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CompletedNCT05263973Updated Oct 12, 2023

The Effect of Music on Pain, Comfort and Physiological Parameters During Prematurity Retinopathy Examination

An interventional study of Music in ROP Examination, sponsored by TC Erciyes University. Completed at 1 site in Turkey. Open to participants aged Up to 32 Weeks, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-10-12.

Sponsored by TC Erciyes University · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
28
Allocation
Randomized
Ages
Up to 32 Weeks
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • ROP Examination

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03

In context

Premature Birth

2,554 studies on the registry are indexed under Premature Birth; 498 are open to participants now.

This study's enrollment of 28 is below the median of 84 across 1,689 interventional studies indexed under Premature Birth.

Browse Premature Birth studies →

Lead sponsor

TC Erciyes University is the lead sponsor of 341 studies on the registry; 76 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Up to 32 Weeks
Sexes eligible
All
Accepts healthy volunteers
Yes

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

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.
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
28 participants (actual)

Study arms

  • Experimental
    Music group

    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.

    Other: Music

  • No intervention
    No intervention

    The infants in the control group will not be subjected to any intervention other than their clinical routines, only observation will be made.

Interventions

  • OtherMusic

    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

06

What researchers measure

Primary outcomes

  1. 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.

    Time frame: The measurement will start 4 minutes before the ROP examination and will end 4 minutes after the ROP examination.

  2. 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.

    Time frame: The measurement will start 4 minutes before the ROP examination and will end 4 minutes after the ROP examination.

  3. Physiological parameters- heart rate

    Heart rate

    Time frame: The measurement will start 4 minutes before the ROP examination and will end 4 minutes after the ROP examination.

  4. Physiological parameters- oxygen saturation

    Oxygen saturation

    Time frame: The measurement will start 4 minutes before the ROP examination and will end 4 minutes after the ROP examination.

  5. Physiological parameters- respiratory rate

    Respiratory rate

    Time frame: The measurement will start 4 minutes before the ROP examination and will end 4 minutes after the ROP examination.

  6. Physiological parameters- crying time

    Crying time

    Time frame: immediately after the ROP examination.

07

Study locations

1 site
  • Erciyes university
    Kayseri, Turkey
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 12, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05263973
Lead sponsor
TC Erciyes University
Responsible party
Yağmur Sezer Efe (Assist. Prof. Yağmur Sezer Efe, TC Erciyes University) — Principal investigator
First posted
Mar 3, 2022
Start date
Mar 10, 2022
Primary completion
Jan 10, 2023
Completion
Jan 10, 2023
Last update
Oct 12, 2023

Study contacts

Yağmur Sezer Efe, Assist. Prof.
principal investigator · TC Erciyes University

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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