Non-pharmacological Methods in Pain Managment During Heel Stick in Preterm Infants ((pain))
15 марта 2022 г. обновлено: Negarin Akbari
The Effect of Facilitated Tucking, Maternal Breast Milk Odor and Non Nutritive Sucking During Heel Stick on Procedural Pain in Premature Neonates
Aims and objectives: This study was performed to examine the effects of Non-nutritive sucking, breast milk odor, and Facilitated tucking on preterm infant pain before, during, and after heel-stick procedures.
Design: A randomized clinical trial in a single center.
Methods:
The study was conducted on 144 premature infants with a gestational age of 31 to 36 weeks and 6 days hospitalized in the neonatal intensive care unit of Shahid Sayad Shirazi Hospital in Iran. Neonates were randomly assigned to four groups: 36 babies were included in the Non-nutritive sucking(1st Group), 36 in breast milk odor (2nd Group), 36 in Facilitated tucking (3rd Group), and 36 in the control group (4th Group). Pain score, heart rate, oxygen saturation, and respiratory rate of the babies in all groups before, during, and after the procedure were evaluated by two nurses independently.
Обзор исследования
Статус
Завершенный
Подробное описание
Aim: Due to the necessity of various painful procedures and their side effects on infants, pharmacological and non-pharmacological methods are adopted to reduce the pain. Since pharmacological methods can be associated with several side effects, it is better to use non-pharmacological methods for pain control in newborns. Therefore, the purposes of this study were to compare the effects of three different methods (including Non-nutritive sucking, breast milk odor, and Facilitated tucking) on preterm infant pain before, during, and after heel-stick procedures.
Method: The study was conducted on 144 premature infants with a gestational age of 31 to 36 weeks and 6 days hospitalized in the neonatal intensive care unit of Shahid Sayad Shirazi Hospital, Iran. Initially, neonates are divided into two groups according to gestational age (including neonates between 31-33 weeks and 34-36 weeks) to moderate the confounding effect of the age, and then the allocation of neonates to four groups was performed.
Using the stratification block randomization method, 36 babies were included in the Non-nutritive sucking(1st Group), 36 in breast milk odor (2nd Group), 36 in Facilitated tucking (3rd Group), and 36 in the control group (4th Group). Two researchers viewed the recorded videos independently and evaluate the heart rate, oxygen saturation, respiratory rate, and neonatal pain at 1st,2nd,3rd minute before the procedure, during, and at 1st,2nd,3rd minutes after the procedure according to the Premature Infant Pain Profile (PIPP).
Тип исследования
Интервенционный
Регистрация (Действительный)
144
Фаза
- Непригодный
Контакты и местонахождение
В этом разделе приведены контактные данные лиц, проводящих исследование, и информация о том, где проводится это исследование.
Места учебы
-
-
Golestan
-
Gorgān, Golestan, Иран, Исламская Республика, 017
- Golestan University of Medical sciences
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Критерии участия
Исследователи ищут людей, которые соответствуют определенному описанию, называемому критериям приемлемости. Некоторыми примерами этих критериев являются общее состояние здоровья человека или предшествующее лечение.
Критерии приемлемости
Возраст, подходящий для обучения
От 1 день до 1 неделя (Ребенок)
Принимает здоровых добровольцев
Да
Полы, имеющие право на обучение
Все
Описание
Inclusion Criteria:
- Week of gestation is between 31 and 36 weeks
- Not being exposed to a painful procedure at least 1 hour before the interventions
- At least 1 hour has passed since feeding
- Not taking analgesics and/or sedatives in the last 4 hours
- Body weight of 1000 grams or more
- Having mother's milk
- Not exceeding the 10th day of postnatal age
Exclusion Criteria:
- Having ventilator support
- Having a congenital anomaly
- Using analgesic / narcotic analgesic drugs
- Continuous sedative treatment
- Having a congenital malformation that may cause asphyxia and affect respiration
- Having intracranial bleeding
Учебный план
В этом разделе представлена подробная информация о плане исследования, в том числе о том, как планируется исследование и что оно измеряет.
Как устроено исследование?
Детали дизайна
- Основная цель: Профилактика
- Распределение: Рандомизированный
- Интервенционная модель: Параллельное назначение
- Маскировка: Одинокий
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
|---|---|
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Экспериментальный: Breast milk odor group
It is a non-pharmacological method of pain control in which 3 cc of breast milk will be dripped onto a sterile pad and It will be placed at a distance of 10 cm from the nose of the newborn.
Precisely, premature newborns' own mothers' milk will be used.
For this, mothers of newborns will be contacted and breast milk will be provided for the day of the procedure.
|
The researcher applied the breast milk that dripped on the pad for 3 minutes before the heel stick for 36 premature newborns in the breast milk odor group.
About three cc breast milk dripped onto a sterile pad and placed at a distance of 10 cm from the nose of the newborn.
It continued until 3 minutes after the invasive procedure.
Heart rate, arterial oxygen saturation, and respiration rate were recorded in this group before the study.
Then, to evaluate the pain in the infants, a video camera was placed on the incubator.
The infants in each group were filmed from three minutes before the procedure to three minutes after.
Neonatal pain was measured at 1, 2, and 3 minutes before, during, and at 1, 2, and 3 minutes after the procedure by two researchers independently using the new version Premature Infant Pain Profile (PIPP).
Другие имена:
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Экспериментальный: Facilitated tucking group
It is a non-pharmacological method of pain control in which the arms and legs are slowly contracted and placed close to the body.
In this method, the baby is placed on its side, the baby's back is gently bent, the legs are folded at an angle of more than 90 degrees, the shoulders are folded up to 90 degrees, and the care hands are placed either on the head near the mouth or Placed on the baby's face.
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The Facilitated tucking position was given to 36 premature newborns in the Facilitated tucking group, from 3 minutes before to 3 minutes after the heel stick procedure.
Premature newborns were kept in the facilitated tucking position by the investigator using the incubator windows without opening the incubator cover to prevent heat loss of the newborn.
Heart rate, arterial oxygen saturation, and respiration rate were recorded in this group before the study.
Then, to evaluate the pain in the infants, a video camera was placed on the incubator.
The infants in each group were filmed from three minutes before the procedure to three minutes after.
Neonatal pain was measured at 1, 2, and 3 minutes before, during, and at 1, 2, and 3 minutes after the procedure by two researchers independently using the new version Premature Infant Pain Profile (PIPP).
|
|
Экспериментальный: Non-nutritive sucking group
It is a non-pharmacological method used to control pain in infants.
In this method, babies suck without receiving the nutrient.
This can be done by a pacifier, a parent's hand or a nurse.
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36 premature newborns who were in the non-nutritive sucking group were given a silicone pacifier suitable for the week of the baby's mouth from 3 minutes before to 3 minutes after the heel stick.
Heart rate, arterial oxygen saturation, and respiration rate were recorded in this group before the study.
Then, to evaluate the pain in the infants, a video camera was placed on the incubator.
The infants in each group were filmed from three minutes before the procedure to three minutes after.
Neonatal pain was measured at 1, 2, and 3 minutes before, during, and at 1, 2, and 3 minutes after the procedure by two researchers independently using the new version Premature Infant Pain Profile (PIPP).
Другие имена:
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Экспериментальный: control grup
The control group will consist of 36 premature newborns who are routinely applied in the clinic.
In the clinic where the research was conducted, no attempt is made to reduce pain during heel stick.
|
The control group will consist of 36 premature newborns who are routinely applied in the clinic. In the clinic where the research was conducted, no attempt is made to reduce pain during heel stick. Heart rate, arterial oxygen saturation, and respiration rate were recorded in this group before the study. Then, to evaluate the pain in the infants, a video camera was placed on the incubator. The infants in each group were filmed from three minutes before the procedure to three minutes after. Neonatal pain was measured at 1, 2, and 3 minutes before, during, and at 1, 2, and 3 minutes after the procedure by two researchers independently using the new version Premature Infant Pain Profile (PIPP). |
Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Pain score of preterm infants assessed on the Premature Infant Pain Profile Revised (PIPP-R)
Временное ограничение: Pain was measured at 1 minutes before the procedure by two researchers independently.
|
PIPP is a valid instrument that can be used to assess infants' response to pain.
The instrument estimates the baby's pain based on assigning a score of zero to four to each of the fetal ages, behavioral status, maximum heart rate, minimum oxygen saturation, eyebrow bulges, eye presses, lip and nose creases.
This tool's minimum and maximum pain scores are zero and 21, respectively.
|
Pain was measured at 1 minutes before the procedure by two researchers independently.
|
|
Pain score of preterm infants assessed on the Premature Infant Pain Profile Revised (PIPP-R)
Временное ограничение: Pain was measured at 2 minutes before the procedure by two researchers independently.
|
PIPP is a valid instrument that can be used to assess infants' response to pain.
The instrument estimates the baby's pain based on assigning a score of zero to four to each of the fetal ages, behavioral status, maximum heart rate, minimum oxygen saturation, eyebrow bulges, eye presses, lip and nose creases.
This tool's minimum and maximum pain scores are zero and 21, respectively.
|
Pain was measured at 2 minutes before the procedure by two researchers independently.
|
|
Pain score of preterm infants assessed on the Premature Infant Pain Profile Revised (PIPP-R)
Временное ограничение: Pain was measured at 3 minutes before the procedure by two researchers independently.
|
PIPP is a valid instrument that can be used to assess infants' response to pain.
The instrument estimates the baby's pain based on assigning a score of zero to four to each of the fetal ages, behavioral status, maximum heart rate, minimum oxygen saturation, eyebrow bulges, eye presses, lip and nose creases.
This tool's minimum and maximum pain scores are zero and 21, respectively.
|
Pain was measured at 3 minutes before the procedure by two researchers independently.
|
|
Pain score of preterm infants assessed on the Premature Infant Pain Profile Revised (PIPP-R)
Временное ограничение: Pain was measured during the procedure by two researchers independently.
|
PIPP is a valid instrument that can be used to assess infants' response to pain.
The instrument estimates the baby's pain based on assigning a score of zero to four to each of the fetal ages, behavioral status, maximum heart rate, minimum oxygen saturation, eyebrow bulges, eye presses, lip and nose creases.
This tool's minimum and maximum pain scores are zero and 21, respectively.
|
Pain was measured during the procedure by two researchers independently.
|
|
Pain score of preterm infants assessed on the Premature Infant Pain Profile Revised (PIPP-R)
Временное ограничение: Pain was measured at 1 minutes after the procedure by two researchers independently.
|
PIPP is a valid instrument that can be used to assess infants' response to pain.
The instrument estimates the baby's pain based on assigning a score of zero to four to each of the fetal ages, behavioral status, maximum heart rate, minimum oxygen saturation, eyebrow bulges, eye presses, lip and nose creases.
This tool's minimum and maximum pain scores are zero and 21, respectively.
|
Pain was measured at 1 minutes after the procedure by two researchers independently.
|
|
Pain score of preterm infants assessed on the Premature Infant Pain Profile Revised (PIPP-R)
Временное ограничение: Pain was measured at 2 minutes after the procedure by two researchers independently.
|
PIPP is a valid instrument that can be used to assess infants' response to pain.
The instrument estimates the baby's pain based on assigning a score of zero to four to each of the fetal ages, behavioral status, maximum heart rate, minimum oxygen saturation, eyebrow bulges, eye presses, lip and nose creases.
This tool's minimum and maximum pain scores are zero and 21, respectively.
|
Pain was measured at 2 minutes after the procedure by two researchers independently.
|
|
Pain score of preterm infants assessed on the Premature Infant Pain Profile Revised (PIPP-R)
Временное ограничение: Pain was measured at 3 minutes after the procedure by two researchers independently.
|
PIPP is a valid instrument that can be used to assess infants' response to pain.
The instrument estimates the baby's pain based on assigning a score of zero to four to each of the fetal ages, behavioral status, maximum heart rate, minimum oxygen saturation, eyebrow bulges, eye presses, lip and nose creases.
This tool's minimum and maximum pain scores are zero and 21, respectively.
|
Pain was measured at 3 minutes after the procedure by two researchers independently.
|
Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Heart rate during heel stick
Временное ограничение: from 4 minutes before heel stick to 4 minute after heel stick
|
Heart rate initially was recorded in each group 4 minutes before starting any intervention.
Then, 1,2, and 3 minutes before heel stick, During heel stick, and 1,2,3 minutes after heel stick it again measured (totally eight times).
|
from 4 minutes before heel stick to 4 minute after heel stick
|
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Respiratory rate
Временное ограничение: From 4 minutes before heel stick to 4 minute after heel stick
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Respiratory rate initially was recorded in each group 4 minutes before starting any intervention.
Then, 1,2, and 3 minutes before heel stick, During heel stick, and 1,2,3 minutes after heel stick it again measured (totally eight times).
|
From 4 minutes before heel stick to 4 minute after heel stick
|
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Oxygen saturation
Временное ограничение: From 4 minutes before heel stick to 4 minute after heel stick
|
Oxygen saturation initially was recorded in each group 4 minutes before starting any intervention.
Then, 1,2, and 3 minutes before heel stick, During heel stick, and 1,2,3 minutes after heel stick it again measured (totally eight times).
|
From 4 minutes before heel stick to 4 minute after heel stick
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Другие показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Crying time
Временное ограничение: During procedure (During heel stick the total crying time was measured from where it starts until the over.)
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The researcher recorded the crying time in second (sec) during heel stick.
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During procedure (During heel stick the total crying time was measured from where it starts until the over.)
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Соавторы и исследователи
Здесь вы найдете людей и организации, участвующие в этом исследовании.
Спонсор
Следователи
- Главный следователь: Negarin Akbari, PhD student, Istanbul un'vers'ty cerrahpasa-Istanbul,Turkey
Даты записи исследования
Эти даты отслеживают ход отправки отчетов об исследованиях и сводных результатов на сайт ClinicalTrials.gov. Записи исследований и сообщаемые результаты проверяются Национальной медицинской библиотекой (NLM), чтобы убедиться, что они соответствуют определенным стандартам контроля качества, прежде чем публиковать их на общедоступном веб-сайте.
Изучение основных дат
Начало исследования (Действительный)
15 декабря 2021 г.
Первичное завершение (Действительный)
25 декабря 2021 г.
Завершение исследования (Действительный)
2 января 2022 г.
Даты регистрации исследования
Первый отправленный
18 января 2022 г.
Впервые представлено, что соответствует критериям контроля качества
15 марта 2022 г.
Первый опубликованный (Действительный)
16 марта 2022 г.
Обновления учебных записей
Последнее опубликованное обновление (Действительный)
16 марта 2022 г.
Последнее отправленное обновление, отвечающее критериям контроля качества
15 марта 2022 г.
Последняя проверка
1 марта 2022 г.
Дополнительная информация
Термины, связанные с этим исследованием
Дополнительные соответствующие термины MeSH
Другие идентификационные номера исследования
- 1400829255739
Планирование данных отдельных участников (IPD)
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НЕТ
Информация о лекарствах и устройствах, исследовательские документы
Изучает лекарственный продукт, регулируемый FDA США.
Нет
Изучает продукт устройства, регулируемый Управлением по санитарному надзору за качеством пищевых продуктов и медикаментов США.
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Эта информация была получена непосредственно с веб-сайта clinicaltrials.gov без каких-либо изменений. Если у вас есть запросы на изменение, удаление или обновление сведений об исследовании, обращайтесь по адресу register@clinicaltrials.gov. Как только изменение будет реализовано на clinicaltrials.gov, оно будет автоматически обновлено и на нашем веб-сайте. .