Actively Recruiting

Phase Not Applicable
Age: 18Years - 40Years
FEMALE
Healthy Volunteers
NCT06252311

The Effect of Mindfulness-Based Breastfeeding Programme in Mothers After Cesarean Delivery

Led by Akdeniz University · Updated on 2025-07-29

140

Participants Needed

2

Research Sites

78 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The study is a randomised controlled trial designed to determine the effect of the Mindfulness-Based Breastfeeding Programme on maternal breastfeeding awareness, breastfeeding attitudes and breastfeeding continuation among mothers who have given birth by caesarean section. The study will evaluate the effectiveness of the Mindfulness-Based Breastfeeding programme using the "Mindful Breastfeeding Scale" and "Iowa Infant Feeding Attitude Scale". The research will use stratified and simple randomisation methods. Research data will be collected from mothers who gave birth by caesarean section at the gynaecology clinic of the Afyonkarahisar Health Sciences University Health Application and Research Center of between April 2024 and December 2025.

CONDITIONS

Official Title

The Effect of Mindfulness-Based Breastfeeding Programme in Mothers After Cesarean Delivery

Who Can Participate

Age: 18Years - 40Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Be between the ages of 18 and 40 years
  • Have had a caesarean section at 37 weeks or more of gestation
  • Be hospitalized at Afyonkarahisar Health Sciences University Health Application and Research Center, Gynaecology and Obstetrics Clinic
  • Have a single, healthy baby (no multiple pregnancy)
  • Have completed at least primary school education
  • Be able to communicate in Turkish by phone using the WhatsApp application
  • Have the baby with the mother
Not Eligible

You will not qualify if you...

  • Have a high-risk pregnancy
  • Have a medical condition or take medication that prevents breastfeeding
  • Have communication problems such as vision, hearing, speech, or language difficulties
  • Have a psychiatric illness
  • Have had a hysterectomy after caesarean section
  • Have an obstacle preventing the baby from being with the mother or if the baby is in the neonatal intensive care unit
  • Have a condition or disease that prevents mindfulness practices like breathing exercises or body scanning

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Afyonkarahisar Health Sciences University Health Application and Research Center

Afyonkarahisar, Dörtyol, Turkey (Türkiye), 03030

Not Yet Recruiting

2

AFSU Health Research and Application Center

Afyonkarahisar, Merkez, Turkey (Türkiye)

Actively Recruiting

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Research Team

S

Serife BUYUKOKUDAN

CONTACT

O

Oznur KORUKCU

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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