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 @ 3:14 PM
Ignite Modification Date:
2026-03-26 @ 3:14 PM
NCT ID:
NCT07323459
Eligibility Criteria:
Inclusion Criteria:
* Pregnant women in the second or third trimester of pregnancy
* Elevated level of pregnancy-related anxiety (PrA)
* Low obstetric risk pregnant women (no significant medical contraindications to vaginal delivery)
* Consent to participate in individual psychoeducational sessions
* Ability to communicate in Polish at a level sufficient to understand the materials and participate in the sessions
Exclusion Criteria:
* Pregnant women with severe mental disorders requiring urgent psychiatric intervention
* Women with serious obstetric complications in the current pregnancy requiring intensive medical monitoring (e.g., severe hypertension, imminent preterm delivery requiring hospitalization)
* Patients already undergoing intensive psychotherapy or pharmacotherapy for anxiety
* Lack of consent to participate or inability to attend sessions (e.g., due to logistical reasons)
* Pregnant women whose pregnancy-related anxiety is not the primary concern, with other dominant anxiety disorders (e.g., GAD unrelated to pregnancy) or other priority health needs
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT07323459
Study Brief:
Protocol Section:
NCT07323459