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Effect of Oketani Breast Massage on Promoting Breastfeeding

NCT07354360 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2026-02
Last updated
2026-03-10

Condition(s) studied

BreastfeedingBreastfeeding Self-EfficacyOketani MassageLatching

Investigational drug(s) / intervention(s)

Oketani massage group

Oketani massage group: primipara who meet inclusion criteria and who are assigned to the intervention group will be informed about the study and their consent will be obtained.. Primipara mothers in the intervention group will receive Oketani massage after delivery to enhance successful breastfeeding. The massage is performed using 8 specific hand steps (7 steps for separating the mammary glands and 1 step for expression). Each session lasts 15-20 minutes and is repeated according to the study protocol. the researcher will train primipara relatives to apply Oketani massage after discharge to primipara after discharge. The massage aims to increase milk flow, reduce breast engorgement, improve breast softness, enhance nipple elasticity, and increase maternal comfort and breastfeeding self-efficacy.

Study summary

Breastfeeding is essential for infant survival and maternal health; however, many primipara women experience breastfeeding difficulties in the early postpartum period, particularly, latching difficulties, ineffective milk transfer, low breastfeeding self-efficacy and breast engorgement, which may compromise successful breastfeeding. Oketani massage is a non-pharmacological, cost-effective breast massage technique developed to enhance milk flow, improve maternal comfort during breastfeeding and reduce breast engorgement. This study aims to evaluate effect of Oketani massage on successful breastfeeding. Successful breastfeeding will be assessed through indicators of maternal latching technique, successful breastfeeding behavior and maternal breastfeeding self-efficacy. The findings of this study may support the use of Oketani massage as a supportive nursing intervention to promote successful breastfeeding outcomes in the early postpartum period

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
35 Years
Healthy volunteers
No
inclusion criteria: 1. Age between 18 and 35 years 2. Singleton pregnancy 3. Term gestation (\>37-40 weeks). 4. Women willing to breast feed 5. The woman will deliver by cesarean section and has relative with her 6. Absence of maternal physical and/ or mental illness that prevents breastfeeding. The exclusion criteria include: 1. Women with breast problems such as breast tumors, breast surgery and nipple problems 2. Women have obstetric complications as postpartum hemorrhage. 3. Neonatal problems

Primary outcome measure(s)

  • The LATCH Assessment sheet — baseline; 2nd time after the 1st six hours after birth and the third time on discharge(24 hours postpartum)
    It will be adopted from (Jensen et al, 1994) to assess primipara women's need for breastfeeding support, it is numbered from zero to ten, and getting a score of less than ten offers the women's need for more support during breastfeeding. The letters of the acronym LATCH appoint separate areas of assessment: L (Latch) for how well the infant latches onto the breast; A (Audible swallowing) refers the amount of audible swallowing noted while nursing the neonate; T (Type of nipple) for the women's nipple type; C (Comfort) for the women's level of comfort regarding the breast and nipple; and H (Hold) indicates to whether or not the women need help in positioning the infant. Scoring system: The system assigns a numerical score, 0, 1, or 2, to five key statements. LATCH score of poor (0 to 3), moderate (4 to 7), and good (8 to 10)

Trial sites (1)

FacilityCityRegionStatus
Mansoura University Al Mansurah Egypt
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07354360 on ClinicalTrials.gov ↗ ← All trials in Egypt