Postpartum quality of life. -
Conditions
Interventions
Intervention 1: Intervention group: The educational content is prepared based on the determinants effective in improving the quality of life after childbirth in primiparous women, which will be obtain
Sponsors
Ahvaz University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Nulliparous women Being at gestational age 28 weeks and above Being over 18 years old Singleton pregnancy Ultrasound confirmation of fetus health Having no history of depression or long-term medical illness in the past according to the mother's statement Willingness to participation the study
Exclusion criteria
Exclusion criteria: Women with a history of infertility Pregnancy following assisted reproductive treatment. Refusing to complete questionnaires Cannot be accessed for unpredictable reasons. The presence of illness in the spouse
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postpartum quality of life. Timepoint: Immediately after delivery, 4 weeks after delivery and 8 weeks after delivery. Method of measurement: Using the postpartum quality of life questionnaire.;Type of delivery. Timepoint: After delivery. Method of measurement: Examination of maternity records. | — |
Secondary
| Measure | Time frame |
|---|---|
| Sense of coherence. Timepoint: Before the intervention, immediately after delivery, 4 weeks after delivery and 8 weeks after delivery. Method of measurement: SOC-13 questionnaire.;Maternal self-efficacy. Timepoint: Immediately after delivery, 4 weeks after delivery and 8 weeks after delivery. Method of measurement: Maternal self-efficacy questionnaire.;Breastfeeding self-efficacy. Timepoint: Immediately after delivery, 4 weeks after delivery and 8 weeks after delivery. Method of measurement: Breastfeeding Self-Efficacy Scale-Short Form. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMaryam Shami
Ahvaz University of Medical Sciences
Outcome results
None listed