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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05781477
Other study ID # 4-6/16.06.2020
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 20, 2020
Est. completion date July 15, 2022

Study information

Verified date March 2023
Source Kastamonu University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 72
Est. completion date July 15, 2022
Est. primary completion date November 20, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 35 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
Turkey Kastamonu University Merkez Kastamonu
Turkey Sahika Simsek Çetinkaya Merkez Kastamonu

Sponsors (1)

Lead Sponsor Collaborator
Kastamonu University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Breastfeeding Self efficacy change on five points between groups 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 32-37 weeks 1st. day 1. week 3rd months 6th months
Primary Infant feeding attitude change on five points between groups Iowa Infant Feeding Attitude Scale (IIFAS) will use to assessment infant feeding attitude Higher scores indicate a more favorable attitude toward newborn feeding 32-37 weeks 1st. day 1. week 3rd months 6th months
Primary Postpartum depression change on four points between groups. 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. 1st. day 1st. week 3rd months 6th months
Primary breast problems between two groups on 1 st week breast problem will assesment with breastfeeding problems questionnaire. number and percent will use to evaluate. 1st week
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