NCT06231602

Brief 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).

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
500

participants targeted

Target at P75+ for all trials

Timeline
8mo left

Started Feb 2024

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress77%
Feb 2024Dec 2026

First Submitted

Initial submission to the registry

January 21, 2024

Completed
9 days until next milestone

First Posted

Study publicly available on registry

January 30, 2024

Completed
20 days until next milestone

Study Start

First participant enrolled

February 19, 2024

Completed
2.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Last Updated

November 19, 2025

Status Verified

November 1, 2025

Enrollment Period

2.9 years

First QC Date

January 21, 2024

Last Update Submit

November 16, 2025

Conditions

Keywords

prenatal depressionpostpartum depressionbreastfeedingcomplementary feeding

Outcome Measures

Primary Outcomes (5)

  • 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).

    24 weeks of pregnancy to before delivery, 2 month postpartum, 4 month postpartum, 6 month postpartum

  • infant variables

    Questions contain gender, health status , height in centimeters, weight in grams.

    2 month postpartum, 4 month postpartum, 6 month postpartum

  • perinatal depression

    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

    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

    Questions contain types of food, starting age of introduction, daily feeding amount and daily feeding times, etc.

    4 month postpartum, 6 month postpartum

Eligibility Criteria

Age18 Years+
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsThe participants of this study are pregnant women because this study aims to explore the impact of pregnancy depression on infant feeding, and to explore the two-way relationship between postpartum depression and infant feeding.
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-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.

You may qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Taiwan University Hospital

Taipei, Taiwan

RECRUITING

MeSH Terms

Conditions

Breast FeedingDepression, Postpartum

Condition Hierarchy (Ancestors)

Feeding BehaviorBehaviorPuerperal DisordersPregnancy ComplicationsFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesDepressive DisorderMood DisordersMental Disorders

Study Officials

  • HUNG-HUI CHEN

    National Taiwan University Hostiptal

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 21, 2024

First Posted

January 30, 2024

Study Start

February 19, 2024

Primary Completion (Estimated)

December 31, 2026

Study Completion (Estimated)

December 31, 2026

Last Updated

November 19, 2025

Record last verified: 2025-11

Data Sharing

IPD Sharing
Will not share

Locations