CClinicalTrials.gg
CompletedNCT05950048Updated Nov 28, 2023

THE EFFECT OF WEB-BASED BREASTFEEDING COUNSELING

An interventional study of The web-based breastfeeding counseling in Web-based Breastfeeding Counseling, sponsored by Mersin University. Completed at 1 site in Turkey. Open to female participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-11-28.

Sponsored by Mersin University · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 6 months after the study started (first participant enrolled Jan 2023, registered Jul 2023).
Phase
Not applicable
Study type
Interventional
Enrollment
66
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
Female
01

Study summary

This randomized controlled study evaluates the effect of Web-Based Breastfeeding Counseling given to mothers on breastfeeding exclusively with breast milk in the first 6 months, breastfeeding motivation and breastfeeding problems.The main hypotheses it aims to answer are:

  1. The web-based breastfeeding counseling given to the mothers in the experimental group is effective on the breastfeeding only for the first six months.
  2. The web-based breastfeeding counseling given to the mothers in the experimental group is effective on the breastfeeding motivation of the mothers.
  3. The web-based breastfeeding counseling given to the mothers in the experimental group is effective on the breastfeeding problems of the mothers.
Read the detailed description

In the study, 66 mother will randomly assigned to web-based breastfeeding counseling/experimental group and control group. To the web-based breastfeeding counseling/experimental group (n =33), during the first 6 months after birth, they will be directed to the web-based breastfeeding consultancy website. On this page, mothers will receive counseling on breastfeeding (written, visual, audio materials and telephone counseling) from birth. On the other hand, no other intervention will be applied to the control group other than routine treatment and midwifery care. The primary outcome of the research is the effect of web-based breastfeeding counseling on the breastfeeding only for the first six months of mothers. The secondary outcome of the study is to determine the effect of web-based breastfeeding counseling on the breastfeeding motivation of the mothers. The tertiary outcome of the study is to determine the effect of web-based breastfeeding counseling on the breastfeeding problems of the mothers.

02

Conditions studied

  • Web-based Breastfeeding Counseling

Keywords

  • Breastfeeding counseling
  • Breastfeeding motivation
  • Web-based
  • Breast milk
  • Breastfeeding problems
03

In context

Lead sponsor

Mersin University is the lead sponsor of 173 studies on the registry; 48 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

  • treated at the relevant hospital
  • who volunteered to participate in the research
  • in the age range of 18-40
  • oriented to place, time and person
  • 37-42 weeks of pregnancy. between the weeks
  • having first pregnancy
  • having a healthy pregnancy
  • Those who do not have any health problems that prevent breastfeeding (HIV, drug use, etc.)
  • who is literate
  • able to use computer or smart phone
  • Those who do not have a communication barrier (not knowing Turkish, mental retardation, etc.)
  • with internet at home

Exclusion criteria

Exclusion Criteria:

  • any health problem that prevents breastfeeding
  • having a baby with any health problem that prevents breastfeeding
  • who have a baby who was taken to the intensive care unit due to postpartum health problems
  • with multiple pregnancy
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
66 participants (actual)

Study arms

  • Experimental
    Web-based breastfeeding counseling/experimental group

    The web-based breastfeeding counseling/experimental group (n =33) will be given the web-based breastfeeding counseling.

    Other: The web-based breastfeeding counseling

  • No intervention
    Control group

    It will only take routine treatment and midwifery care.

Interventions

  • OtherThe web-based breastfeeding counseling

    To the web-based breastfeeding counseling/experimental group (n =33), during the first 6 months after birth, they will be directed to the web-based breastfeeding consultancy website. On this page, mothers will receive counseling on breastfeeding (written, visual, audio materials and telephone counseling) from birth. In addition, the Web-based breastfeeding counseling/experimental group will fill out data collection forms in the first 24 hours, 1st, 2nd, 4th and 6th months after delivery.

06

What researchers measure

Primary outcomes

  1. Postpartum Breastfeeding Evaluation and Follow-up Form

    In this form, which was created by the researchers to evaluate and monitor postpartum breastfeeding, using the literature, there are questions that evaluate situations such as "the way babies are fed, the status of giving additional nutrients other than breast milk, the mothers' breastfeeding problems, and the mother's desire to continue breastfeeding.

    Time frame: Change from before implementation (within the first 24 hours postpartum) and 1st, 2nd, 4rd and 6th months postpartum

Secondary outcomes

  1. Breastfeeding Motivation Scale

    It was developed by Kestler, Peleg et al (2015) and adapted into Turkish by Mızrak and Özerdoğan (2017). The scale consists of 24 items in total and consists of 5 sub-dimensions: "Integrated regulation" "intrinsic motivation and identified regulation", "introjected regulation - social approval", "introjected regulation - social pressure", and "external regulation - additional benefits".The Cronbach alpha value of the scale was found to be 0.855. Cronbach's alpha values for sub-dimensions vary between (0.846 - 0.670). The scale is in 4-point Likert type, and each item is scored between 1-4 (from 1 = "I strongly disagree" to 4 = "I totally agree"). The scale does not have a total score. The scores of the sub-dimensions are calculated by taking the average of the sub-dimension scores of the scale. As the score obtained from the scale sub-dimension increases, the motivation to breastfeed, which represents that sub-dimension, also increases.

    Time frame: Change from before implementation (within the first 24 hours postpartum) and 1st, 2nd, 4rd and 6th months postpartum

  2. Breastfeeding Problems Assesment Scale

    It was developed by Wambach (1990), is a 30-item scale in order to determine the level of the problem experienced ("never happened" (1) to "unbearably happened" (5)). The total score of the scale varies between 18 and 90. A high score indicates that the severity of the problem has increased. The 18 items in the scale include mechanical concerns, process concerns, concerns about milk insufficiency , concerns about the udder and questions related to social concerns. The last 12 items of the scale evaluate whether breastfeeding is continued, whether formula is added, how often formula is given, and what are the breastfeeding difficulties related to the mother's decision to wean in case of early weaning. The Turkish validity and reliability of the scale was performed by Uyanık (2019) and he Cronbach's alpha value of the scale was found to be 0.77 for the sub-dimensions, and between 0.71-0.85.

    Time frame: Change from before implementation (within the first 24 hours postpartum) and 1st, 2nd, 4rd and 6th months postpartum

07

Study locations

1 site
  • Mersin University
    Mersin, 33343, Turkey
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 28, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05950048
Lead sponsor
Mersin University
Responsible party
Ayşe Gül KOCA (Midwife, Mersin University) — Principal investigator
First posted
Jul 18, 2023
Start date
Jan 1, 2023
Primary completion
Nov 25, 2023
Completion
Nov 25, 2023
Last update
Nov 28, 2023

Study contacts

Mine YURDAKUL, Doctorate
study director · Mersin University

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Nov 2023. You cannot join it, but the record below documents what was studied.

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