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 @ 10:21 PM
Ignite Modification Date:
2025-12-24 @ 10:21 PM
NCT ID:
NCT07031635
Eligibility Criteria:
Inclusion Criteria:
* Primiparous women who were expected to give birth vaginally
* Women who became pregnant spontaneously
* Women who were in the latent phase of labor upon admission
* Women who were not given oxytocin
* Women who were at term (38-42 weeks of gestation)
* Women who had a single healthy fetus in the vertex position
* Women who did not have any risk factors (such as preeclampsia, eclampsia, placenta previa, or placental abruption).
Exclusion Criteria:
* Pregnant women with any complications that could cause dystocia during labor (such as contraction abnormalities birth objects, birth canal dystocia, maternal psychological dystocia)
* Who are unable to move
* Who cannot speak, read, or understand Turkish
* Who have communication problems.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
49 Years
Study:
NCT07031635
Study Brief:
Protocol Section:
NCT07031635