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The Effect of Skin-to-skin Contact at Birth

14 de junho de 2026 atualizado por: Tugce Sonmez, Gaziantep Islam Science and Technology University

The Effect of Skin-to-skin Contact at Birth on Birth Outcomes and Parenting Behavior

To determine the effects of skin-to-skin contact at birth on birth outcomes (placental delivery time, postpartum pain level, time of first breastfeeding, and breastfeeding motivation) and on postpartum parenting behavior.

Visão geral do estudo

Descrição detalhada

Skin-to-skin contact (STSC) involves placing the baby on the mother's chest for at least one hour during or immediately after birth. After birth, healthy, full-term babies who receive STSC will orient themselves toward their mother's breast and nipple and begin suckling within approximately one hour. This practice has many benefits for both mother and baby. Looking at the benefits for the mother, these include earlier placental separation, reduced postpartum bleeding, increased breastfeeding self-efficacy, and decreased stress levels in the mother. Furthermore, the rise in oxytocin levels in the mother within the first hour after birth promotes the development and strengthening of the bond between mother and baby. The benefits for the baby include a reduction in adverse outcomes associated with birth stress, effective thermoregulation, less and shorter crying, a decrease in the likelihood of apnea, less physiological weight loss, and less stress response to painful procedures. At the same time, it has been shown that SC reduces the rate of formula supplementation in hospitals, increases the initiation of breastfeeding and the level of exclusive breastfeeding, and leads to successful first breastfeeding and optimal suckling. The timing and duration of skin-to-skin contact (STSC) vary. In this study, skin-to-skin contact will be performed immediately after birth.

STSC at birth or immediately after birth: The newborn is placed face-to-face on the mother's abdomen or chest within the first minute after birth. If medically necessary, aspiration can be performed while the baby is on the mother's abdomen or chest, and the baby is thoroughly dried. To prevent heat loss, the baby's back is covered with a pre-warmed blanket and a hat is placed on the head. All other interventions on the newborn can be delayed until at least the end of the first hour after birth or the first successful breastfeeding.

Skin-to-skin contact between the mother and baby is noted as one of the most effective practices to support placental separation during the third stage of labor. This practice not only contributes to the baby's physiological adaptation but also strengthens the mother-baby bond. Skin-to-skin contact is reported to increase oxytocin release, helping the placenta separate more easily and quickly.

The first two hours after birth, when newborns are most sensitive to sensory cues such as their mother's warmth, touch, and smell, are considered the most appropriate time for initiating breastfeeding and establishing bonding. The aim of skin-to-skin contact is to initiate the first breastfeeding after birth as early as possible. This helps to initiate breastfeeding early, strengthening the emotional bond between mother and baby and contributing to a longer breastfeeding period. It is recommended that breastfeeding begin within the first half hour after birth through skin-to-skin contact.

Childbirth is a unique process that is perceived and experienced differently by each woman and is considered an important step in the transition to parenthood. Ensuring that this process occurs in line with the mother's expectations helps to make the postpartum period more peaceful and healthy. The baby, who is in constant physical contact with the mother during the intrauterine period, maintains continuity of communication by establishing contact with the mother after birth. Maintaining this contact in the postpartum period is an important requirement that supports the physical and psychological well-being of both the mother and the baby.

Skin-to-skin contact (STSC), as the first physical bond established between the mother and newborn immediately after birth, is a fundamental practice that brings many positive physiological and psychosocial effects. In this context, examining the effects of skin-to-skin contact during birth on both birth outcomes (such as placental separation time, postpartum pain, timing of first breastfeeding, and motivation) and parenting behaviors is of great importance for developing evidence-based approaches in birth care.

The findings obtained will contribute to midwifery practices in childbirth and postnatal care, thereby providing a basis for strengthening policies aimed at supporting maternal and newborn health.

Tipo de estudo

Intervencional

Inscrição (Estimado)

96

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Locais de estudo

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Sim

Descrição

Inclusion Criteria:

  • Vaginal delivery
  • Primiparous pregnancy
  • Delivery at 37 weeks or later
  • Single, live fetus
  • Not a high-risk pregnancy
  • Not an individual with special needs
  • Able to communicate

Exclusion Criteria:

  • Women who Have a multiple pregnancy,
  • Develop complications requiring emergency intervention in the mother or baby after delivery,
  • Have their baby admitted to the neonatal intensive care unit after delivery,
  • Have a cesarean section,
  • Withdraw from the study will be excluded from the research.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Cuidados de suporte
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Solteiro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Sem intervenção: Control group
Mothers and newborns in the control group will not receive any procedures; they will undergo the hospital's routine procedures.
Experimental: Immediate Skin-to-Skin Contact After Birth (intervention group)
Immediate skin-to-skin contact after birth: If the newborn requires no intervention, they will be immediately placed on the mother's chest (before cord clamping) and skin-to-skin contact will begin. Skin-to-skin contact will be maintained for approximately 60 minutes until the first breastfeeding occurs. All routine procedures performed in the delivery room for the newborn (except for weight measurement) will be performed while the newborn is on the mother's chest.
Immediate skin-to-skin contact after birth: If the newborn requires no intervention, they will be immediately placed on the mother's chest (before cord clamping) and skin-to-skin contact will begin. Skin-to-skin contact will be maintained for approximately 60 minutes until the first breastfeeding occurs. All routine procedures performed in the delivery room for the newborn (except for weight measurement) will be performed while the newborn is on the mother's chest.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Personal Information Form
Prazo: baseline
The form prepared by the researchers consists of 14 questions about the mothers' socio-demographic characteristics, obstetric characteristics, and newborns.
baseline
Breastfeeding Motivation Scale
Prazo: Periprocedural
The Breastfeeding Motivation Scale, based on Self-Determination Theory, was developed by Peleg et al. (2015). It was adapted into Turkish by Şahin et al. in 2017, and a validity and reliability study was conducted. Exploratory factor analysis revealed that the Turkish version consists of 23 items and five sub-factors for primiparous mothers, and 24 items and six sub-factors for multiparous mothers. According to the calculated Cronbach's alpha value, the Breastfeeding Motivation Scale is a highly reliable scale for both primiparous (Cronbach's alpha: 0.887) and multiparous (Cronbach's alpha: 0.914) mothers. The scale consists of 24 items and 5 sub-dimensions. The items are rated on a 4-point Likert scale, with each item receiving a score between 1 and 4. The total score of the scale is calculated by averaging the scores of the sub-dimensions. As the score obtained from a subscale increases, it is interpreted as an increase in the motivation represented by that subscale.
Periprocedural
VAS
Prazo: Periprocedural
The VAS (Visual Assessment Scale) is one of the most commonly used measurement tools for determining pain intensity. The VAS consists of a line drawn on a horizontal or vertical axis, 10 cm or 100 mm long. At one end of this line is the word "no pain," and at the other end is the word "unbearable pain." The distance from the lowest VAS value to the point marked by the pregnant woman is measured in cm or mm to determine the numerical value of the pain intensity. The evaluation is based on these markings. The VAS is considered a successful measurement tool for evaluating the effectiveness of pain relief methods (Demir, 2012; Carvalho & Cohen, 2013).
Periprocedural
Postnatal Parenting Behavior Scale
Prazo: Periprocedural

The scale was developed by Britton et al. in 2001 to evaluate the behaviors exhibited by parents during their first interactions after birth (Britton et al., 2001). The Turkish adaptation, validity, and reliability study of the scale was conducted by Çalışır et al. (2009) (Çalışır et al., 2009).

This scale aims to evaluate the parenting behaviors of the mother or father during their first encounter with their baby immediately after birth through observation. In the six-item scale, the observer records whether the parent exhibits each behavior; behaviors performed are indicated with a "+" sign, and those not performed with a "-" sign. A score of "1" is given for each observed behavior, and a score of "0" for each unobserved behavior. Thus, the total score that can be obtained from the scale ranges from 0 to 6.

A high score indicates that the parent exhibits more positive and supportive parenting behaviors towards their baby.

Periprocedural
Skin-to-Skin Contact, Placental Separation, and Breastfeeding Process Tracking Form
Prazo: Periprocedural
This form was created by researchers. It is used to record information about when mothers started skin-to-skin contact, the duration of skin-to-skin contact, the time they started breastfeeding, the duration of breastfeeding, and the time it took for placental separation.
Periprocedural

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

  • Cadeira de estudo: Serap Ejder Apay, Prof., Ataturk University
  • Cadeira de estudo: Mehtap Begüm Orak, Master's student, Ataturk University

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

1 de julho de 2026

Conclusão Primária (Estimado)

1 de dezembro de 2026

Conclusão do estudo (Estimado)

1 de junho de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

5 de março de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

14 de junho de 2026

Primeira postagem (Real)

18 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

18 de junho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

14 de junho de 2026

Última verificação

1 de março de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

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INDECISO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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