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Management of Healthy Newborn's Body Temperature at Birth

Not Applicable
Not yet recruiting
Conditions
Newborn, Infant
Body Temperature
Delivery Room
Interventions
Other: Interventional group
Other: Standard of care group
Registration Number
NCT06275932
Lead Sponsor
Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
Brief Summary

At birth, the newborn begins a process of adaptation to extrauterine life. One of the phases of this stabilization process is the maintenance of body temperature; indeed, the newborn passes from a warm environment (mother's womb) of around 37°C to an environment with a temperature lower (delivery room) and, therefore, must implement a series of physiological processes to be able to maintain body temperature constant and within ideal ranges through a balance between production and heat loss.

Hypothermia at birth could cause risks or comorbidities such as an increased risk of infant mortality, hypoglycemia, sepsis, metabolic acidosis, respiratory distress syndrome (RDS) and intraventricular hemorrhage (IVH).

One of the factors that affects heat loss in the delivery room is the relationship between surface area, volume and body mass of the newborn. The decrease in body temperature is directly related to gestational age and weight at birth; indeed, this problem is much more present in premature and/or low weight newborns at birth. Even if a full-term newborn has a more developed thermoregulation center than a preterm newborn, this does not mean that this type of newborns is not at risk heat dispersion.

To date, the strategies that are implemented for the physiological newborn are documented in the literature are, in addition to the heat chain described by the World Health Organization (WHO), the implementation of skin-to-skin contact (skin to skin) mother-newborn.

Some studies demonstrating the beneficial effect of this procedure on maintenance of the newborn's body temperature.

The aim of this study is to evaluate two healthcare interventions to prevent heat loss of healthy newborns at birth.

Detailed Description

This study is a prospective, randomized controlled trial design which involves the use of two care interventions (experimental vs standard of care) to prevent heat loss of healthy newborns in the delivery room during contact skin to skin after birth.

Study population includes newborns born by natural birth with a gestational age greater than or equal to 37+0 weeks.

Newborns will be randomly assigned to receive: 1) a thermal blanket (experimental group) , or 2) a bed wetting mat and cotton sheet (standard of care group) that cover them during the skin-to-skin contact after birth.

At birth all newborns will receive the same care required by local procedures.

Research hypothesis:

- the use of a thermal blanket placed on the newborn during the skin-to-skin contact could reduce heat dispersion at the end of the procedure and therefore reduce the percentage of newborns who at the end of skin-to-skin contact have a temperature lower than 36.5°C.

The effectiveness of these interventions will be evaluated by measuring mother and newborn's body temperature at the beginning and the end of skin-to-skin contact.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
776
Inclusion Criteria

For mother

  • Mothers' age over 18 years and good comprehension of Italian language;
  • Signed informed consent of the mother.

For newborn

  • Informed consent signed by both parents, or in the case of a single-parent family, by mother
  • Gestational age at birth greater than or equal to 37+0 weeks
  • Newborns from singleton pregnancies;
  • Both male and female newborns;
  • Newborns who will be born from vaginal birth.
Exclusion Criteria

For mother

  • Mothers who do not want to carry out skin-to-skin contact;
  • Mothers who do not understand/speak the Italian language;
  • Mothers who need assistance procedures that hinder skin-to-skin contact.

For newborn

  • Newborns whose parents decline participation in the study;
  • Newborns with major congenital anomalies (heart, brain, metabolic, gastrointestinal);
  • Newborns born via cesarean section;
  • Newborns whose parents are under 18 years old, in the case of a single parent the mother who is under 18 years;
  • Newborns requiring neonatal resuscitation after birth with obstruction of the skin-to-skin contact.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Interventional groupInterventional groupAll the enrolled newborns will make the skin-to-skin contact with the use of a thermal blanket after birth.
Standard of care groupStandard of care groupAll the enrolled newborns will make the skin-to-skin contact according to local procedure after birth.
Primary Outcome Measures
NameTimeMethod
Newborn's body temperature at the end of skin-to-skin contactAt the beginning and the end skin-to-skin contact, up to three hours after birth.

Newborn's body temperature will be measured at the beginning and the end of skin-to-skin contact with a digital thermometer placed in axillary location. Newborn's body temperature at the end of kin-to-skin contact will be compared between two groups.

Secondary Outcome Measures
NameTimeMethod
Newborns' proportion transferred to the Neonatal Intensive Care Unit (NICU)At discharge from the nursery, measured up to 1 week.

Evaluation of newborns' proportion transferred to the NICU will be collected from electronical medical records.

Newborns' proportion with temperature below 36.0°C at the end of skin-to-skin contact and at arrival in the nurseryAt the end of skin-to-skin contact and at arrival in the nursery, up to six hours after birth.

Evaluation of newborns' proportion with temperature below 36.0°C at the end of skin-to-skin contact and at arrival in the nursery, in variation of the time spent in the delivery room at the end of the skin-to-skin contact, will be calculated in both arms of study measuring newborn's body temperature with a digital thermometer placed in axillary location.

Newborns' proportion with moderate hypothermia (temperature 36.0 - 36.4°C) at the end of skin-to-skin contact and at arrival in the nurseryAt the end of skin-to-skin contact and at arrival in the nursery, up to six hours after birth.

Evaluation of newborns' proportion with moderate hypothermia (temperature 36.0 - 36.4°C) at the end of skin-to-skin contact and at arrival in the nursery, in variation of the time spent in the delivery room at the end of the skin-to-skin contact, will be calculated in both arms of study measuring newborn's body temperature with a digital thermometer placed in axillary location.

Newborns' proportion with hyperthermia (temperature > 37.5°C) at the end of skin-to-skin contact and at arrival in the nurseryAt the end of skin-to-skin contact and at arrival in the nursery, up to six hours after birth.

Evaluation of newborns' proportion with hyperthermia (temperature \> 37.5°C) at the end of skin-to-skin contact and at arrival in the nursery, in variation of the time spent in the delivery room at the end of the skin-to-skin contact, will be calculated in both arms of study measuring newborn's body temperature with a digital thermometer placed in axillary location.

Newborns' average temperature one hour after arriving at the nurseryAt arrival in the nursery, up to six hours after birth.

Evaluation of newborns' average temperature one hour after arriving at the nursery will be calculated in both arms of study measuring newborn's body temperature with a digital thermometer placed in axillary location.

Duration of nursery stayfrom birth until discharge, measured up to 1 week.

Duration of stay in the nursery (hours) will be collected from electronical medical records

Newborns' proportion affected by respiratory distress syndromeAt discharge from the nursery, measured up to 1 week.

Evaluation of newborns' proportion affected by respiratory distress syndrome will be collected from electronical medical records.

Newborns' proportion with a body temperature < 36.5°C when arriving at the nurseryAt the arrival in the nursery, up to six hours after birth.

Evaluation of newborns' proportion with a body temperature \< 36.5°C will be calculated in both arms of study measuring newborn's body temperature with a digital thermometer placed in axillary location when they will arrive at the nursery.

Duration of skin-to-skin contactFrom the beginning until the end of skin-to-skin contact, up to three hours after birth.

Duration of skin-to-skin contact (minutes) will be collected from electronical medical records

Newborns' proportion exclusively breastfed at dischargeAt discharge from the nursery, measured up to 1 week.

Evaluation of Newborns' proportion exclusively breastfed at discharge will be collected from electronical medical records

Type of breastfeeding at dischargeAt discharge from the nursery, measured up to 1 week.

Evaluation of the type of breastfeeding at discharge will be collected from electronical medical records.

Newborns' proportion with hypoglycemia during hospitalizationAt discharge from the nursery, measured up to 1 week.

Evaluation of newborns' proportion with hypoglycemia during hospitalization will be collected from electronical medical records

Newborns' weight loss at dischargeAt discharge from the nursery, measured up to 1 week.

Percentage of Newborns' weight loss at discharge will be collected from electronical medical records.

Mortality before discharge from hospitalAt discharge from the nursery, measured up to 1 week.

Evaluation of mortality before discharge from hospital will be collected from electronical medical records.

Trial Locations

Locations (1)

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico

🇮🇹

Milan, Italy

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