Non-Nutritive Sucking vs Non-Nutritive Sucking Combined With Breast Milk on the Neonatal Comfort
Study Details
Study Description
Brief Summary
The aim of the study is to determine the effect of the use of non-nutritive sucking vs non-nutritive sucking combined with breast milk on neonatal comfort during diaper change in preterm infants.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
Newborns are faced with many painful interventions including tactile stimulation such as diaper change, axillary temperature measurement, intraoral and endotracheal aspiration during the postnatal period in the Neonatal Intensive Care Units (NICU) at the beginning of their lives. Painful interventions negatively affect the physiological parameters, comfort, sleep, growth and hospital stay of newborns. As a result of these interventions, the stress level increases in preterm infants. Increased stress level can cause long-term sequelae, risk of intraventricular hemorrhage, increased oxygen consumption and hypertension. In addition, the increased stress experience may make the infant sensitive to pain and stress in other periods of his life.
This randomized controlled prospective study was planned to be conducted in the NICU of a private hospital with branches in Istanbul until the whole sample group would be reached.
In the NICU, where the study will be conducted, preterm infants will be divided into two groups as control and experimental groups. Non-nutritive sucking (NNS) combined with breast milk will be used during diaper change for newborns in the experimental group, and only NNS will be used in the control group. NNS will be given to both groups 5 minutes before diaper change. The comfort level of the newborns will be measured with the Premature Infant Comfort Scale before the NNS, 5 minutes after the NNS, during the procedure, immediately after the procedure and 5 minutes after the procedure.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Control group (Only NNS) NNS will be started 5 minutes before diaper change. The use of NNS will continue during diaper change and up to 5 minutes after the application. |
Procedure: Only NNS
Before the procedure, the Premature Infant Comfort Scale shall be filled out.
Procedure steps for the control group:
Materials shall be prepared (napkins, non-sterile gloves, pacifier)
Hands shall be washed; gloves shall be worn.
The infant shall be given a NNS just before the procedure and continue until the 5th minute after the procedure.
The diapers shall be changed.
Hands shall be washed after the procedure.
The Premature Infant Comfort Scale shall be assessed during, shortly after, and 5 minutes after the procedure.
|
| Experimental: Experimental Group (NNS Combined with Breast Milk) NNS combined with breast milk will be started 5 minutes before diaper change. The use of NNS combined with breast milk will continue during diaper change and up to 5 minutes after the application. |
Procedure: NNS Combined with Breast Milk
Before the procedure, the Premature Infant Comfort Scale shall be filled out.
Materials shall be prepared (napkins, non-sterile gloves, pacifier, breast milk, cup)
Hands shall be washed; gloves shall be worn.
The cylindrical part of a pacifier shall be in touch with breast milk for 5 seconds. The infant shall be given the pacifier, combined with breast milk, just before the procedure and continue until the 5th minute after the procedure.
The diapers shall be changed.
Hands shall be washed after the procedure.
The Premature Infant Comfort Scale shall be assessed during, shortly after, and 5 minutes after the procedure.
|
Outcome Measures
Primary Outcome Measures
- Change in Comfort Level [5 minutes before, immediately before, during, immediately after, and 5 minutes after the procedure.The change in these time intervals will be assessed.]
Infant's comfort level is evaluated with Premature Infant Comfort Scale.Premature Infant Comfort Scale (PICS), which is a multidimensional scale used in evaluating comfort and pain behaviorally and psychologically. The lowest score obtained from the scale is 35, and the highest score is 7. A high score on the scale indicates a low level of comfort.
Eligibility Criteria
Criteria
Inclusion Criteria:
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The preterm infants whose parents agree to participate in the research and sign the informed consent form;
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Who have no congenital anomaly;
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Who have no chronic disease;
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Who have undergone no surgical procedure;
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Who have no neurological symptoms;
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Who have no NEC (necrotizing enterocolitis) diagnosis;
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Who are not sedated;
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Who are not hypoglycemic;
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Who have been administered no pharmacological analgesic method 4 hours before;
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Who are born between ≥28 and ≤36+6 gestation weeks, or are in between ≥28 and ≤36+6 gestation weeks during the procedure.
Exclusion Criteria:
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The infants whose parents do not agree to participate in the research and do not sign the informed consent form;
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Who have a congenital anomaly;
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Who have a chronic disease;
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Who had undergone a surgical procedure;
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Who have neurological symptoms;
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Who have NEC (necrotizing enterocolitis) diagnosis;
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Who are sedated;
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Who are hypoglycemic;
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Who have been administered no pharmacological analgesic method 4 hours prior;
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Who were between <28 and >36+6 gestation weeks.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Şişli Kolan International Hastanesi | İstanbul | Şişli | Turkey | 34360 |
Sponsors and Collaborators
- Acibadem University
Investigators
- Principal Investigator: Zehra Kan Öntürk, Assist Prof, Acibadem University
Study Documents (Full-Text)
None provided.More Information
Publications
- ATADEK-2021/15