education: pregnant women will be given a 4-week training and the pre-test post-test will be analyzed
Study summary
During pregnancy, women are exposed to physical, psychological and social changes and may experience anxiety and fears about childbirth. Traumatic birth perception is defined as perceiving birth as a threat to oneself and one\'s baby. This perception can negatively affect women\'s lives in the postpartum period. Midwives are the primary health professionals in preventing traumatic birth perception. In this context, it is envisaged to create an important basis for preventing traumatic birth perception in pregnant women through the training to be given.
Eligibility
Sex
FEMALE
Min age
18 Years
Max age
40 Years
Healthy volunteers
Accepted
Inclusion Criteria: - Volunteering to participate in the study,
* 18 years of age or older,
* At least 53 points from the Traumatic Birth Perception Scale
* No pregnancy-related risks (such as pre-eclampsia, diabetes, heart disease, placenta previa, oligohydramnios),
* The fetus has no health problems (fetal anomaly, intrauterine growth retardation, etc.),
* Literate,
Exclusion Criteria: - Refused to participate in the research,
* Illiterate,
* Has a disorder based on a psychiatric/psychological diagnosis,
* Pregnant women with communication and language problems will not be included in the study.
Primary outcome measure(s)
pre-test post-test — 1 month The traumatic Childbirth Perception scale in pregnant women will be used as a pre-test and post-test. The experimental and control groups of the study will consist of pregnant women who scored at least 53 points on the Traumatic Childbirth Perception Scale. The minimum traumatic birth perception scale score is 0, and the maximum is 130. Scale total score 0-26 points range is very low, 27-52 points range is low, 53-78 points range is medium, 79-104 points range is high, and 105-130 points range is very high traumatic birth perception level.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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