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The Effect of Skin-to-skin Contact at Birth

14 giugno 2026 aggiornato da: 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.

Panoramica dello studio

Descrizione dettagliata

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 di studio

Interventistico

Iscrizione (Stimato)

96

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

Descrizione

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.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Terapia di supporto
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Separare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Nessun intervento: Control group
Mothers and newborns in the control group will not receive any procedures; they will undergo the hospital's routine procedures.
Sperimentale: 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Personal Information Form
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Cattedra di studio: Serap Ejder Apay, Prof., Ataturk University
  • Cattedra di studio: Mehtap Begüm Orak, Master's student, Ataturk University

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 luglio 2026

Completamento primario (Stimato)

1 dicembre 2026

Completamento dello studio (Stimato)

1 giugno 2027

Date di iscrizione allo studio

Primo inviato

5 marzo 2026

Primo inviato che soddisfa i criteri di controllo qualità

14 giugno 2026

Primo Inserito (Effettivo)

18 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

18 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

14 giugno 2026

Ultimo verificato

1 marzo 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

INDECISO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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