Skip to main content
Clinical Trials/NCT05781477
NCT05781477CompletedNot Applicable

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

Kastamonu University2 sites in 1 country72 target enrollmentStarted: June 20, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
72
Locations
2
Primary Endpoint
Infant feeding attitude change on five points between groups

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to 35 Years (Adult)
Sex
Female
Accepts 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

Arms & Interventions

Bmum GROUP

Experimental

Mothers in this group were given supportive breastfeeding support with web based

Intervention: Bmum supportive system (Behavioral)

control group

No Intervention

Mothers in the control and intervention groups were given standard care based on the Baby-Friendly Hospital Intervention Standard.

Outcomes

Primary Outcomes

Infant feeding attitude change on five points between groups

Time Frame: 32-37 weeks 1st. day 1. week 3rd months 6th months

Iowa 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.

Time Frame: 1st. day 1st. week 3rd months 6th months

Edinburgh 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.

Breastfeeding Self efficacy change on five points between groups

Time Frame: 32-37 weeks 1st. day 1. week 3rd months 6th months

Breastfeeding 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

breast problems between two groups on 1 st week

Time Frame: 1st week

breast problem will assesment with breastfeeding problems questionnaire. number and percent will use to evaluate.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Şahika ŞİMŞEK ÇETİNKAYA

PhD,Dr.

Kastamonu University

Study Sites (2)

Loading locations...

Similar Trials