The Effect of Skin-to-skin Contact at Birth

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorGaziantep Islam Science and Technology University

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Vaginal delivery

Primiparous pregnancy

Delivery at 37 weeks or later

Single, live fetus

Disqualifiers

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,

Trial design

Design model

Parallel

Treatments tested in this trial

  • Immediate skin-to-skin contact after birth (intervention group)

    Other intervention

    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.

Treatment groups

96 Participants
are divided into 2 treatment groups
Group A: Control groupNo intervention 0 interventions
Group B: Immediate Skin-to-Skin Contact After Birth (intervention group)Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Personal Information Form

The form prepared by the researchers consists of 14 questions about the mothers' socio-demographic characteristics, obstetric characteristics, and newborns.

Time frame
baseline
2

Breastfeeding Motivation Scale

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.

Time frame
Periprocedural
3

VAS

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).

Time frame
Periprocedural
4

Postnatal Parenting Behavior Scale

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.

Time frame
Periprocedural

Secondary outcomes

Other outcomes

Sponsors and contacts

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