- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05967572
The Effect of Different Music Listened During Retinopathy Examination to Premature Infants
January 23, 2024 updated by: Semra Kose, Necmettin Erbakan University
The Effect of Different Music Listened During Retinopathy Examination to Premature Infants on Their Pain and Comfort Level: A Randomized Controlled Trial
Retinopathy of Prematurity (ROP); It is a disease of premature and low birth weight infants, characterized by incomplete vascularization of the retina, etiology and pathogenesis of which is unknown, and causes vision loss.
There is an increase in the incidence and severity of ROP development in direct proportion to the decrease in birth week and birth weight.
While ROP is a problem below 32 weeks of gestation in developed countries, it is reported to develop severely up to 34 weeks of gestation in developing countries.
In a multicenter study conducted by the Turkish Neonatology Society in our country, the frequency of ROP in very low birth weight preterm infants was found to be 42%, and the frequency of advanced ROP was 11%.
The incidence of ROP in babies with a gestational age of 33-35 weeks was 6.1%, and advanced ROP was 6 per thousand.
The frequency of ROP was found to be 10.3% in babies with a birth weight of 1500-2000 grams, and severe ROP was reported in 19 of these babies.
ROP examination is a procedure that causes pain, deterioration in comfort and physiological changes in preterm newborns.
After this examination, an increase in blood pressure and heart rate and a decrease in oxygen saturation are observed.
Pharmacological and non-pharmacological (non-pharmacological) methods are used to reduce the pain and increase the comfort level of the premature newborn.
As a pharmacological method, there is no other routine method used to reduce pain other than the administration of local anesthetic drops before the examination.
Because of this situation, nurses apply various non-pharmacological methods to alleviate pain.
These methods are; breast milk, sucrose use, oral dextrose use, non-nutritive sucking, positioning, listening to music and mother's voice.
In the literature, no specific study was found in which music was used to reduce pain and increase the comfort level during the ROP examination.
Therefore, this research will be carried out to determine the effect of different music played on the pain and comfort level of premature babies during the retinopathy examination.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Retinopathy of Prematurity (ROP); It is a disease characterized by incomplete vascularization of the retina seen in premature and low birth weight infants, the etiology and pathogenesis of which are unknown, causing vision loss.
There is an increase in the incidence and severity of ROP development in direct proportion to the decrease in the week of birth and birth weight.
While ROP is a problem below 32 weeks of gestation in developed countries, it is reported to develop severely up to 34 weeks of gestation in developing countries.
In a multicenter study conducted by the Turkish Neonatology Society in our country, the frequency of ROP in very low birth weight preterm infants was found to be 42%, and the frequency of advanced ROP was 11%.
The incidence of ROP in babies with a gestational age of 33-35 weeks was 6.1%, and advanced ROP was 6 per thousand.
The frequency of ROP was found to be 10.3% in babies with a birth weight of 1500-2000 grams, and severe ROP was reported in 19 of these babies.
Thanks to the increasing frequency of preterm birth in recent years and scientific and technological advances in neonatology, life expectancy is extended up to the 23rd week of gestation.
However, this increased the incidence of retinopathy.
Therefore, it is of great importance for neotologists, pediatricians and nurses who care for preterms to know the pathophysiology, staging, risk factors and principles of appropriate care for them in reducing the incidence, possible complications and mortality rates of ROP.
ROP examination is a procedure that causes pain, deterioration in comfort and physiological changes in preterm newborns.
After this examination, an increase in blood pressure and heart rate and a decrease in oxygen saturation are observed.
These physiological changes observed after the examination continue for 24 hours.
Pharmacological and non-pharmacological (non-pharmacological) methods are used to reduce the pain and increase the comfort level of the premature newborn.
As a pharmacological method, there is no other routine method used to reduce pain other than the administration of local anesthetic drops before the examination.
Because of this situation, nurses apply various non-pharmacological methods to alleviate pain.
These methods are; breast milk, sucrose use, oral dextrose use, non-nutritive sucking, positioning, listening to music and mother's voice.
In the literature review; In a study evaluating the effectiveness of sucrose combination with non-nutritive sucking, they reported that pain was moderately reduced and more studies are needed.
In another study (2015), it was concluded that topical anesthesia and oral dextrose were not effective in reducing pain in both groups.
In a study comparing the effectiveness of breast milk and sucrose, it is recommended to use breast milk because of the rapid recovery of the baby after the ROP examination.
In the comparison of the position, which is another non-pharmacological method, with the routine practice in the study conducted in 2019; It has been concluded that the frock position is more effective in relieving pain.
In another study, it was stated that the mother's voice as music therapy also showed an analgesic effect and accelerated the recovery after the ROP examination.
In the light of this information, when we look at the literature, no specific study was found in which a rain stick and The Happiest Baby music were used to reduce pain and increase the comfort level during the ROP examination.
Therefore, this research will be carried out to determine the effect of different music played on the pain and comfort level of premature babies during the retinopathy examination.
Study Type
Interventional
Enrollment (Estimated)
84
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: Semra KÖSE, PhD, Asisstant Proffessor
- Phone Number: 05433682203
- Email: semraak_88@hotmail.com
Study Contact Backup
- Name: Gizem Kıvrak
- Email: gizemynlc@gmail.conm
Study Locations
-
-
Meram
-
Konya, Meram, Turkey
- Recruiting
- Necmettin Erbakan University
-
Contact:
- Semra KÖSE, PhD, Assistant Proffessor
-
-
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
- Child
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
• Gestational age ≤34 weeks
- Birth Weight ≤2000 grams
- Preterm newborns with a corrected/postnatal age of 28-36 weeks at the time of examination
- Having the baby's first ROP examination
- Not giving sedative, opioid and anticonvulsant drugs before/during the examination
- Parents do not have diagnosed mental or mental problems and agree to participate in the research.
Exclusion Criteria:
Presence of a condition that prevents pain assessment (intracranial hemorrhage, neuromotor developmental retardation, etc.)
- Oxygen requirement (nasal cannula, hood or incubator)
- Having any congenital defect (eye, neurological) that may adversely affect the examination
- Having a diagnosed hearing loss
- Performing a different painful procedure at least one hour before the ROP
- Being connected to a mechanical ventilator
- Congenital hearing problems in family members
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 Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experiment 1 (Rainstick)
The experimental group will start playing music 3 minutes before the start of the process.
The examination begins with the insertion of the speculum into the eye.
The duration of the examination depends on the visibility of the vascularity in the retina and the examination will end with the removal of the speculum from the eye.
The rain bar will continue to play during the ROP inspection.
The rain stick will be played 25cm away from the baby.
|
|
|
Experimental: Experiment 2 (Music-The Happiest Baby)
During the ROP examination, Dr. Harvery Karp's "The Happiest Baby", which consists of only intrauterine sounds, is a group of babies who are listened to.
The experimental group will start playing music 3 minutes before the start of the process.
The examination begins with the insertion of the speculum into the eye.
The duration of the examination depends on the visibility of the vascularity in the retina and the examination will end with the removal of the speculum from the eye.
Music will continue to play during the ROP exam.
The voice recorder that will play The Happiest Baby will be placed 25 cm away from the baby.
In the study, the music volume will be set as 45-50 decibels.
|
|
|
No Intervention: Control
It is the group of infants who receive routine care during the ROP examination.
In the control group, a routine ROP procedure will be performed without any music before, during and after the ROP examination.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Baby Information Form:
Time Frame: It will be applied when babies first arrive.
|
This form consists of 6 questions including the baby's birth weight, birth week, current weight, corrected week, and delivery type.
|
It will be applied when babies first arrive.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Premature Infant Pain Profile (PIPP)
Time Frame: Approximately 2 minutes of video will be recorded and measurement will be taken approximately in the first minute of the video and 2 minutes after the video.
|
Pain assessment of preterm infants was performed with Premature Infant Pain Profile.
The scale, which was developed by Stevens et al. in 1996 for 28-36 weeks preterms, is a multidimensional measurement tool with 7 sub-title evaluation criteria in the evaluation of acute pain in preterms (Gibbins et al., 2014).
Turkish validity and reliability for all term and preterms were made by Derebent in 2007 within the scope of his master's thesis (Derebent, 2007).
All sub-headings are scored between 0,1,2,3.
According to the Turkish validity and reliability study of the scale, the highest score obtained from the scale is 21; 0-6 points indicate mild pain, 7-12 points indicate moderate pain, and 13-21 points indicate severe pain.
|
Approximately 2 minutes of video will be recorded and measurement will be taken approximately in the first minute of the video and 2 minutes after the video.
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Premature Baby Comfort Scale
Time Frame: Approximately 2 minutes of video will be recorded and measurement will be taken approximately in the first minute of the video and 2 minutes after the video.
|
Ambuel et al.
The comfort scale was developed by Monique et al.
This scale was adapted to Turkish by Alemdar and Tüfekçi in 2015 by Alemdar and Tüfekçi.
PBKO; It is a multidimensional scale used to evaluate behavioral and psychological comfort and pain.
PBCS assesses 7 parameters such as Alertness, Calmness/Agitation, Respiratory Status (only with mechanical ventilation support) or Crying (not evaluated because it is scored only in children with spontaneous breathing), Physical Movement, Muscle Tone, Facial Movements, and Average Heart Rate.
Accordingly, 35 indicates the lowest comfort score and 7 the highest.
A high score on the scale indicates a low level of comfort.
If the total score obtained is ≥17, it is the cut-off value of the scale, the limit value for the infant's comfort level, and indicates the need for an intervention to reduce pain.
|
Approximately 2 minutes of video will be recorded and measurement will be taken approximately in the first minute of the video and 2 minutes after the video.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Semra KÖSE, Necmettin Erbakan University
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
- Bilgeç, G. H., & Erol N. (2018). Epidemiology, Prevalence and Incidence in Retinopathy of Prematurity (Vol. 2, Issue 1). Chen, H. L., Chen, C. H., Wu, C. C., Huang, H. J., Wang, T. M., & Hsu, C. C. (2009). The Influence of Neonatal Intensive Care Unit Design on Sound Level. Pediatrics and Neonatology, 50(6), 270-274. https://doi.org/10.1016/S1875-9572(09)60076-0 Cohen, J. (2013). Statistical power analysis for the behavioral sciences. Routledge. Corrigan, M. J., Keeler, J. R., Miller, H. D., ben Khallouq, B. A., & Fowler, S. B. (2020). Music therapy and retinopathy of prematurity screening: using recorded maternal singing and heartbeat for post exam recovery. Journal of Perinatology, 40(12), 1780-1788. https://doi.org/10.1038/S41372-020-0719-9 Derebent, E. (2007). The Effect of Kangaroo Care on Reducing Pain During Invasive Procedures for Premature Babies. Dilli, D., Ilarslan, N. E. Ç., Kabataş, E. U., Zenciroǧlu, A., Şimşek, Y., & Okumuş, N. (2014). Oral sucrose and non-nutritive sucking goes some way to reducing pain during retinopathy of prematurity eye examinations. Acta Paediatrica (Oslo, Norway: 1992), 103(2). https://doi.org/10.1111/APA.12454 Dolgun, G. (2019). The Use of Pulse Oximetry in Defining Critical Congenital Heart Diseases and the Role of Midwife-Nurse. Journal of Education and Research in Nursing. https://doi.org/10.5222/head.2019.134 Gibbins, S., Stevens, B. J., Yamada, J., Dionne, K., Campbell-Yeo, M., Lee, G., Caddell, K., Johnston, C., & Taddio, A. (2014). Validation of the Premature Infant Pain Profile-Revised (PIPP-R). Early Human Development, 90(4), 189-193. https://doi.org/10.1016/J.EARLHUMDEV.2014.01.005 Koç, E., Yağmur, A., Prof, B., Özdek, S., & Ovali, F. (2021). Turkish Neonatology Society Turkish Ophthalmology Society Turkey Retinopathy of Prematurity Guideline 2021 Update. Küçük Alemdar, D., & Güdücü Tüfekci, F. (2015). The Reliability and Validity of the Premature Infant Comfort Scale's Turkish. Journal of Education and Research in Nursing. https://doi.org/10.5222/head.2015.142 Metres, O. (2014). Retinopathy of Prematurity from a Nursing Perspective. https://cms.galenos.com.tr/Uploads/Article_25271/European%20Archives%20of%20Medical%20Research-30-63-En.pdf Metreş, Ö., & Yıldız, S. (2019). Pain Management with ROP Position in Turkish Preterm Infants During Eye Examinations: A Randomized Controlled Trial. Journal of Pediatric Nursing, 49, e81-e89. https://doi.org/10.1016/J.PEDN.2019.08.013 Nesargi, S. v, Nithyanandam, S., Rao, S., Nimbalkar, S., & Bhat, S. (2015). Topical Anesthesia or Oral Dextrose for the Relief of Pain in Screening for Retinopathy of Prematurity: a Randomized Controlled Double-blinded Trial. https://doi.org/10.1093/tropej/fmu058 Parra, J., de Suremain, A., Berne Audeoud, F., Ego, A., & Debillon, T. (2017). Sound levels in a neonatal intensive care unit significantly exceeded recommendations, especially inside incubators. Acta Paediatrica, International Journal of Paediatrics, 106(12), 1909-1914. https://doi.org/10.1111/apa.13906 Sancak, S., Topçuoğlu, S., Çelik, G., Günay, M., & Karatekin, G. (2019). Frequency of Retinopathy of Prematurity and Evaluation of Risk Factors. Zeynep Kamil Medical Bulletin. https://doi.org/10.16948/zktipb.474762 Sun, X., Lemyre, B., Barrowman, N., & O'Connor, M. (2010). Pain management during eye examinations for retinopathy of prematurity in preterm infants: A systematic review. In Acta Paediatrica, International Journal of Paediatrics (Vol. 99, Issue 3, pp. 329-334). https://doi.org/10.1111/j.1651-2227.2009.01612.x Şener Taplak, A., & Erdem, E. (2017). A Comparison of Breast Milk and Sucrose in Reducing Neonatal Pain During Eye Exam for Retinopathy of Prematurity. Breastfeeding Medicine: The Official Journal of the Academy of Breastfeeding Medicine, 12(5), 305-310. https://doi.org/10.1089/BFM.2016.0122 Taplak, A. S., & Erdem, E. (2018). Pain Management in Examination for Retinopathy of Prematurity. In Journal of Health Sciences) (Vol. 27, Issue 2).
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)
June 1, 2023
Primary Completion (Estimated)
March 1, 2024
Study Completion (Estimated)
July 1, 2024
Study Registration Dates
First Submitted
July 8, 2023
First Submitted That Met QC Criteria
July 21, 2023
First Posted (Actual)
August 1, 2023
Study Record Updates
Last Update Posted (Estimated)
January 24, 2024
Last Update Submitted That Met QC Criteria
January 23, 2024
Last Verified
January 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- NecmettinEUSKose
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
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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