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Clinical Trials/NCT04033874
NCT04033874
Unknown
N/A

Comparison of the Efficacy of Non-pharmacological Interventions on Pain Levels, Crying Times and Voice Decibels in Newborns: A Randomized Controlled Trial

Eskisehir Osmangazi University1 site in 1 country136 target enrollmentJuly 10, 2019
ConditionsNewborn

Overview

Phase
N/A
Intervention
Not specified
Conditions
Newborn
Sponsor
Eskisehir Osmangazi University
Enrollment
136
Locations
1
Primary Endpoint
Crying times
Last Updated
6 years ago

Overview

Brief Summary

This study aimed to investigate and compare the effects of different non-pharmacological interventions (kangaroo care, holding on mother's lap, white noise listening, ambient sound listening) on newborns' crying times, voice decibels and pain levels during heel-stick procedure

Detailed Description

The study is a prospective, randomized controlled trial including pre and post tests of four groups. The population of the study consisted of newborns who were followed in the Neonatal Service of Eskişehir City Hospital. The number of newborns to be sampled was determined by power analysis. With a 95% confidence interval, 0.25 effect size and 0.85 strength, 34 newborns are planned to be included in each group. Newborns who meet the inclusion criteria will be randomly assigned to the groups. In the randomization process; in the four-group design, the rooms were randomly assigned to the study groups by drawing lots in order to eliminate the probability of influence of newborns from each other. Internal blinding was used as a blinding method in order to ensure complete randomization and to prevent Rosental effect. The randomization was performed by the responsible nurse of the unit who was unaware of the pre-test and post-tests of the application. 1. Four different groups were formed in order to prevent the causes of concern in the randomization of patients who were leveled according to their clinical status in the neonatal intensive care unit. 2. In the absence of neonatal intensive care environment noise, four groups were considered due to the limitation in explaining the benefit, contribution and effect of white noise, kangru care and being in the lap of the mother in reducing pain. 3. The newborns treated with kangaroo care and the mother's lap will be the control groups of each other and the newborns treated with white noise and ambient sound will be the control groups of each other. Research hypotheses: H1. Newborns receiving kangaroo care during the heel-stick procedure have lower pain levels than newborns who are holding on their mother's lap. H2. Newborns receiving kangaroo care during the heel-stick procedure have less crying time than newborns who are holding on their mother's lap. H3. The highest level of sound decibels in the crying process of newborns who receiving kangaroo care during the heel-stick procedure are less than newborns who are holding on their mother's lap. H4. Newborns listened to white noise during the heel-stick procedure have lower pain levels than newborns who listened to ambient sound. H5. Newborns listened to white noise during the heel-stick procedure have less crying time than newborns who listened to ambient sound. H6. The highest level of sound decibels in the crying process of newborns who listened to white noise during the heel-stick procedure are less than newborns listened to ambient sound. In the study, NIPS (Neonatal Infant Pain Scale) will be used to evaluate the pain severity of newborns in addition to the data form prepared by the researchers. During the application, pulse oximetry device will be placed on each newborn right wrist, then heart rate and SpO2 values will be recorded before, during and after the procedure. The device will remain attached to the baby's wrist during the procedure. Then, the pain level will be assessed with NIPS and heel-stick procedure will be initiated. To determine the crying time, the stopwatch shall be turned on and the sound decibel meter shall be turned on to determine the sound decibel. The general pain level of the newborns will be evaluated by one minute before the procedure and their response to the pain for three minutes during and after the procedure.

Registry
clinicaltrials.gov
Start Date
July 10, 2019
End Date
December 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Eskisehir Osmangazi University
Responsible Party
Principal Investigator
Principal Investigator

Pınar Duru

Principal Investigator

Eskisehir Osmangazi University

Eligibility Criteria

Inclusion Criteria

  • Gestation age is between 34-42 weeks
  • Birth weight is between 2500-4000 gr
  • Apgar score of 1 minute and 5 minutes 8 and above
  • Passing the newborn hearing screening test
  • To being followed in the neonatal intensive care unit
  • To being fed at least half an hour before the procedure
  • To being agreed to participate in the study by parents
  • To being never received mechanical ventilation / CPAP support after birth
  • Having none of congenital anomaly

Exclusion Criteria

  • Inability to take blood the first attempt, as the pain level may change
  • Failure of the newborn to pass the hearing screening test
  • Newborns hospitalized from polyclinic and emergency department because heel blood was taken before
  • Refusing to participate in the study by parents

Outcomes

Primary Outcomes

Crying times

Time Frame: Five months

Newborns' crying times during heel-stick procedure will be assessed with the stopwatch

Voice decibels

Time Frame: Five months

Newborns' voice decibels during heel-stick procedure will be assessed with the sound decibel meter

Pain levels

Time Frame: Five months

Newborns' pain levels during heel-stick procedure will be assessed with NIPS (Neonatal Infant Pain Scale)

Study Sites (1)

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