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Postpartum Anxiety, Breastfeeding and Infant Health Among Taiwanese Women

Effects of Postpartum Anxiety on Breastfeeding and Infant Health Among Taiwanese Women: a Longitudinal Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04608721
Enrollment
315
Registered
2020-10-29
Start date
2020-11-04
Completion date
2023-01-10
Last updated
2022-07-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breastfeeding, Infant Conditions, Postpartum Anxiety

Brief summary

This is a prospective, longitudinal and observational study designed to investigate the trajectories of postpartum anxiety and its determinants in the first year after childbirth. This study also examine the associations between postpartum anxiety and infant health outcome, including breastfeeding patterns, excessive crying and body weight growth. Primipara aged 20-49 with term baby will be invited. Demographics, maternal-newborn characteristics, and anxiety symptoms will be collected during the first week postpartum (T1). Questionnaires will be follow-up by mail and telephone reminder in 1 (T2), 3 (T3), 6 (T4) and 12 months (T5) postpartum. The primary outcome is postpartum anxiety using the Spielberger's State-Trait Anxiety Inventory (STAI); the secondary outcomes are infant health outcomes including breastfeeding patterns, excessive crying and body weight growth. A linear mixed model (LMM) is used to determine the trajectories of postpartum anxiety over time and to examine whether specific demographic and maternal characteristics predict the trajectories of postpartum anxiety. The key findings may contribute to promote early identification and secondary preventive interventions for women with postpartum anxiety.

Detailed description

Ditto

Interventions

OTHERPostpartum Anxiety

Postpartum anxiety will be assessed at 1-3 days (T1), 1(T2), 3 (T3), 6 (T4) and 12 months (T5) postpartum by using the State-Trait Anxiety Inventory (STAI) with a score ≥40 serving as a positive screen.

Sponsors

Fu Jen Catholic University
CollaboratorOTHER
Ministry of Science and Technology, Taiwan
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 49 Years
Healthy volunteers
Yes

Inclusion criteria

* 20-49 years old * Primipara

Exclusion criteria

* Preterm birth * Infants with severe congenital malformations/medical conditions or Fetal/neonatal death * Current use of antidepressant or antipsychotics * Thoughts of self-harm or suicide

Design outcomes

Primary

MeasureTime frameDescription
Postpartum anxietyBaselineAssessments using the Spielberger's State-Trait Anxiety Inventory (STAI) for self-reported anxiety symptoms

Secondary

MeasureTime frameDescription
Infant health outcomesBaselineIncluding breastfeeding patterns, excessive crying and body weight growth

Countries

Taiwan

Contacts

Primary ContactYuh-Kae Shyu
094528@mail.fju.edu.tw886-2-29053500

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026