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

NCT ID: NCT06081374

Last Updated: 2023-10-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-11-01

Study Completion Date

2024-11-01

Brief Summary

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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.

Detailed Description

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Conditions

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Postpartum Complication Caesarean Section;Stillbirth

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Participants

Study Groups

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simulation intervention

simulation will be implemented.

Group Type EXPERIMENTAL

simulation implication

Intervention Type DEVICE

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

education implication

education will be implemented.

Group Type ACTIVE_COMPARATOR

simulation implication

Intervention Type DEVICE

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

control group

no intervention will be made.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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simulation implication

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

Intervention Type DEVICE

Other Intervention Names

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nursing education

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Cukurova University

OTHER

Sponsor Role lead

Responsible Party

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seda karaçay yıkar

Assistant professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Seda Karaçay Yıkar

Adana, Sarıcam, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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123

Identifier Type: -

Identifier Source: org_study_id

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