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The Effect of Simulation-based Breastfeeding Education on Breastfeeding Self-efficacy and Breastfeeding Problems

Sponsor
Cukurova University (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT06081374
Collaborator
(none)
60
Enrollment
1
Location
3
Arms
12
Anticipated Duration (Months)
5
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

In the literature, there are studies conducted to determine the effect of simulation-based and different training techniques models given in the prenatal period on postpartum breastfeeding self-efficacy. However, no study was found that evaluated the effects of simulation-based and different training techniques given in the prenatal period on breastfeeding self-efficacy and breastfeeding problems. Therefore, this study was planned to determine the effect of simulation-based breastfeeding education on breastfeeding self-efficacy and breastfeeding problems in the prenatal period.

Condition or Disease Intervention/Treatment Phase
  • Device: simulation implication
 N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Supportive Care
Official Title:
Determining the Effect of Simulation-based Breastfeeding Education on Breastfeeding Self-efficacy and Breastfeeding Problems: A Randomized Controlled Study
Anticipated Study Start Date :
Nov 1, 2023
Anticipated Primary Completion Date :
Nov 1, 2024
Anticipated Study Completion Date :
Nov 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: simulation intervention

simulation will be implemented.

Device: simulation implication
Breastfeeding education is planned by dressing pregnant women with simulation models.
Other Names:
  • nursing education

    		•
    Active Comparator: education implication

    education will be implemented.

    Device: simulation implication
    Breastfeeding education is planned by dressing pregnant women with simulation models.
    Other Names:
  • nursing education

    		•
    No Intervention: control group

    no intervention will be made.

    Outcome Measures

    Primary Outcome Measures

    1. simulation affect on breastfeeding self-efficacy [postpartum 7th week]

      It is planned to increase women's breastfeeding self-efficacy through training Breastfeeding Self-efficacy scale points are supposed to be between 14-70 points. Getting higher points shows better breastfeeding self-efficacy.

    2. simulation affect on breastfeeding problems [postpartum 7th week]

      It is planned to prevent possible breast problems with the training given to women. It is supposed to get points from 18 to 90 related to Breastfeeding Experience Scale.Getting lower points is more preferable than higher points. Getting points near to 90 shows increased problems related to breastfeeding.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 45 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:

    • Pregnants between32nd-36th gestational weeks,

    • Primigravida,

    • Planning to breastfeed,

    • Can speak and understand Turkish,

    • Pregnant women who agreed to participate in the study were included.

    Exclusion Criteria:

    • Breastfeeding contraindications,

    • Having a risky pregnancy, Having received a planned breastfeeding training before,

    • Premature birth (before 37th weeks of gestation),

    • Having a systemic/chronic disease

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Seda Karaçay Yıkar Adana Sarıcam Turkey 00130

    Sponsors and Collaborators

    • Cukurova University

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    seda karaçay yıkar, Assistant professor, Cukurova University
    ClinicalTrials.gov Identifier:
    NCT06081374
    Other Study ID Numbers:
    • 123
    First Posted:
    Oct 13, 2023
    Last Update Posted:
    Oct 13, 2023
    Last Verified:
    Sep 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:
    Stillbirth

    Study Results

    No Results Posted as of Oct 13, 2023