The Effect of the Continuous Midwifery Care Model on Birth Outcomes
Birth, First, Pregnancy Related, Newborn; Fit
About this trial
This is an interventional supportive care trial for Birth, First focused on measuring birth, midwifery care model, birth trauma, post traumatic stress disorder, pregnancy education
Eligibility Criteria
Inclusion Criteria: Pregnant women who have completed at least primary education, Able to speak, understand and write Turkish, Pregnant women between the ages of 18-35 (pregnant women under 18 and over 35 years of age will not be preferred since they are among the risky groups in terms of maternal and fetal) Pregnant women residing within the borders of Mersin-Tarsus Primigravidas (It is planned to include primigravidas in the study, considering that there may be different variables affecting the fear of childbirth in previous pregnancies of multiparas.) Pregnant women who do not have any obstacles to give vaginal birth Pregnant women with a single and healthy fetus will be included in the study. Exclusion Criteria: Pregnant women with any risky pregnancy history (preeclampsia, placenta previa, gestational diabetes mellitus, oligohydramnios and polyhydramnios, etc.), Pregnant women with systemic and/or neurological disease, Pregnant women with cesarean indication, Pregnant women with chronic and/or psychiatric health problems (based on self-report and clinical diagnosis), Pregnant women who participated in any childbirth preparation training program
Sites / Locations
- Tarsus UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Randomization group
Control group
Pregnant women in the study group will be given a total of 4 modules, 3 modules during pregnancy and 1 module in the postpartum period; 1. module 20-28. During pregnancy weeks, trainings are in the form of face-to-face group training, 2. module 29-36. During pregnancy weeks, trainings are in the form of face-to-face group training, 3. module trainings 37-40. in the form of video-conference (zoom meeting) during pregnancy weeks, 4. module will be applied in 1 month postpartum with face-to-face interview technique). Pregnancy 20-28. Pregnant women between weeks 29-36 should attend the 1st module education. 2nd module training in gestational weeks, 37-40. They will be trained in the 3rd module during the pregnancy weeks. module training will be individualized during the mother's visit in the 1st month postpartum. Version B (WDEQ) will be administered after the program is completed, and the Birth-Related Trauma Perception Scale will be administered after birth.
Pregnant women who will be included in the control group will receive routine midwifery care. In the postpartum period (WDEQ), version B and the Birth Trauma Perception Scale will be used. The pregnant women will inform the researcher by telephone after the birth (within the first 24 hours) and the mother will be visited by the researcher within the first month after the birth, and the trauma perceptions of the mothers will be evaluated with the Birth Trauma Perception Scale.