Salutogenesis theory on the postpartum quality of life
Not Applicable
- Conditions
- Postpartum quality of life.-
- Registration Number
- IRCT20230626058592N1
- Lead Sponsor
- Ahvaz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 110
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
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
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method 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.