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 @ 3:30 AM
Ignite Modification Date:
2025-12-25 @ 3:30 AM
NCT ID:
NCT07238205
Eligibility Criteria:
Inclusion Criteria:
* Enrolled in the Midwifery Department at Mardin Artuklu University,
* Taking the course "Normal Birth and Postpartum Care,"
* Who have not previously received any structured training (practical training, simulation, etc.) related to vaginal examination or cervical dilation/effacement procedures,
* Who do not feel confident in assessing cervical effacement and dilation,
* Who volunteer to participate in the study will be included,
* Pregnant women who are in the first stage of labor and have no obstetric complications.
Exclusion Criteria:
* Individuals who are graduates of health vocational high schools,
* Have disabilities in their eyes, hands, arms, or fingers,
* Those who do not complete the training will not be included.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Months
Maximum Age:
35 Years
Study:
NCT07238205
Study Brief:
Protocol Section:
NCT07238205