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Clinical Trials/NCT06199245
NCT06199245
Recruiting
Not Applicable

The Effect of Emotional Freedom Technique on Breastfeeding Success and Self-Efficacy in Primiparous Women in the Early Postpartum Period Who Had a Cesarean Delivery

Medipol University1 site in 1 country60 target enrollmentStarted: November 1, 2023Last updated:

Overview

Phase
Not Applicable
Status
Recruiting
Sponsor
Medipol University
Enrollment
60
Locations
1
Primary Endpoint
Bristol Breastfeeding Rating Scale

Overview

Brief Summary

This study was planned to determine the effect of emotional freedom technique (EFT) on breastfeeding success and self-efficacy in primiparous women in the early postpartum period who had a cesarean delivery.

Detailed Description

Breast milk is an easily digestible, natural food that reduces the morbidity and mortality of the newborn and contains the fluid, energy and nutrients necessary for its physical, spiritual and mental development. Breastfeeding not only has a biological effect on the mother and baby, but also has an emotional effect and has many immunological, psychological, social and economic benefits for both mother and baby. Therefore, it is of great importance that the baby be fed exclusively with breast milk for the first 6 months and that breastfeeding continues until the age of 2.

EFT, a needle-free and emotional form of acupuncture, is an energy technique that emerged from the idea that "The cause of all negative emotions is the disruption in the body's energy system." EFT; It can be safely applied to individuals of all ages, including the elderly, pregnant women and children. When looking at the literature, no studies were found regarding breastfeeding and EFT. It has been observed that primiparous women, especially those who have had a cesarean section, have difficulty breastfeeding. It is thought that breastfeeding will be reinforced and improved with EFT, which helps to eliminate negative emotions in the subconscious and create a positive mood.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Single (Participant)

Masking Description

The researcher knows the distribution of the groups, but the participants do not know whether they are in the experimental or control group.

Eligibility Criteria

Ages
18 Years to 35 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Being between the ages of 18-35,
  • Primiparous and giving birth by cesarean section,
  • Having a spontaneous pregnancy,
  • Wound, scar, infection etc. in the tapping area. without conditions,
  • Women who do not have verbal communication problems

Exclusion Criteria

  • Being outside the age range of 18-35
  • Has any problem that prevents communication,
  • Those who gave birth normally
  • Having had a high-risk pregnancy,
  • Women who want to leave the study

Outcomes

Primary Outcomes

Bristol Breastfeeding Rating Scale

Time Frame: one day

This scale measures breastfeeding success. The scale is a Likert-type scale consisting of 4 items: "positioning", "holding", "sucking" and "swallowing". Each item is scored between 0-2 points. The lowest score from the scale is 0, the highest score is 8. Low scores indicate that breastfeeding is not effective, while high scores indicate that breastfeeding is effective.

Secondary Outcomes

  • Subjective Units of Disturbance Scala(one day)
  • breastfeeding self-efficacy scale(one day)

Investigators

Sponsor
Medipol University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Eda Yuzuguler

Msc student

Medipol University

Study Sites (1)

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