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The Effect of a Web-Based Breastfeeding Education Program for Adolescent Pregnant

Y

Yuzuncu Yıl University

Status

Completed

Conditions

Breastfeeding

Treatments

Behavioral: web based education

Study type

Interventional

Funder types

Other

Identifiers

NCT06732076
WEB TABAN

Details and patient eligibility

About

It is crucial to prepare adolescent mothers-who represent a vulnerable group where the importance of breastfeeding is increasingly emphasized-for the breastfeeding process. One potential method for promoting breastfeeding is through web-based education interventions. The aim of this study was to evaluate the effect of a web-based breastfeeding education program, developed by the researchers, on breastfeeding outcomes among adolescent pregnant women in the postpartum period. This randomized controlled study involved a sample of 100 pregnant adolescents, aged 15-19 years, who were in their third trimester of pregnancy. The study commenced after obtaining ethical approval and permissions from the hospital where the research was conducted.

A web-based breastfeeding education program was administered to the experimental group. Data were collected using a Socio-Demographic Data Form, the Breastfeeding Self-Efficacy Scale Short Form (Antenatal Version), the Breastfeeding Self-Efficacy Scale Short Form (Postnatal Version), and the LATCH Breastfeeding Diagnosis and Assessment Scale. Data collection occurred during the third trimester (pretest) and the 1st and 8th postnatal weeks (posttest).

Enrollment

90 patients

Sex

Female

Ages

15 to 19 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Aged between 15 and 19 years
  • Had not previously received planned breastfeeding education
  • Were between 28 and 37 weeks gestation (third trimester)
  • Gave birth at term
  • Had no health issues preventing breastfeeding
  • Could read, write, and respond to questions
  • Had access to a computer, tablet, or smartphone, and had regular internet access.

Exclusion criteria

  • Participants were excluded if they had multiple pregnancies
  • Physical or mental health problems, communication disabilities
  • A history of breast surgery
  • İf their newborns were considered high-risk.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

90 participants in 2 patient groups

experimental
Experimental group
Description:
web based education
Treatment:
Behavioral: web based education
control
No Intervention group
Description:
no intervention

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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