Clinical Trial Details
— Status: Not yet recruiting
Administrative data
NCT number |
NCT06231602 |
Other study ID # |
202310157RINC |
Secondary ID |
|
Status |
Not yet recruiting |
Phase |
|
First received |
|
Last updated |
|
Start date |
February 1, 2024 |
Est. completion date |
December 31, 2024 |
Study information
Verified date |
November 2023 |
Source |
National Taiwan University Hospital |
Contact |
HUNG-HUI CHEN |
Phone |
011-886-2-2394-7109 |
Email |
hunghuichen[@]ntu.edu.tw |
Is FDA regulated |
No |
Health authority |
|
Study type |
Observational
|
Clinical Trial Summary
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).
Description:
Background: Perinatal depression and infant feeding (breastfeeding and complementary feeding)
are important global health issues. The prevalence of perinatal depression is high around the
world, and breastfeeding rates in middle- and high-income countries are on a downward trend.
Past research has pointed out that perinatal depression is related to infant feeding.
However, there is a lack of research on the impact of maternal depression on infant feeding
in Asian Chinese pregnant women, and "whether there is a bidirectional causal relationship
between postpartum depression and infant feeding" remains unclear.
Purpose: To explore the impact of pregnancy depression on infant feeding, and to explore the
two-way relationship between postpartum depression and infant feeding.
Method: This is a longitudinal cohort study. It's estimated to recruit 500 pregnant women. 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. This study will collect data by questionnaires distributed a total four times
(24 weeks of pregnancy to before delivery, 2 month postpartum, 4 month postpartum, 6 month
postpartum). Variables include: sociodemographics, maternal variables (parity, number of
births, planned pregnancy, maternal complications, mode of delivery, height and weight during
pregnancy and postpartum, blood pressure), infant variables (gender, health status , height,
weight), anticipatory feeding schedule, health-risk behaviors (smoking and alcohol use),
social support, situation of breastfeeding and complementary feeding, reactive feeding,
sleep, fatigue, exercise habits, and tendency to depression.