Condition 1: childbirth preparation. Condition 2: fear of childbirth.
Conditions
Interventions
Intervention 1: Intervention group: The designed web application will be installed on the smartphones of participants in the intervention group. Its content will be personalized so that, at the beginn
Sponsors
Tabriz University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
15 Years to 49 Years
Inclusion criteria
Inclusion criteria: Gestational age of 24 to 32 weeks Singleton pregnancy Literacy (ability to read and write) Ability to use a mobile application Not having a medical field education Possession of a smartphone
Exclusion criteria
Exclusion criteria: Development of any pregnancy complications, such as preeclampsia. Bleeding and intrauterine fetal death. Multiple pregnancy Presence of chronic diseases or conditions that are induced or exacerbated by pregnancy, such as hypertension, cardiovascular diseases, diabetes, preeclampsia, etc. Indications for cesarean section, such as placenta previa, non-cephalic presentations, abnormal fetal heart rate patterns, etc. History of cesarean section or uterine surgery/scarring. Previous participation in physiological childbirth classes. Abnormal pregnancy conditions, such as polyhydramnios, oligohydramnios, or intrauterine growth restriction (IUGR).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Childbirth preparation score. Timepoint: Before the intervention and 4 weeks after the intervention. Method of measurement: Childbirth Readiness Scale(CRS).;Fear of childbirth score. Timepoint: Before the intervention and 4 weeks after the intervention and 24 hours after delivery. Method of measurement: Wijma delivery expectancy/experience questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Childbirth experience score. Timepoint: 24hours after delivery. Method of measurement: Childbirth Experiences (CEQ-2.0) 2.0 Questionnaire version.;Child Birth Self Efficacy score. Timepoint: Before the intervention and 24 hours after delivery. Method of measurement: Child Birth Self Efficacy questionnaire.;Postpartum depression literacy score. Timepoint: Before the intervention and 4 weeks after the intervent. Method of measurement: Postpartum depression literacy Scale (PoDLiS).;Frequency of mode of delivery. Timepoint: 24 hours after delivery. Method of measurement: Frequency of mode of delivery check list. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr.Esmat Mehrabi
Tabriz University of Medical Sciences
Outcome results
None listed