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 @ 3:13 AM
Ignite Modification Date:
2025-12-25 @ 3:13 AM
NCT ID:
NCT05033405
Eligibility Criteria:
Inclusion Criteria:
* The study included individuals who
* had a cesarean section,
* were at the 6th to 24th hour postpartum,
* agreed to participate in the study,
* had a cesarean section for the first time,
* did not use patient-controlled analgesia (PCA),
* did not have an additional health problem that may cause pain in the postpartum period, other than cesarean incision pain, and
* could speak and understand Turkish.
Exclusion Criteria:
* Mothers who wanted to quit on their own will at any stage after being included in the study, had verbal communication problems, had hearing or vision problems, or had previously been diagnosed with a psychiatric illness were excluded from the sample.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
19 Years
Maximum Age:
42 Years
Study:
NCT05033405
Study Brief:
Protocol Section:
NCT05033405