESTIMATE)
November 1, 2011
Study Record Updates
Last Update Posted (ESTIMATE)
August 11, 2015
Last Update Submitted That Met QC Criteria
August 10, 2015
Last Verified
August 1, 2015
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2011.6797
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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