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:
2026-03-26 @ 3:20 PM
Ignite Modification Date:
2026-03-26 @ 3:20 PM
NCT ID:
NCT07430020
Eligibility Criteria:
Inclusion Criteria:-Irani
* Primiparous pregnant women
* Gestational age between 35 and 37 weeks at enrollment
* Singleton pregnancy
* First breastfeeding experience
* Planned delivery in Zahedan hospitals
* Maternal age between 15 and 40 years
* Receiving care at comprehensive health centers in Zahedan, Iran
* Willingness to participate and provide informed consent
Exclusion Criteria:
* Contraindications to breastfeeding (e.g., chemotherapy, ergotamines, breast lesions, HIV infection, prenatal depression)
* Preterm birth (\<37 weeks)
* Neonatal intensive care unit (NICU) admission
* Absence from counseling sessions
* Congenital anomalies in the infant (e.g., cleft lip or palate)
* Maternal intensive care unit (ICU) admission
* High-risk pregnancy (e.g., pre-eclampsia/eclampsia, insulin-dependent diabetes, cardiac disease)
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
15 Years
Maximum Age:
45 Years
Study:
NCT07430020
Study Brief:
Protocol Section:
NCT07430020