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 @ 4:16 PM
Ignite Modification Date:
2025-12-24 @ 4:16 PM
NCT ID:
NCT06179966
Eligibility Criteria:
Inclusion Criteria:
* knowing Turkish
* Being over 18 years old
* Having a second vaginal birth
* Being able to go through the labor process with his/her spouse
* Dilation ≤5cm during vaginal examination during admission to labor
* Pregnancy period is between 36-40 weeks
* Agreeing to participate in the research with a voluntary consent form
* Do not use any non-pharmacological method before admission to labor. not to have used
* Not using any analgesic or anesthetic medication during labor.
Exclusion Criteria:
* Having any chronic disease (DM, HT, Heart Disease)
* Receiving psychiatric treatment (Pharmacotherapy and/or Psychotherapy)
* Presence of a risky pregnancy that prevents normal birth (oligohydramnios, polyhydramnios, twin pregnancy, placental anomalies, presentation and position anomalies)
* Presence of a wound that disrupts skin integrity
* Having given birth 3 or more times
* Being the first pregnancy
* Exceeding term (\>40 weeks) or premature birth (\<36 weeks)
* Presence of previous uterine surgery (caesarean section indication)
* Not having a partner during labor
* Have the necessary examination findings to be accepted into the specified research.
not having
* The birth process ends with a cesarean section
* Having an operative birth (vacuum, forceps)
* Wants to leave the research voluntarily.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
20 Years
Maximum Age:
35 Years
Study:
NCT06179966
Study Brief:
Protocol Section:
NCT06179966