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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT06081374
Other study ID # 123
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date November 1, 2023
Est. completion date November 1, 2024

Study information

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

Clinical Trial 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.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 60
Est. completion date November 1, 2024
Est. primary completion date November 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Device:
simulation implication
Breastfeeding education is planned by dressing pregnant women with simulation models.

Locations

Country Name City State
Turkey Seda Karaçay Yikar Adana Saricam

Sponsors (1)

Lead Sponsor Collaborator
Cukurova University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary simulation affect on breastfeeding self-efficacy 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. postpartum 7th week
Primary simulation affect on breastfeeding problems 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. postpartum 7th week