Clinical Trial

The Effect of Continuous Midwife Support on Various Parameters Related to Pregnancy, Childbirth and Postpartum Period

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Record status
This record was last updated April 4, 2023 (before its estimated April 15, 2025 completion). Its status may not reflect the trial's current state.
Summary
There is a need for studies with a high level of evidence regarding the effect of supportive care given during the preconceptional period, pregnancy, childbirth and postpartum processes. With this planned study, it is aimed to evaluate the effect of continuous midwife support during pregnancy, birth and postpartum periods, starting from the preconceptional period, on various parameters related to pregnancy, birth and postpartum period. The research is planned as a randomized controlled experimental study. It consists of two groups, the study group and the control group. 75 women out of 150 women will form the control group and 75 women will form the study group. The women in the working group will be given individual training in line with their needs. Data will be collected by using the checklist and many scales used by the control and study groups in preconceptional counseling recommended by ACOG (American College of Obstetricians and Gynecologists).
Trial Details
NCT Number NCT05797363
Lead Sponsor Amasya University
Conditions Pregnant Women, Childbirth, Women's Health
Enrollment 150 participants
Start Date 2023-04-15
Primary Completion 2025-04-15 (estimated)
Study Completion 2027-12-30 (estimated)
Updated on ClinicalTrials.gov 2023-04-04