- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06231602
The Relationship Between Maternal Perinatal Depression and Feeding Behavior Among Primiparas
Study Overview
Status
Detailed 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.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: HUNG-HUI CHEN
- Phone Number: 886-2-2394-7109
- Email: hunghuichen@ntu.edu.tw
Study Locations
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Taipei, Taiwan
- Recruiting
- National Taiwan University Hospital
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Contact:
- HUNG-HUI CHEN
- Phone Number: +886-2-23947109
- Email: hunghuichen@ntu.edu.tw
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- 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
Exclusion Criteria:
- No exclusion conditions
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
perinatal depression
Time Frame: 24 weeks of pregnancy to before delivery, 2 month postpartum, 4 month postpartum, 6 month postpartum
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Depression was measured using the Edinburgh Postnatal Depression Scale.
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24 weeks of pregnancy to before delivery, 2 month postpartum, 4 month postpartum, 6 month postpartum
|
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breastfeeding situation
Time Frame: 2 month postpartum, 4 month postpartum, 6 month postpartum
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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.
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2 month postpartum, 4 month postpartum, 6 month postpartum
|
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complementary feeding situation
Time Frame: 4 month postpartum, 6 month postpartum
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Questions contain types of food, starting age of introduction, daily feeding amount and daily feeding times, etc.
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4 month postpartum, 6 month postpartum
|
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maternal variables
Time Frame: 24 weeks of pregnancy to before delivery, 2 month postpartum, 4 month postpartum, 6 month postpartum
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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).
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24 weeks of pregnancy to before delivery, 2 month postpartum, 4 month postpartum, 6 month postpartum
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infant variables
Time Frame: 2 month postpartum, 4 month postpartum, 6 month postpartum
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Questions contain gender, health status , height in centimeters, weight in grams.
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2 month postpartum, 4 month postpartum, 6 month postpartum
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Collaborators and Investigators
Investigators
- Principal Investigator: HUNG-HUI CHEN, National Taiwan University Hostiptal
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 202310157RINC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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