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Effect of Breastfeeding Training Program and System (BMUM) for Mothers

Effect of Breastfeeding Training Program and Nurse-led Breastfeeding Online Counselling System (BMUM) for Mothers: Randomized Controlled Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05781477
Enrollment
72
Registered
2023-03-23
Start date
2020-06-20
Completion date
2022-07-15
Last updated
2023-03-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breastfeeding

Brief summary

The goal of the study was to investigate effect of breastfeeding training program and nurse-led breastfeeding online counselling system (BMUM) on mothers' breastfeeding self-efficacy, breastfeeding attitudes, breastfeeding problems and postpartum depression we hypothesized that there would be differences between BG and CG groups in terms of breastfeeding self-efficacy, breastfeeding problems, postpartum depression and breastfeeding frequency. This was a randomized controlled trial. Participants were randomly assigned to the breastfeeding group (BG; n = 36), or control group (CG; n = 36). Control group will receive only standart care breastfeeding group will receive standart care and web based breastfeeding support. Breastfeeding attitudes, infant feeding attitude breastfeeding problems and postpartum depression will assessment. The assesment point will be 32-37 gestational week, postpartum 1st day, 1st week, 3 months, and 6 months.

Interventions

BEHAVIORALBmum supportive system

Bmum is a web-based online tracking system that aims to improve positive attitude about breastfeeding

Sponsors

Kastamonu University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* 18-35 years old, * Primipara with a singleton pregnancy * 32- and 37-weeks of gestation, * Willingness to participate in the workshop program

Exclusion criteria

* Having a chronic illness * Having pre-term labor or an abnormal fetal screening * Had a psychiatric disorder or anxiety disorder * Having any other high-risk complications

Design outcomes

Primary

MeasureTime frameDescription
Breastfeeding Self efficacy change on five points between groups32-37 weeks 1st. day 1. week 3rd months 6th monthsBreastfeeding Self efficacy short form scale will use to assessment breasfeeding self efficacy. Total scores vary from 14 to 70, with higher scores indicating greater self-efficacy
Infant feeding attitude change on five points between groups32-37 weeks 1st. day 1. week 3rd months 6th monthsIowa Infant Feeding Attitude Scale (IIFAS) will use to assessment infant feeding attitude Higher scores indicate a more favorable attitude toward newborn feeding
Postpartum depression change on four points between groups.1st. day 1st. week 3rd months 6th monthsEdinburgh Postnatal Depression Scale (EPDS) will use to assesment postpartum depression. The total score ranges from 0 to 30, with higher scores suggesting a higher level of depression symptoms.
breast problems between two groups on 1 st week1st weekbreast problem will assesment with breastfeeding problems questionnaire. number and percent will use to evaluate.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026