Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
68 participants
INTERVENTIONAL
2021-12-01
2022-02-01
Brief Summary
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Detailed Description
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The study is a randomized controlled study to determine the effect of white noise on sucking success and infant comfort in newborn babies between 34-37 weeks of gestation who were fed orally by a full enteral mother hospitalized in the Neonatal Intensive Care Unit.
Place and Time of the Study
The research was conducted in the Bulent Ecevit Training and Research Hospital Neonatal Intensive Care Unit between 01.09.2020 and 01.03.2021.
MATERIAL AND METHOD OF THE RESEARCH
The study is a randomized controlled study to determine the effect of white noise on sucking success and infant comfort in newborn babies between 34-37 weeks of gestation who were fed orally by a full enteral mother hospitalized in the Neonatal Intensive Care Unit.
Research Universe
The universe of the study consisted of newborn babies who were born in the Bulent Ecevit Training and Research Hospital Neonatal Intensive Care Unit between 01.09.2020 and 01.03.2021 and who met the inclusion criteria in the study and the babies who were fed by the mother who passed to the mother's room.
Research Sample Thirty control newborn infants who volunteered to participate in the study and met the inclusion criteria were formed by 30 newborns in the white noise group.
Sampling Selection Criteria
* Gestational age between 34-37 weeks,
* Having a birth weight of 1800-3600 g,
* Does not have any anatomical and physiological problems,
* Does not show any signs of disease and does not have any congenital disorder,
* Does not have a congenital or acquired malformation related to hearing
* Families without any disability to breastfeed
* Having parental consent
Materials and Methods
In this study, babies who were called to feed mothers who started to be fed orally with breast milk after leaving intensive care were selected. Informed consent form, Patient Identification Form and Application Registration Form, Premature Infant Comfort Scale, and LATCH Breastfeeding Diagnostic Measurement Tool were used for parents who accepted to participate in the study. The control group and the intervention group were first told about white noise and how it could affect breastfeeding, and the Informed Volunteer form, the Patient Identification Form and the Application Registration Form were filled. The mother and the baby were given the appropriate position and breastfeeding was initiated. No application was applied to the mother during the first breastfeeding. During the second breastfeeding, 30 neonatal groups were listened to the song "Your Baby Don't Cry" from Orhan OSMAN's album "Kolik". During the second breastfeeding, no music was played to the control group. After the procedure was completed, the data were collected by the researcher using the Premature Baby Comfort Scale, LATCH breastfeeding diagnostic measurement tool, Patient Diagnosis Form and Application Registration Form. Then the data will be analyzed in the spss 16.0 package program.
Data Collection Tools
* Introductory Information Form for Mother and Baby
* LATCH Breastfeeding Diagnostic Scale
* Premature Baby Comfort Scale Decibel measuring device
* Orhan Osman's Colic album-Don't Let Your Baby Cry II
Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
SINGLE
Study Groups
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music band
The starting person will first talk about white noise and explain how he can direct breastfeeding, and fill the Informed Volunteer Form, Patient Identification Form and Application Registration Form. The mother and baby will be given the appropriate position and breastfeeding will be started. No application will be applied to the mother during the first breastfeeding. During the second breastfeeding, 30 newborn group Orhan OSMAN's "Kolik" album will be played on the music player "Your Baby Don't Cry". After the process is completed, a written response will be received for the data Premature Baby Comfort Scale, LATCH breastfeeding diagnostic measurement tool, Patient Diagnosis Form and Application Registration Form.
Orhan OSMAN's track "Don't Let Your Baby Cry" in the "Kolik" album will be played on the music player.
white noise will be played while breastfeeding
control
First, the mother will be informed about the study. Then the appropriate position will be given. The informed volunteer form, the Patient Identification Form and the Application Registration Form will be filled. The mother and the baby will be given the appropriate position and breastfeeding will be started. No application will be applied to the mother during the first breastfeeding. No intervention will be applied during the second breastfeeding. After the procedure is completed, a written response will be received with the data Premature Infant Comfort Scale, LATCH breastfeeding diagnostic measurement tool, Patient Diagnosis Form and Application Registration Form.
No interventions assigned to this group
Interventions
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Orhan OSMAN's track "Don't Let Your Baby Cry" in the "Kolik" album will be played on the music player.
white noise will be played while breastfeeding
Eligibility Criteria
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Inclusion Criteria
* Does not have any anatomical and physiological problems,
* Does not show any signs of disease and does not have any congenital disorder,
* Does not have a congenital or acquired malformation related to hearing
* Families without any disability to breastfeed
* Having parental consent
Exclusion Criteria
* Birth weight not in the range of 1800-3600,
* Having any anatomical and physiological problems
* Any signs of illness and congenital disorder
* Having a congenital or acquired malformation related to hearing
* Families who have any disability to breastfeed
* No parental consent
34 Weeks
37 Weeks
ALL
Yes
Sponsors
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Esra Tanrıverdi
OTHER
Responsible Party
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Esra Tanrıverdi
Research Assistant
Locations
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Zonguldak Bülent Ecevit Eğitim Araştırma Research Hospital
Zonguldak, , Turkey (Türkiye)
Countries
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Other Identifiers
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12102020100153
Identifier Type: -
Identifier Source: org_study_id