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 @ 3:20 AM
Ignite Modification Date:
2025-12-25 @ 3:20 AM
NCT ID:
NCT07165405
Eligibility Criteria:
Inclusion Criteria:
* Volunteering to participate in the study
* Expectation of spontaneous vaginal delivery
* Estimated fetal weight between 2500-4000 grams by ultrasound
* Single fetus and cephalic presentation,
* Term pregnancy (between 37-42 weeks of gestation)
* Being in the active phase of labor (cervical dilation of 4 cm)
* No analgesia or anesthesia used during the first stage of labor,
* No skin disease or open wound preventing massage or showering
Exclusion Criteria:
* Having undergone infertility treatment,
* Delivery by cesarean section for any reason during labor,
* Being multiparous
* Having any systemic, chronic, or neurological disease (Diabetes Mellitus, Hypertension, Thyroid disorders, Multiple Sclerosis, Epilepsy, etc.)
* Regular medication use due to any illness,
* Active psychiatric treatment (pharmacotherapy/psychotherapy),
* Any induction that may affect uterine contractions and dilation,
* Any pregnancy complications (such as placenta previa, preeclampsia, premature rupture of membranes, oligohydramnios, and polyhydramnios)
* Interventional delivery (forceps, vacuum)
* Any problem that hinders communication (such as not knowing Turkish, hearing, speech, and comprehension disorders)
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT07165405
Study Brief:
Protocol Section:
NCT07165405