Women's Perception of Respectful Maternity Care, Birth Experiences and Perception of Traumatic Birth
- Conditions
- MaternityBirth, FirstTraumatic BirthIntrapartum Fetal Distress
- Registration Number
- NCT06691854
- Lead Sponsor
- Selcuk University
- Brief Summary
The effect of the ıntrapartum care model given in line with the world health organization (WHO) recommendations on women's perception of respectful maternity care, birth experiences and perception of traumatic birth
- Detailed Description
The research is a randomized controlled trial. The research will conducted with 124 primiparous pregnant women (intervention group n=62, control group n=62) who were hospitalized in the delivery unit of Aksaray Training and Research Hospital between September 2023 and January 2024. The pregnant women in the intervention group will given the intrapartum care model in line with WHO recommendations after cervical dilation reached 5 cm. The control group will received only the standard intrapartum care in the hospital. Data will be collected using the personal information form, birth follow-up form, respectful maternal care scale, birth experience scale, and traumatic birth perception scale.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- Female
- Target Recruitment
- 124
- Those who are 18 years of age or older,
- Those who are in term pregnancy (38-41 weeks),
- Those who are primiparous,
- Those who have a single, healthy, vertex positioned fetus,
- Those who have cervical dilatation of 5 cm or more,
- Those who can speak and understand Turkish,
- Those who voluntarily agree to participate in the research.
- Those with chronic diseases (hypertension, diabetes, etc.),
- Those with a diagnosed mental illness (depression, anxiety or other psychotic disorder, etc.),
- Those with maternal and fetal complications (oligohydramnios and polyhydramnios, placenta previa, preeclampsia, premature membrane rupture, presentation anomalies, intrauterine growth retardation, fetal anomalies, intrauterine death, macrosomic baby, cord prolapse, etc.),
- Those with any complications that prevent vaginal birth (cephalopelvic disproportion, etc.),
- Elective cesarean section,
- Those who became pregnant with assisted reproductive techniques,
- Those who received childbirth preparation training.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Comparison of sociodemographic characteristics of pregnant women before the intervention with the questionnaire 6 months Sociodemographic of pregnant women will be collected through surveys and compared and reported
Comparison of pre-intervention obstetric characteristics of pregnant women with a questionnaire 6 months Obstetric of pregnant women will be collected through surveys and compared and reported
Comparison of the delivery times of pregnant women through a survey 6 months The duration of labor of the groups will be collected through surveys and compared and reported
Comparison of the means of the respectful birth care scale among pregnant women by group 6 months The respectful maternity care scale will be applied to pregnant women. The respectful maternity care scale is 19-95 points (min-max), and as the score increases, women's respectful maternity care increases.
Comparison of the means of the birth experience scale among pregnant women by group 6 months The birth experience scale will be applied to pregnant women. The birth experience scale is 22-88 points (min-max), and as the score increases, it indicates that the expectant mother has a good birth experience.
Comparison of the means of the traumatic birth perception scale among pregnant women by group 6 months The traumatic birth perception scale will be applied to pregnant women. The traumatic birth perception scale is 0-130 points (min-max). The scale shows that the 0-26 point range is "very low", the 27-52 point range is "low", the 53-78 point range is "medium", the 79-104 point range is "high", and the 105-130 point range is "very high" traumatic birth perception level.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Seyhan Çankaya
🇹🇷Konya, Turkey