About this trial
The goal of this observational study is to explore the impact of pregnancy depression on infant feeding, and to explore the two-way relationship between postpartum depression and infant feeding. Participants will be asked to finish questionnaires four times (24 weeks of pregnancy to before delivery, 2 month postpartum, 4 month postpartum, 6 month postpartum).
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Primipara
Adult women over 18 years old
Those with no recurrent pregnancy loss and stable signs of pregnancy
Those who agree to participate in this study
Disqualifiers
No exclusion conditions
Trial population
It is planned to recruit participants at the Obstetrics and Gynecology Clinic of National Taiwan University Hospital. At the same time, research recruitment advertisements will also be posted online.
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
maternal variables
Questions contain parity, number of births, planned pregnancy, maternal complications, mode of delivery, height in centimeters, weight in kilograms, blood pressure, etc. Height and weight will be measured during pregnancy and postpartum(Height and weight will be combined to report BMI in kg/m\^2).
infant variables
Questions contain gender, health status , height in centimeters, weight in grams.
perinatal depression
Depression was measured using the Edinburgh Postnatal Depression Scale.
breastfeeding situation
Questions contain whether breastfeeding is continued, the type of feeding (breastfeeding or formula feeding), whether additional liquids are fed and the amount of feeding, etc.
Sponsors and contacts
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