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Construction and effect evaluation of a classified intervention program for prenatal depression in pregnant women based on different types of rumination

Construction and effect evaluation of a classified intervention program for prenatal depression in pregnant women based on different types of rumination

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112669
Enrollment
Unknown
Registered
2025-11-18
Start date
2025-11-24
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

Prenatal depression: including prenatal depressive disorder (requiring diagnosis by a psychiatrist) and prenatal depressive symptoms (measured by a scale). This study focuses on the latter, referring to a series of negative emotional states in pregnant women, primarily characterized by feelings of sadness and diminished interest in activities. It is assessed using the Edinburgh Postnatal Depressio

Interventions

Adaptive group:Mindfulness Therapy
Non-rumination group:expressive writing
Maladaptive group:Acceptance and Commitment Therapy

Sponsors

Southern Medical University Southern Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 20 years old; 2. Natural conception, single live birth, second trimester of pregnancy; 3.Educational level above primary school, clear thinking, normal expression; 4. EPDS score >= 9; 5. Informed consent, signed informed consent form, voluntary participation in the study.

Exclusion criteria

Exclusion criteria: 1. Having a mental illness or history of mental illness (such as depression, anxiety, etc.); 2.Suffering from severe major physical diseases of the heart, brain, etc. (such as myocardial infarction, cerebral infarction, etc.); 3. Having taken antipsychotic drugs or other drugs that may affect mental state within the past 6 months; 4. Being under psychological counseling or participating in other research.

Design outcomes

Primary

MeasureTime frame
prenatal depression;

Secondary

MeasureTime frame
Satisfaction With Life;

Countries

China

Contacts

Public ContactHuang Yingying

Southern Medical University Southern Hospital

gyq170909@126.com+86 20 62787291

Outcome results

None listed

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