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Women (Between 18 to 50 Years Old)NCT07458789

Breastfeeding Education

A study testing Pecha Kucha in people with Women (Between 18 to 50 Years Old) and Breastfeeding Self-Efficacy, run by Cukurova University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This study was designed to determine the effect of breastfeeding education given to primiparous pregnant women using the pecha kucha technique on breastfeeding self-efficacy and maternal bonding. The research is a randomized controlled experimental study. Read more about this study

Who is it for?
Ages 18 years and older, women onlyHealthy volunteers can take part
What is being tested?
Pecha Kucha
Could I receive a placebo?
No, everyone receives an active treatment
How many people
84 participants
Where
1 siteTurkey (Türkiye)
Study dates
10 Mar 2026to 16 Jun 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Women only
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Primiparous
  • 32 weeks or more of pregnancy
  • Being over 18 years old

Who cannot join

  • High-risk pregnancy
  • Multiparous

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Cukurova university

    Adana, Adana, 01330

Other trials in Turkey (Türkiye)

About this study

Official title: The Effect of Breastfeeding Education Given to Primiparous Pregnant Women Using the Pecha Kucha Technique on Breastfeeding Self-efficacy and Maternal Attachment: a randomızed Controlled Experimental Study

This study was designed to determine the effect of breastfeeding education given to primiparous pregnant women using the pecha kucha technique on breastfeeding self-efficacy and maternal bonding. The research is a randomized controlled experimental study.

Read the detailed description

The study population will consist of primiparous pregnant women in their third trimester who apply to the obstetrics and gynecology outpatient clinics of state hospitals. The sample will consist of primiparous pregnant women who volunteer to participate in the study. Data will be collected through face-to-face interviews. A personal information form, the "Maternal Attachment Scale," and the "Prenatal Breastfeeding Self-Efficacy Scale" will be used to collect data.

Being tested
Pecha Kucha

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Pecha KuchaBehavioural

    Also called Control group

    Showing textless images in a 20-second sequence over 20 slides.

Study groups in NCT07458789
Study groupRoleWhat they receive
Pecha KuchaExperimentalShowing textless images in a 20-second sequence over 20 slides.
Receives: Behavioral: Pecha Kucha
control groupActive comparatorParticipants in this group will receive breastfeeding education using the traditional PowerPoint presentation method.
Receives: Behavioral: Pecha Kucha

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Maternal Attachment Inventory

    The Maternal Attachment Inventory (MAI) was developed by Mary E. Muller in 1994 to measure maternal attachment through love. Muller tested maternal adaptation and maternal attachment in two phases using Mercer's theory of maternal role adaptation. The Cronbach's alpha value of the MAI is 0.77 for mothers with one-month-old babies and 0.82 for mothers with four-month-old babies. The validity and reliability of the scale in Turkey were established by Kavlak and Şirin (2009). This study was methodologically planned to adapt the Maternal Attachment Inventory to the Turkish population and test its validity and reliability on mothers with one- and four-month-old babies. Each item is a 26-item scale with a 4-point Likert scale ranging from "always" to "never". Each item includes direct statements and is scored as follows: always (a)=4 points, frequently (b)=3 points, sometimes (c)=2 points, and never (d)=1 point. The lowest possible score on the scale measuring maternal feelings and behavior

    Measured: up to 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 Mar 2026
  2. Study start10 Mar 2026
  3. Primary completion15 Jun 2026
  4. Study completion16 Jun 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Investigator
Enrolment
84 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07458789
Sponsor's protocol ID
Balcalı
Status last verified
Jun 2026
First submitted
19 Feb 2026
Last updated
22 Jun 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Pecha Kucha in people with Women (Between 18 to 50 Years Old) and Breastfeeding Self-Efficacy, run by Cukurova University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 22 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Maternal Attachment Inventory (time frame: up to 12 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Jun 2026.

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