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 @ 4:25 AM
Ignite Modification Date:
2025-12-25 @ 4:25 AM
NCT ID:
NCT06085820
Eligibility Criteria:
Inclusion Criteria:
* Those who agree to participate in the research, are over 18 years old and speak Turkish,
* Primiparous pregnant women who do not have any physical or chronic disease and are in the latent phase,
* Pregnant women who do not have a risky pregnancy,
* 38-42. gestational age, singleton pregnant women,
* Absence of diagnosed fetal malformations,
* No medical problems at the beginning of the study,
* Amniotic membranes are not opened,
* Women who are at least primary school graduates will be included in the research.
Exclusion Criteria:
* Pregnant women who received epidural analgesia in the first stage of labor,
* Pregnant women whose labor lasts less than 3 hours will not be included in the study.
* In case of any complications or cesarean section, the sample will be removed from the study.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT06085820
Study Brief:
Protocol Section:
NCT06085820