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 @ 10:04 PM
Ignite Modification Date:
2025-12-24 @ 10:04 PM
NCT ID:
NCT06155435
Eligibility Criteria:
Inclusion Criteria:
* Agreeing to participate in the research
* Being over 20 years old
* Being able to speak Turkish
* Not having any disability such as hearing or vision
* Being nulliparous pregnant
* Being in the 3rd trimester (those who are pregnant between 28-35 weeks)
* Not having received any psychiatric diagnosis before
* No risk of vaginal bleeding, hypertension, diabetes, multiple pregnancy etc. during pregnancy.
* Not having any physical/mental problems that would prevent normal birth.
Exclusion Criteria:
* Pregnant women in high risk groups (arthritis, premature birth, placenta previa, etc.)
* Multigravida pregnant women (pregnant women with 2 or more pregnancies)
* Having received any psychiatric diagnosis and/or receiving psychiatric treatment.
The termination criteria for the cases included in the study will be as follows:
* Intrauterine fetal death during pregnancy,
* Emergence of any risk during pregnancy,
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
20 Years
Maximum Age:
39 Years
Study:
NCT06155435
Study Brief:
Protocol Section:
NCT06155435