The Effect of Music on Pain, Comfort and Physiological Parameters During Prematurity Retinopathy Examination
Primary Purpose
ROP Examination
Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Music
Sponsored by

About this trial
This is an interventional supportive care trial for ROP Examination
Eligibility Criteria
Inclusion Criteria:
- Birth weight <2000 g,
- Gestational age ≤32 weeks,
- Have not passed the first 2 ROP inspections,
- Not receiving ventilatory support (not intubated or positive pressure ventilation support) for the last 72 hours,
- Vital signs within normal limits (without tachycardia, tachypnea, hyperthermia, hypothermia, dyspnea, intercostal or subcostal retraction),
- Not having any congenital anomalies (eye, neurological) that may adversely affect the examination,
- No hearing problem,
- No painful intervention is performed at least 30 minutes before the ROP examination,
- Preterm newborns whose corrected/postnatal age is 28-36 weeks at the time of examination,
- Newborns whose mothers want to participate in the study will be included in the study.
Exclusion Criteria:
- Clinic condition worsening during working,
- Diagnosed with hydrocephalus, necrotizing enterocolitis, indirect hyperbilirubinemia,
- Receiving analgesic treatment,
- Newborns whose mothers want to withdraw from the study will be excluded from the study groups.
Sites / Locations
- Erciyes university
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Music group
No intervention
Arm Description
The infants in the music group (Acem Aşiran Maqam music prepared by TÜMATA group) will be applied music for a about total of 12 minutes, starting 3 minutes before the ROP examination and continuing during the ROP examination, 3 minutes after ROP examination.
The infants in the control group will not be subjected to any intervention other than their clinical routines, only observation will be made.
Outcomes
Primary Outcome Measures
Premature Infant Comfort Scale (PBIC)
According to the PICS, a score between 7-35 is obtained from the scale. A high score from the scale indicates a low level of comfort.
Premature Baby Pain Profile Scale-Revised Form (PIPP-R)
The PIPP-R is a Likert-type scale. In scoring the scale, items related to physiological and behavioral elements are scored as 0, 1, 2, 3, reflecting the difference between the values at baseline and during the procedure in each variable. Contextual items (behavioral status and CI) are scored as 3, 2, 1, 0 only at the beginning of the pain assessment (before touching the baby). According to the PIPP-R, the baby's pain is evaluated over the total score. Accordingly, the highest score that can be obtained from the PIPP-R scale for preterm newborns is 21 and 18 for term newborns.
Physiological parameters- heart rate
Heart rate
Physiological parameters- oxygen saturation
Oxygen saturation
Physiological parameters- respiratory rate
Respiratory rate
Physiological parameters- crying time
Crying time
Secondary Outcome Measures
Full Information
NCT ID
NCT05263973
First Posted
February 22, 2022
Last Updated
October 10, 2023
Sponsor
TC Erciyes University
1. Study Identification
Unique Protocol Identification Number
NCT05263973
Brief Title
The Effect of Music on Pain, Comfort and Physiological Parameters During Prematurity Retinopathy Examination
Official Title
The Effect of Music on Pain, Comfort and Physiological Parameters During Prematurity: A Randomized Controlled Study
Study Type
Interventional
2. Study Status
Record Verification Date
October 2023
Overall Recruitment Status
Completed
Study Start Date
March 10, 2022 (Actual)
Primary Completion Date
January 10, 2023 (Actual)
Study Completion Date
January 10, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
TC Erciyes University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
It is planned to determine the effect of music during Retinopathy of Prematurity (ROP) examination on pain, comfort and physiological parameters in preterm infants. This is single-center, randomized controlled trial, double blind, parallel.
Hypotheses:
H1: The music applied during the ROP examination has an effect on the Revised Premature Infant Pain Profile (PIPP-R) score of the preterm infant.
H2: The music applied during the ROP examination has an effect on the Preterm Infant Comfort Scale (PMI) score of the preterm infant.
H3: Music applied during the ROP examination has an effect on the physiological parameters (peak heart rate, O2 saturation) of the preterm infant.
H4: The music applied during the ROP examination has an effect on the crying time of the preterm infant during the procedure.
Method: The study will be performed with preterm infants (n=28) hospitalized in the neonatal intensive care unit of a tertiary hospital. Premature infants to be included in the study will be assigned to two study groups using the block randomization method created in the computer environment according to their gestational age, gender, birth weight.
The data in the study were will be collected using the Questionaire Form for Preterm Newborns and Their Parents, Physiological Parameters Observation Form, Revised-Premature Infant Pain Profile (PIPP-R), Premature Infant Comfort Scale (PICS), Pulse Oximeter, Music CD, Music box, Video camera, decibel meter, tripod. Data will be collected by researcher ABÇ. Infants who meet the criteria for inclusion in the study will be selected from the infants who are planned to an ROP examination, and written and verbal consent will be obtained from the families by explaining the purpose of the study.
Questionaire Form for Preterm Newborns and Their Parents will be obtained from the nurse observation form and patient files. Four minutes before the ROP, the infant will be monitored and physiological parameters will be recorded, and three minutes before the ROP, the experimental group will start to listen to music (Video recordings will be evaluated by three experts, PIPP-R and PICS). The music recording will continue to be played during the ROP examination for music group. No application will be made for the control group other than the clinical routines.
Detailed Description
This randomized controlled experimental study is planned in order to determine the effect of music on pain, comfort and physiological parameters in preterm infants in ROP examination matched for gestational age, gender and birth weight. The research sample will consist of 28 preterm infants who meet the inclusion criteria. In the literature, the number of infants varies between 10 and 30 in different studies in which music was applied to preterm infants. In this study, it was decided that the number of infants in the groups should be 14 according to α=95% confidence level and 90% power. In the study, it was planned to have 14 infants in the music and control groups. After reaching 28 preterm infants in the study, power analysis will be calculated using pain scores and it will be decided whether the sample size is sufficient or not. All bodies of preterm infants will be recorded with a visible video camera for an average of 10 minutes, 4 minutes before the start of the ROP examination and 4 minutes after the completion of the ROP examination (for PIPP-R and PICS scores). The infants in the music group (Acem Aşiran Maqam music prepared by TÜMATA group) will be applied music for a about total of 10 minutes, starting 3 minutes before the ROP examination and continuing during the ROP examination, 3 minutes after ROP examination. After the necessary disinfection process is done, the voice recorder will be placed in the incubator at a distance of 45 cm from the head of infant and the sound level will be adjusted to an average of 45-60 decibels. The examination will begin with the placement of the speculum in the eye. The duration of the examination varies according to the visibility of the retinal vascularity, and the examination will end with the removal of the speculum from the eye (mean ROP time 1.61 ±1.59). The infants in the control group will not be subjected to any intervention other than their clinical routines, only observation will be made. Data will be collected with the Questionaire Form for Preterm Newborns and Their Parents, Physiological Parameters Observation Form, Revised-Premature Infant Pain Profile (PIPP-R), Premature Infant Comfort Scale (PICS), Pulse Oximeter, Music CD, Music box, Video camera, decibel meter, tripod.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
ROP Examination
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Music
Masking
ParticipantOutcomes Assessor
Masking Description
Double (Participant, Outcomes Assessor)
Allocation
Randomized
Enrollment
28 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Music group
Arm Type
Experimental
Arm Description
The infants in the music group (Acem Aşiran Maqam music prepared by TÜMATA group) will be applied music for a about total of 12 minutes, starting 3 minutes before the ROP examination and continuing during the ROP examination, 3 minutes after ROP examination.
Arm Title
No intervention
Arm Type
No Intervention
Arm Description
The infants in the control group will not be subjected to any intervention other than their clinical routines, only observation will be made.
Intervention Type
Other
Intervention Name(s)
Music
Intervention Description
The infants in the music group (Acem Aşiran Maqam music prepared by TÜMATA group) will be applied music for a about total of 12 minutes, starting 3 minutes before the ROP examination and continuing during the ROP examination, 3 minutes after ROP examination
Primary Outcome Measure Information:
Title
Premature Infant Comfort Scale (PBIC)
Description
According to the PICS, a score between 7-35 is obtained from the scale. A high score from the scale indicates a low level of comfort.
Time Frame
The measurement will start 4 minutes before the ROP examination and will end 4 minutes after the ROP examination.
Title
Premature Baby Pain Profile Scale-Revised Form (PIPP-R)
Description
The PIPP-R is a Likert-type scale. In scoring the scale, items related to physiological and behavioral elements are scored as 0, 1, 2, 3, reflecting the difference between the values at baseline and during the procedure in each variable. Contextual items (behavioral status and CI) are scored as 3, 2, 1, 0 only at the beginning of the pain assessment (before touching the baby). According to the PIPP-R, the baby's pain is evaluated over the total score. Accordingly, the highest score that can be obtained from the PIPP-R scale for preterm newborns is 21 and 18 for term newborns.
Time Frame
The measurement will start 4 minutes before the ROP examination and will end 4 minutes after the ROP examination.
Title
Physiological parameters- heart rate
Description
Heart rate
Time Frame
The measurement will start 4 minutes before the ROP examination and will end 4 minutes after the ROP examination.
Title
Physiological parameters- oxygen saturation
Description
Oxygen saturation
Time Frame
The measurement will start 4 minutes before the ROP examination and will end 4 minutes after the ROP examination.
Title
Physiological parameters- respiratory rate
Description
Respiratory rate
Time Frame
The measurement will start 4 minutes before the ROP examination and will end 4 minutes after the ROP examination.
Title
Physiological parameters- crying time
Description
Crying time
Time Frame
immediately after the ROP examination.
10. Eligibility
Sex
All
Maximum Age & Unit of Time
32 Weeks
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Birth weight <2000 g,
Gestational age ≤32 weeks,
Have not passed the first 2 ROP inspections,
Not receiving ventilatory support (not intubated or positive pressure ventilation support) for the last 72 hours,
Vital signs within normal limits (without tachycardia, tachypnea, hyperthermia, hypothermia, dyspnea, intercostal or subcostal retraction),
Not having any congenital anomalies (eye, neurological) that may adversely affect the examination,
No hearing problem,
No painful intervention is performed at least 30 minutes before the ROP examination,
Preterm newborns whose corrected/postnatal age is 28-36 weeks at the time of examination,
Newborns whose mothers want to participate in the study will be included in the study.
Exclusion Criteria:
Clinic condition worsening during working,
Diagnosed with hydrocephalus, necrotizing enterocolitis, indirect hyperbilirubinemia,
Receiving analgesic treatment,
Newborns whose mothers want to withdraw from the study will be excluded from the study groups.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yağmur Sezer Efe, Assist. Prof.
Organizational Affiliation
TC Erciyes University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Erciyes university
City
Kayseri
Country
Turkey
12. IPD Sharing Statement
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The Effect of Music on Pain, Comfort and Physiological Parameters During Prematurity Retinopathy Examination
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