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Breast Milk and Breastfeeding Education Given in the Antenatal Period (BSES-SF)

B

Bursa Uludag University

Status

Completed

Conditions

Breastfeeding

Treatments

Other: breastfeeding education

Study type

Interventional

Funder types

Other

Identifiers

NCT04757324
Breastfeeding Education

Details and patient eligibility

About

We aimed to examine the influence of breast milk and breastfeeding education given in the ante-natal period on LATCH score and breastfeeding self-efficacy score.

Full description

Practices for increasing breastfeeding self-efficacy are of vital importance and they increase the level of breastfeeding self-efficacy. Breast milk and breastfeeding educations have given in the ante-natal period are another way of increasing the success of breastfeeding.

In this experimental investigation, 80 pregnant women who attended a baby-friendly hospital were randomly assigned to the education (n = 40) or control (n = 40) groups. The pregnant women in the intervention group received 4 hours of human milk and breastfeeding educational sessions along with routine care and furthermore, a brochure prepared by the researcher was given. All women whose estimated delivery date had approximated were questioned about whether they had given birth or not, and the sociodemographic data form, the LATCH Breastfeeding Assessment Tool and the Breastfeeding Self-efficacy Scale-short form were applied to the subjects in the education and the control group by visiting them at home when the post-partum first week had been completed.

Enrollment

67 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

inclusion criteria Being above 18 years of age, Having completed the 26th gestational week (At training phase), Having no problem with vision and hearing, Having no disease that can prevent breastfeeding, Having a pregnancy with no risk, Having no systemic disease, Planning to breastfeed after birth

excusion criteria the mother stops researching. treating the baby in neonatal intensive care

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

67 participants in 2 patient groups

education arm
Experimental group
Description:
Breastfeeding training was given to the training arm
Treatment:
Other: breastfeeding education
control arm
No Intervention group
Description:
Breastfeeding training not given to control arm

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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