NCT06528782

Brief Summary

To evaluate the effect of breastfeeding education given with Pecha Kucha method in the prenatal period on breastfeeding self-efficacy, infant feeding attitude and breastfeeding satisfaction in the postpartum period.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
75

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jul 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 11, 2024

Completed
14 days until next milestone

First Submitted

Initial submission to the registry

July 25, 2024

Completed
5 days until next milestone

First Posted

Study publicly available on registry

July 30, 2024

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 11, 2024

Completed
4 days until next milestone

Study Completion

Last participant's last visit for all outcomes

September 15, 2024

Completed
Last Updated

September 25, 2024

Status Verified

September 1, 2024

Enrollment Period

2 months

First QC Date

July 25, 2024

Last Update Submit

September 23, 2024

Conditions

Keywords

Breast FeedingMidwiferyBreast Feeding Education

Outcome Measures

Primary Outcomes (1)

  • Antenatal and Pospartum Breastfeeding Self-Efficacy Scale Short Form

    The scale can be administered in prenatal and postnatal periods and measures how competent women feel about breastfeeding. The items of the five-point Likert-type scale are scored as not at all sure, not very sure, sometimes sure, sure, very sure. The lowest score that can be obtained from all the evaluation scores of the scale is 14 and the highest score is 70. A low total score on the scale indicates a low perception of breastfeeding self-efficacy. In the original scale, the Cronbach's alpha reliability coefficient of the prenatal form was 0.87 and the Cronbach's alpha reliability coefficient of the postnatal form was 0.86.

    0,2 and 4 weeks

Secondary Outcomes (2)

  • Infant Feeding Attitude Scale (IOWA)

    0,2 and 4 weeks

  • Visual Assessment Scale - Satisfaction (VAS - S)

    2 and 4 weeks

Study Arms (2)

Pecha Kucha Group

EXPERIMENTAL

Pregnant women who meet the inclusion criteria assigned to the Pecha Kucha group will be informed about the study and their written and verbal consent will be obtained. Pregnant women will be asked to fill out the 'Introductory Characteristics Information Form', the 'Antenatal Breastfeeding Self-Efficacy Scale Short Form' and the 'Infant Feeding Attitude Scale (IOWA)' before the training at the first encounter, and then breastfeeding training prepared by the Pecha Kucha method will be given. 2 weeks after the training, she will be followed up by phone and asked to answer the Pospartum Breastfeeding Self-Efficacy Scale Short Form, Infant Feeding Attitude Scale (IOWA) and Visual Comparison Scale Satisfaction (VAS-M) scale. 4 weeks after the training, she will be asked to answer the Pospartum Breastfeeding Self-Efficacy Scale Short Form, Infant Feeding Attitude Scale (IOWA) and Visual Comparison Scale Satisfaction (VAS-M) scale.

Other: Pecha Kucha method

Control Group

NO INTERVENTION

Pregnant women who meet the inclusion criteria and who are assigned to the control group will be informed about the study and their written and verbal consent will be obtained. Pregnant women will be asked to fill out the 'Descriptive Characteristics Information Form', 'Antenatal Breastfeeding Self-Efficacy Scale Short Form' and 'Infant Feeding Attitude Scale (IOWA)' at the first encounter. After 2 weeks, she will be followed up by telephone and asked to answer the Pospartum Breastfeeding Self-Efficacy Scale Short Form, Infant Feeding Attitude Scale (IOWA) and Visual Comparison Scale Satisfaction (VAS-M). After 4 weeks, she will be asked to answer the Pospartum Breastfeeding Self-Efficacy Scale Short Form, Infant Feeding Attitude Scale (IOWA) and Visual Comparison Scale Satisfaction (VAS-M).

Interventions

The Pecha Kucha method will be prepared in the form of a presentation consisting of 20 slides each shown for 20 seconds. The Pecha Kucha presentation lasts 6 minutes and 40 seconds, and most slides present only images. This method is planned to be used in breastfeeding education as it will be more memorable because it contains more visual, auditory and short information.

Pecha Kucha Group

Eligibility Criteria

Age18 Years - 60 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsPregnant women 38 weeks and over
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Volunteered to participate in the research,
  • To be able to speak and understand Turkish,
  • Over 18 years of age,
  • At least primary school graduate,
  • Gestational week 38 weeks and above
  • No chronic illness,
  • Pregnant women without communication barriers will be included in the study.

You may not qualify if:

  • Have a medical indication that prevents breastfeeding,
  • Multiple pregnancies,
  • A person with a mental illness,
  • Not wanting to continue the research process,
  • The one who still hasn't given birth 2 weeks after the training,
  • Not having their baby with them after childbirth,
  • Pregnant women who cannot be reached during the follow-up period will be excluded from the study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ankara Etlik City Hospital

Ankara, Ankara, 6010, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Breast Feeding

Condition Hierarchy (Ancestors)

Feeding BehaviorBehavior

Study Officials

  • Zehra Bicav

    Saglik Bilimleri Universitesi

    PRINCIPAL INVESTIGATOR
  • Filiz Ünal Toprak, PhD

    Saglik Bilimleri Universitesi

    PRINCIPAL INVESTIGATOR
  • Ceren Ceyda İşbuğa

    Ankara Etlik City Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Masking Details
Since the application will be performed by the researcher, patients will be blinded in this study. The statistician will be blinded in the evaluation of the data.
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: Two groups with pecha kucha group and control group
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

July 25, 2024

First Posted

July 30, 2024

Study Start

July 11, 2024

Primary Completion

September 11, 2024

Study Completion

September 15, 2024

Last Updated

September 25, 2024

Record last verified: 2024-09

Data Sharing

IPD Sharing
Will not share

Locations