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 @ 12:39 PM
Ignite Modification Date:
2025-12-24 @ 12:39 PM
NCT ID:
NCT05424861
Eligibility Criteria:
Inclusion Criteria:
* Having a single and live baby between 37-42 weeks of gestation,
* Normal spontaneous vaginal delivery,
* Multiparous,
* Having a baby weighing 2-4 kilograms,
* No general anesthetic agent was used at birth,
* Have not used a non-pharmacological method for pain before,
* Having a Visual Analogue Scale (VAS) score of 4 and above for uterine pain before breastfeeding,
* Not having breastfeeding problems,
* Not having any health problems (Tuberculosis, HIV, cancer, etc.),
* Having given birth at least 6 hours ago,
* Does not have any problems preventing communication,
* Able to read and write,
* Able to speak and understand Turkish,
* Volunteer mothers who agreed to participate in the study will be included.
Exclusion Criteria:
* Having a situation that prevents breastfeeding (galactosemia, congenital anomalies, etc.),
* Having postpartum complications (bleeding, infection, etc.),
* Separated from her baby for any reason after birth (in cases where the mother or baby is referred, hospitalized in intensive care or isolated),
* Having lost her baby,
* Having any complications during pregnancy (gestational diabetes, preeclampsia, Rh incompatibility, heart disease, etc.),
* With uterine anomaly,
* Tissue integrity deteriorated in the area to be treated,
* Taking painkillers in the last 6 hours,
* Smoking or using alcohol,
* Those with positive Covid-19 test will be excluded from the study. In addition, those who want to leave the research at any stage of the research will be excluded from the research.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
35 Years
Study:
NCT05424861
Study Brief:
Protocol Section:
NCT05424861