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Skin-to-Skin Contact, Cheek Contact and Episiotomy Pain Control

COMPARISON OF THE EFFECTS OF SKIN-TO-SKIN CONTACT, CHEEK CONTACT AND ROUTINE CARE ON PAIN CONTROL FOLLOWING EPISIOTOMY REPAIR: A RANDOMISED CONTROLLED TRIAL

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07471724
Enrollment
155
Registered
2026-03-13
Start date
2024-04-01
Completion date
2024-11-25
Last updated
2026-03-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postpartum Pain, Episiotomy Pain, Postpartum Care

Keywords

Kangaroo care, skin to skin contact, Cheek Contact, Vaginal Birth, Postpartum Pain Management, Episiotomy

Brief summary

This randomized controlled trial aimed to evaluate the effects of skin-to-skin contact and kangaroo care on pain control during and after episiotomy repair following vaginal birth. The study was conducted at Izmir Bakircay University Cigli Regional Training and Research Hospital and included 155 healthy women who had spontaneous vaginal birth and healthy newborns. Participants were randomly assigned to three groups: kangaroo care (n=50), cheek-to-cheek contact (n=50), and standard postpartum care (n=55). Pain levels were assessed after episiotomy repair and at the 6th and 12th hours postpartum using the Verbal Rating Scale. Secondary outcomes included breastfeeding frequency and maternal satisfaction. The results indicate that kangaroo care and cheek-to-cheek contact may reduce postpartum episiotomy pain and improve breastfeeding outcomes, supporting their integration into routine maternity care.

Detailed description

This randomized controlled experimental study was conducted at Izmir Bakircay University Cigli Regional Training and Research Hospital in Türkiye. A total of 155 healthy women who had spontaneous vaginal birth at term (≥37 weeks) and their healthy newborns were included. Eligible participants were aged 18 years and older, had no medical complications, and had newborns with Apgar scores ≥7 at 1 and 5 minutes. Participants were recruited during active labour and randomly assigned to three groups: kangaroo care group (skin-to-skin contact, n=50), cheek-to-cheek contact group (n=50), and control group receiving standard postpartum care (n=55). Randomization was performed using a computer-generated random number sequence, with allocation concealed in sealed, opaque envelopes. The kangaroo care group received immediate skin-to-skin contact between mother and newborn. The cheek-to-cheek contact group received structured cheek-to-cheek contact. The control group received routine postpartum care according to hospital protocols. Primary outcomes included pain levels assessed after episiotomy repair and at the 6th and 12th hours postpartum using the Verbal Rating Scale. Secondary outcomes included breastfeeding frequency, amount of local anesthesia used, and maternal satisfaction. Data were collected using structured questionnaires on sociodemographic and obstetric characteristics. Statistical analyses were performed using descriptive statistics, chi-square tests, one-way ANOVA, and Bonferroni post-hoc tests. All participants provided written informed consent prior to participation. The study was approved by the Izmir Bakircay University Non-Interventional Clinical Research Ethics Committee and conducted in accordance with the Declaration of Helsinki.

Interventions

Immediately after vaginal birth and during episiotomy repair, the newborn was placed prone on the mother's bare chest to provide continuous skin-to-skin contact. The infant was positioned in an upright and safe posture and covered with a blanket when necessary. The intervention was maintained according to the study protocol and supervised by trained midwives.

BEHAVIORALCheek-to-Cheek Contact

During and after episiotomy repair, structured cheek-to-cheek contact was established between the mother and the newborn. The infant's cheek was gently placed in contact with the mother's cheek in a comfortable position. The procedure was applied according to standardized instructions and supervised by trained staff.

Sponsors

Ege University
Lead SponsorOTHER
Izmir Bakircay University
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

This study was designed as a three-arm, parallel-group randomized controlled trial. Eligible participants were randomly assigned during active labour to receive kangaroo care, cheek-to-cheek contact, or standard postpartum care. Outcomes were assessed after episiotomy repair and during the early postpartum period.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Women aged 18 years or older Able to speak and understand Turkish Singleton pregnancy at ≥37 gestational weeks Spontaneous vaginal birth with mediolateral episiotomy Mother and newborn clinically stable after birth Newborn APGAR score ≥7 at 1 and 5 minutes Willingness to participate and provision of informed consent

Exclusion criteria

* Operative vaginal birth (vacuum or forceps) Third- or fourth-degree perineal tear or extensive perineal laceration Epidural analgesia during labor Maternal or neonatal complications requiring medical intervention Conditions requiring maternal-infant separation after birth Refusal to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
Episiotomy pain intensity (Numeric Rating Scale)Immediately after episiotomy repair, at 6 hours postpartum, and at 12 hours postpartumMaternal pain intensity related to episiotomy repair measured using a 0-10 Numeric Rating Scale (NRS), where 0 indicates no pain and 10 indicates worst possible pain. Pain scores were self-reported by mothers during follow-up assessments.

Secondary

MeasureTime frameDescription
Breastfeeding frequencyWithin first 12 hours postpartumNumber of breastfeeding episodes during early postpartum period
Newborn APGAR scores1st and 5th minute after birthAPGAR scores at 1 and 5 minutes after birth

Countries

Turkey (Türkiye)

Contacts

PRINCIPAL_INVESTIGATORAysun Ekşioğlu, Associate Professor

Ege University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 14, 2026