Tandem: Skin-to-skin Transfer From the Delivery Room to the Neonatal Unit (Tandem)

January 9, 2024 updated by: Erasme University Hospital

Tandem: Skin-to-skin Transfer From the Delivery Room to the Neonatal Unit for Neonates Above 1500 g

Immediate skin-to-skin contact (SSC) is already standard care for healthy term newborns, but its use for term or preterm newborns requiring admission to neonatal unit (NICU) with or without respiratory support is challenging. This study aimed to assess the safety and feasibility of SSC during the transfer of newborn infants, using a new purpose-built mobile shuttle care-station, called "Tandem".

A monocentric prospective observational study was conducted at the tertiary referral center of the Université libre de Bruxelles in Brussels, Belgium Infants born with a birth weight above 1500g were eligible. Following initial stabilization, infants were placed in SSC with one of their parents and transferred to the NICU using the Tandem.

Study Overview

Detailed Description

Prior to delivery, the trained neonatal team prepares both the Tandem and a transport incubator as a backup. Delayed umbilical cord clamping will be performed for at least one minute unless prompt resuscitation required. Then, infants will be stabilized on a resuscitation table following European Resuscitation Council guidelines, with applying electrodes for continous monitoring of heart rate, saturation and temperature. After initial stabilization respiratory support will be continued if needed using the Tandem's gas supply. In cases when, antibiotics or continuous IV glucose infusion are necessary, peripheral venous catheters will be placed before departure. In case of respiratory support, nasogastric tube will be insterted. Infants will be then transferred to the NICU under the supervision of a pediatric nurse and/or pediatrician with the Tandem in skin-to-skin position with either the mother or the father. Whenever possible, SSC will be continued for at least 120 minutes before placing the infant in an incubator. Blood glucose measurement will take place at least once during the procedure.

Study Type

Observational

Enrollment (Actual)

73

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Anderlecht
      • Brussels, Anderlecht, Belgium, 1070
        • Neonatal Unit Hopital Erasme

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Neonates over 31 weeks of gestational age and over 1500 grams requiring admission to the neonatal unit

Description

Inclusion Criterias:

  • neonates with an estimated foetal weight above1500 grams
  • neonates requiring admission to the neonatal intensive care unit
  • neonates requiring or not non-invasive respiratory support
  • neonates with at least one parent who has a good understanding of the method of transfer

Exclusion Criteria:

  • neonates presenting a malformation incompatible with this type of transfer
  • neonates with invasive ventilation

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Feasibility of Skin-to-skin transfer
Time Frame: 0-2 hours of life
Rate of discontinuation of the skin-to-skin was measured
0-2 hours of life

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Safety of Skin-to-skin transfer - Hemodynamic
Time Frame: 0-2 hours of life
Heart rate measured in bpm (considered normal range: 120-180 bpm )
0-2 hours of life
Safety of Skin-to-skin transfer - Oxygenisation
Time Frame: 0-2 hours of life
Saturation measured in % ( considered normal >92 %)
0-2 hours of life
Safety of Skin-to-skin transfer- Temperature
Time Frame: 0-2 hours of life
Temperature measured in Celsius ( considered normal range: 36.5-37.5 C)
0-2 hours of life
Safety of Skin-to-skin transfer - Blood glucose
Time Frame: 0-2 hours of life
Blood glucose level measured in mg/dL at least once during the first two hours of life (considered normal range: 30-100 mg/dL)
0-2 hours of life
Parental and nursing satisfaction
Time Frame: 0-1 days of life
Parental and nursing satisfaction with skin-to-skin transfer via the Tandem from the delivery suite or the operating theater to the NICU were rated on a scale from 1 to 10 (10 being the most satisfied)
0-1 days of life
Breastfeeding at hospital discharge
Time Frame: 1 day (at discharge)
Exclusive breastfeeding rate at discharge
1 day (at discharge)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Dorottya KELEN, Erasme University Hospital

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 3, 2017

Primary Completion (Actual)

December 30, 2019

Study Completion (Actual)

April 30, 2020

Study Registration Dates

First Submitted

November 30, 2023

First Submitted That Met QC Criteria

January 9, 2024

First Posted (Actual)

January 10, 2024

Study Record Updates

Last Update Posted (Actual)

January 10, 2024

Last Update Submitted That Met QC Criteria

January 9, 2024

Last Verified

November 1, 2023

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Preterm Birth

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