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 @ 4:30 AM
Ignite Modification Date:
2025-12-25 @ 4:30 AM
NCT ID:
NCT05584618
Eligibility Criteria:
Inclusion Criteria:
* Literate
* Childbirth at fullterm (born at 38-42 weeks)
* Nulliparous women
* Women between the ages of 18-35
* Singleton pregnancy in 20 and 36 weeks of gestation
* Having a healthy newborn
* No participation in another prenatal program
* Absence of any psychiatric illness or comorbidities
* No use medications for a diagnosed mental disorder
* Baby with normal birth weight and APGAR score of 8 and above
* Women who have not developed postpartum complications
* Women without complicated/high-risk pregnancies, who do not experience a perinatal death or stillbirth
* Speaks and understands Turkish
* Women with a total fear of childbirth score W-DEQ-A ≥60 will be included.
* Women who give birth through vaginal route
Exclusion Criteria:
• Women who do not meet the sample selection criteria
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
35 Years
Study:
NCT05584618
Study Brief:
Protocol Section:
NCT05584618