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A Study on the Influencing Factors of Fertility Willingness among Women of Childbearing Age and Their Relationship with Antenatal Depression

A Study on the Influencing Factors of Fertility Willingness among Women of Childbearing Age and Their Relationship with Antenatal Depression

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121174
Enrollment
Unknown
Registered
2026-03-26
Start date
2026-03-26
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Perinatal depression

Interventions

Observation group:None

Sponsors

Zhujiang Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 49 Years

Inclusion criteria

Inclusion criteria: 1. Women of childbearing age between 20 and 49 years old who are currently in the preconception period (i.e., have a plan to have children within the next 1-2 years, or have initiated preconception health care, lifestyle adjustments, or other preconception preparation behaviors); 2. Voluntarily participate in this study, fully understand the research purpose, procedures, and potential risks, and sign a written informed consent form; 3. Have normal language communication and comprehension abilities, no communication barriers (such as hearing impairment, language expression, etc.), and can complete questionnaire filling and follow-up at various time points independently or with assistance; 4. Commit to cooperating with the longitudinal follow-up process of this study: "preconception period (T1) early pregnancy (T2, before 13+6 weeks of gestation) second trimester (T3, 14-27+6 weeks of gestation) third trimester (T4, 28 weeks of gestation and later) postpartum (T5, within 6 weeks after delivery)".

Exclusion criteria

Exclusion criteria: 1. Women who have confirmed pregnancy (are in the pregnancy period) or are within 6 months postpartum (excluding the group not in the pregnancy-preparation period to ensure the research subjects focus on those in the pregnancy-preparation period); 2. Women with severe physical diseases (such as malignant tumors, severe cardiovascular and cerebrovascular diseases, chronic renal failure, etc.) or who are unable to cooperate in completing questionnaires and follow-ups due to their physical conditions; 3. Women who explicitly refuse to cooperate with the longitudinal follow-up of this study (such as refusing secondary data collection in the first and second trimesters) (longitudinal studies require a complete data chain, excluding those with insufficient willingness to follow up); 4. Women with a history of mental illness (such as depression, anxiety, schizophrenia, etc.) or currently having psychotic disorders (diagnosed by clinical diagnosis or self-report) (to avoid interference from past/current mental illnesses on the assessment of "prenatal depression").

Design outcomes

Primary

MeasureTime frame
depression;

Countries

China

Contacts

Public ContactXiuyun Cao

Zhujiang Hospital of Southern Medical University

cxyzml@163.com+86 20 6278 3230

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 4, 2026