Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 11:34 PM
Ignite Modification Date:
2025-12-24 @ 11:34 PM
NCT ID:
NCT06277856
Eligibility Criteria:
Mothers to provide peer support
* Multipar
* Mothers with successful breastfeeding experience (Exclusive breastfeeding of the previous baby for at least 6 months, continued breastfeeding at the age of 2 years or older)
* At least secondary education graduate
* Singleton birth
* Vaginal birth (due to rapid mobilisation after birth and quicker adaptation to daily activities)
* with a child aged 5 years and under (limit for the age of the previous child for the memory factor regarding breastfeeding experience)
* Breastfeeding self-efficacy scale score of 60 and above (out of a total score of 70)
* No known or diagnosed psychiatric health problem in medical history
* Women without any health problem that may prevent breastfeeding will be included.
Intervention-Control group mothers
* Primipar
* 18 years and over
* Singleton birth
* No known or diagnosed psychiatric health problem in medical history
* Women who do not have any health problems that may prevent breastfeeding will be included.
Baby
* Born between 37-42 weeks
* Birth weight ≥2.5 kg and ≤3.9 kg
* 1 and 5 minute Apgar scores ≥8
* Not referred to neonatal intensive care unit
Exclusion criteria for individuals/patients in the study:
* Under 18 years of age
* Non-literate in Turkish
* Has a psychiatrically diagnosed health problem
* Developing a health problem that may prevent breastfeeding
* Taking medication that may jeopardise breastfeeding
* Women who do not want to participate will not be included in the study.
Exclusion criteria
* Requesting a room change
* Not wanting to/wanting to stop peer interaction within the scope of the room arrangement
* After settling in the room, those who did not want to answer the data collection tools for any reason/left the data collection tools unfinished
* Mothers who could not be reached in the postnatal 1st month follow-up will be excluded from the study.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
49 Years
Study:
NCT06277856
Study Brief:
Protocol Section:
NCT06277856