The Relationship Between Maternal Perinatal Depression and Feeding Behavior Among Primiparas

November 16, 2025 updated by: National Taiwan University Hospital
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).

Study Overview

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

Observational

Enrollment (Estimated)

500

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Taipei, Taiwan
        • Recruiting
        • National Taiwan University Hospital
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study 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.

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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
Depression was measured using the Edinburgh Postnatal Depression Scale.
24 weeks of pregnancy to before delivery, 2 month postpartum, 4 month postpartum, 6 month postpartum
breastfeeding situation
Time Frame: 2 month postpartum, 4 month postpartum, 6 month postpartum
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.
2 month postpartum, 4 month postpartum, 6 month postpartum
complementary feeding situation
Time Frame: 4 month postpartum, 6 month postpartum
Questions contain types of food, starting age of introduction, daily feeding amount and daily feeding times, etc.
4 month postpartum, 6 month postpartum
maternal variables
Time Frame: 24 weeks of pregnancy to before delivery, 2 month postpartum, 4 month postpartum, 6 month postpartum
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).
24 weeks of pregnancy to before delivery, 2 month postpartum, 4 month postpartum, 6 month postpartum
infant variables
Time Frame: 2 month postpartum, 4 month postpartum, 6 month postpartum
Questions contain gender, health status , height in centimeters, weight in grams.
2 month postpartum, 4 month postpartum, 6 month postpartum

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: HUNG-HUI CHEN, National Taiwan University Hostiptal

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 19, 2024

Primary Completion (Estimated)

December 31, 2026

Study Completion (Estimated)

December 31, 2026

Study Registration Dates

First Submitted

January 21, 2024

First Submitted That Met QC Criteria

January 21, 2024

First Posted (Actual)

January 30, 2024

Study Record Updates

Last Update Posted (Actual)

November 19, 2025

Last Update Submitted That Met QC Criteria

November 16, 2025

Last Verified

November 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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