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 @ 10:10 PM
Ignite Modification Date:
2025-12-24 @ 10:10 PM
NCT ID:
NCT06646835
Eligibility Criteria:
Inclusion Criteria:
* Volunteering to participate in the research,
* Be over 18 years of age,
* Having a medically diagnosed risky condition during pregnancy (diabetes, hypertension, threat of preterm labor, pre-eclampsia, etc.),
* Compliance with at least one of the criteria in the "Ministry of Health Risk Assessment Form for Pregnancy" in the evaluation of current pregnancy,
* Planning a cesarean delivery,
* Being in the last trimester of pregnancy (28 weeks and above)
* Having a single live fetus,
* To be able to read and write Turkish.
Exclusion Criteria:
* A diagnosed psychiatric illness,
* Visual, hearing, speech, physical or mental disability,
* Any communication barriers,
* Cardiovascular disease in the pregnant woman and fetus,
* Fetal distress,
* Fetal anomaly,
* Any physical or medical condition that prevents the use of a stress ball,
* Need for urgent intervention before caesarean section according to the physician.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT06646835
Study Brief:
Protocol Section:
NCT06646835