Effect of Combined Skin-to-Skin Contact and Kangaroo Care on Breastfeeding and Bonding in Cesarean-Born Newborns

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorIstanbul University - Cerrahpasa

About this trial

This randomized controlled study aims to evaluate the effect of consecutive skin-to-skin contact applied by the mother and father on breastfeeding parameters and parent-infant bonding in babies born by cesarean section. The study includes two groups: an intervention group receiving consecutive skin-to-skin contact by the father followed by the mother, and a control group receiving routine postnatal care. Breastfeeding success and parental bonding will be assessed using validated measurement tools during the early postnatal period and follow-up.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Mothers who delivered by cesarean section

Mothers and fathers willing to participate and provide written informed consent

Newborns who are stable after birth

No health conditions in mothers or fathers that would prevent participation in skin-to-skin contact

Disqualifiers

Serious maternal or neonatal illness

Newborns requiring NICU admission

Mothers or fathers unwilling to participate

Any maternal or paternal condition preventing the implementation of skin-to-skin contact

Trial design

Design model

Parallel

Treatments tested in this trial

  • Intervention

    Behavioral

    Consecutive skin-to-skin contact is applied to newborns born by cesarean section, first by the father for 30 minutes immediately after birth, followed by skin-to-skin contact with the mother as soon as maternal clinical condition allows. Routine newborn care is provided alongside the intervention.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Consecutive Skin-to-Skin Contact Group ( İntervention )Experimental treatment 1 intervention
Group B: Routine Care Group ( Control )No intervention 0 interventions

Trial outcomes

Primary outcomes

1

Maternal Postnatal Attachment Scale (MPAS)

Maternal-infant attachment will be measured using the Maternal Postnatal Attachment Scale (MPAS). This 19-item Likert-type self-report scale assesses the mother's emotions and thoughts toward her infant.

Time frame
3 months

Secondary outcomes

1

Paternal Postnatal Attachment Scale (PPAS)

Paternal-infant attachment will be measured using the Paternal Postnatal Attachment Scale (PPAS). This 19-item scale evaluates the father's emotional approach, involvement, and interaction with the infant.

Time frame
3 months

Other outcomes

1

Bristol Breastfeeding Assessment Tool (BBAT)

Breastfeeding success will be assessed using the Bristol Breastfeeding Assessment Tool (BBAT). The tool evaluates mother-infant interaction during breastfeeding, infant positioning, latch, and sucking effectiveness, providing a systematic score of breastfeeding performance.

Time frame
3 months

Sponsors and contacts

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