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:
2025-12-25 @ 3:04 AM
Ignite Modification Date:
2025-12-25 @ 3:04 AM
NCT ID:
NCT06250933
Eligibility Criteria:
Inclusion Criteria:
* Willing to participate in the study
* Without communication barriers
* Literate
* Married
* Not undergoing psychological treatment
* Preterm birth occurring between gestational weeks 28-32
* Mothers of preterm infants receiving continuous treatment in the NICU (Neonatal Intensive Care Unit) at the time of data collection
* Not having received breastfeeding education from healthcare professionals
Exclusion Criteria:
* The baby dies during the treatment process
* Not participating in the stages of the research
* Asking to withdraw from the study
Healthy Volunteers:
True
Sex:
FEMALE
Study:
NCT06250933
Study Brief:
Protocol Section:
NCT06250933