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 @ 2:15 AM
Ignite Modification Date:
2025-12-25 @ 2:15 AM
NCT ID:
NCT01601860
Eligibility Criteria:
Inclusion Criteria:
* Agreement of the patient to participate in the study after reading and signing the consent form;
* primigravida;
* Pregnancy unique;
* Gestational age\> 37 weeks;
* fetal cephalic presentation;
* chorioamniotic intact membranes;
* spontaneous labor;
* Admission to the beginning of the active phase of dilatation (4 cm cervical dilatation);
* Dynamics between 2 and 4 uterine contractions in ten minutes;
* Lack of maternal and fetal pathologies;
* literate;
* Absence of cognitive problems.
Exclusion Criteria:
Intolerance to non-pharmacological application of resources;
* Increased pain by the woman that prevents the completion of the intervention;
* Want to stop the intervention;
* Suspected acute suffering;
* Indication of cesarean section.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
15 Years
Maximum Age:
30 Years
Study:
NCT01601860
Study Brief:
Protocol Section:
NCT01601860