The NEU-STIM Trial
Ориентир для пациента и семьи
Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: Repeated tactile stimulation, Selective tactile stimulation.
- Кому может быть актуально
- Состояния в реестре: Infant, Premature, Diseases, Birth, Preterm. Базовые параметры: до 32 Weeks · Все.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- Австрия, Бельгия, Хорватия, Чехия, Дания +14
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Официальное название
A Randomised Trial of Repetitive Versus Selective Tactile Stimulation for Preterm Infants at Birth: The NEU-STIM Trial
Обзор
The aim of this study is to determine the effect of repetitive tactile stimulation compared to selective stimulation on oxygenation of the infant at 5 minutes after birth. Infants born before 32 weeks of gestation will be included in this trial. This is a stepped-wedge cluster randomised controlled trial. The participating centre, rather than the individual infant, will be the unit of randomisation. This design is appropriate to test the effect of an intervention that encompasses a behavioral aspect - in this case the performance of tactile stimulation.
Подробное описание
Rationale: A randomised study demonstrated that preterm infants who received repetitive stimulation at birth (10 second episodes of stroking of the soles of the feet and/or back, followed by 10 seconds rest) showed an increase in respiratory effort. This may in turn improve clinical outcomes as improved breathing effort may reduce the need for invasive respiratory support. Tactile stimulation can be immediately and easily performed at birth at no extra cost. It therefore has great potential to be implemented in delivery rooms (DRs) worldwide.
Objective: To determine the effect of repetitive tactile stimulation compared to selective stimulation on oxygenation of the infant at 5 minutes after birth.
Study design: This is a stepped-wedge cluster randomised controlled trial. The participating centre, rather than the individual infant, will be the unit of randomisation. This design is appropriate to test the effect of an intervention that encompasses a behavioral aspect - in this case the performance of tactile stimulation.
Study population: Infants born before 32 weeks of gestation will be included in this trial.
Intervention: At the start of the study, each participating centre will perform selective tactile stimulation in accordance with international guidelines, as is their usual practice. Clinicians will gently rub the back, chest, extremities or soles of the feet if they consider the breathing of the infant to be insufficient or absent. In the second stage of the study, centres will be randomised to switch their stimulation approach to repetitive stimulation. Clinicians will then gently rub the back, chest, extremities or soles of the feet for 10 seconds. To avoid extinction of the stimulatory effect (reflex), every 10 second period of stimulation will be followed by 10 seconds of rest (no stimulation). Repetitive stimulation will be performed for the first 5 minutes of life, or longer if the breathing is still considered insufficient or absent.
Main study parameter: The proportion of infants with pre-ductal oxygen saturation (SpO2) ≥ 80%.
Вмешательства
- Процедура Repeated tactile stimulation
See arm - Процедура Selective tactile stimulation
See arm
Первичные конечные точки
- SpO2>80 [Срок оценки: At 5 minutes of life]
Вторичные конечные точки (12)
- Heart rate [Срок оценки: At 5 minutes after birth]
- Number of infants who received CPAP <10min [Срок оценки: Within 10 minutes after birth]
- Number of infants who received PPV <10min [Срок оценки: Within 10 minutes after birth]
- Number of infants who were intubated <10min [Срок оценки: Within 10 minutes after birth]
- Number of infants who received chest compressions <10min [Срок оценки: Within 10 minutes after birth]
- Number of infants who were administered adrenaline <10min [Срок оценки: Within 10 minutes after birth]
- Number of infants who were administered volume expansion <10min [Срок оценки: Within 10 minutes after birth]
- Max FiO2 [Срок оценки: In the first 10 minutes after birth]
- Death <10min [Срок оценки: Within 10 minutes after birth]
- Number of infants who were supported by CPAP in first week [Срок оценки: In the first week after birth]
- Number of infants who received surfactant in first week [Срок оценки: In the first week after birth]
- Surfactant doses [Срок оценки: In the first week after birth]
Критерии участия
Критерии включения
- Infants born before 32 weeks of gestation can be included in this trial after parental consent.
Критерии исключения
- Infants will be excluded if they are found to have a congenital abnormality or condition that has an adverse effect on breathing/ventilation or oxygenation, including: congenital diaphragmatic hernia, trachea-oesophageal fistula, cyanotic heart disease and surfactant protein deficiency. Many of the infants enrolled in the study will later be diagnosed with respiratory distress syndrome (RDS); this will not render them ineligible for inclusion.
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Параллельные группы
- Маскирование
- Простое слепое
- Основная цель
- Лечение
Центры проведения
Норвегия · 6 центров
- Haukeland University Hospital — Bergen
- Oslo University Hospital, Ulleval — Oslo
- Oslo University Hospital — Oslo
- Stavanger University Hospital — Stavanger
- University Hospital of North Norway — Tromsø
- St Olav's Hospital Trondheim — Trondheim
Польша · 6 центров
- Jan Biziel University Hospital No. 2 in Bydgoszcz — Bydgoszcz
- Medical University of Gdansk — Gdansk
- Medical University of Silesa — Katowice
- University of Medical Sciences — Poznan
- Provincial Hospital — Rzeszów
- Wrocław Medical University — Wroclaw
Венгрия · 4 центра
- First dept of Obstetrics and Gynaecology, Semmelweis University — Budapest
- Second Semmelweis University — Budapest
- University of Debrecen — Debrecen
- Bács-Kiskun County Teaching Hospital — Szeged
Германия · 3 центра
- University Hospital Carl Gustav Carus — Dresden
- University Hospital Dusseldorf — Düsseldorf
- University Hospital Tubingen — Tübingen
Ирландия · 3 центра
- National Maternity Hospital — Dublin
- Coombe Women & Infants University Hospital — Dublin
- University Hospital Galway — Galway
Румыния · 3 центра
- University Ovidius of Constanta — Constanța
- Clinical County Emergency Hospital Sibiu — Sibiu
- George Emil Palade University of Medicine — Târgu Mureş
Хорватия · 2 центра
- Clinical Hospital Center Rijeka — Rijeka
- Clinical Center Split — Split
Чехия · 2 центра
- General Faculty Hospital in Prague — Prague
- Institute for Mother and Child Care — Prague
Дания · 2 центра
- Aarhus University Hospital — Aarhus
- Rigshospitalet Copenhagen — Copenhagen
Нидерланды · 2 центра
- Leiden University Medical Center — Leiden
- Erasmus MC Sophia Kinderziekenhuis — Rotterdam
Украина · 2 центра
- Bukovyna State Medical University, Chernivtsi — Chernivtsi
- Sumy State University — Sumy
Австрия · 1 центр
- Medical University of Graz — Graz
Бельгия · 1 центр
- Liège University Hospital — Liège
Греция · 1 центр
- Aristotle University of Thessaloniki — Thessaloniki
Iceland · 1 центр
- Landspitali University Hospital — Reykjavik
Италия · 1 центр
- Ospedale dei Bambini Vittore Buzzi — Milan
Португалия · 1 центр
- Hospital de Braga — Braga
Испания · 1 центр
- La Fe University Hospital — Valencia
Turkey (Türkiye) · 1 центр
- University of Health Sciences Sancaktepe Ilhan Varank Training and Research Hospital, Ista — Istanbul
Публикации
- Dekker J, Hooper SB, Martherus T, Cramer SJE, van Geloven N, Te Pas AB. Repetitive versus standard tactile stimulation of preterm infants at birth - A randomized controlled trial. Resuscitation. 2018 Jun;127:37-43. doi: 10.1016/j.resuscitation.2018.03.030. Epub 2018 Mar 23. PMID 29580959
- Dekker J, O'Donnell CPF, Rudiger M, Te Pas AB, Pauws SC. Repeated versus selective tactile stimulation for preterm infants at birth: protocol and statistical analysis plan for a stepped-wedge cluster randomised controlled trial (NEU-stim trial). BMJ Open. 2026 Jun 2;16(6):e114181. doi: 10.1136/bmjopen-2025-114181. PMID 42229963
Идентификаторы
NCT: NCT05942924 · N22.121