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The application of dyadic coping in reducing pregnancy complications

The application of dyadic coping in reducing pregnancy complications

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600122606
Enrollment
Unknown
Registered
2026-04-15
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-04-20

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

Conditions

pregnancy complications

Interventions

High-level dyadic coping group:None
Normal dyadic coping group:None
Low-level dyadic coping group:None

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Natural pregnancy; 2. Age > 18 years old; 3. Complete reading, comprehension and language abilities, clear consciousness and the ability to make independent judgments; 4. Color Doppler ultrasound indicates no abnormalities in the fetus; 5. Voluntarily participate in this study; 6. Live with a spous.

Exclusion criteria

Exclusion criteria: 1. Unnatural pregnancy; 2. Severe complications, such as moderate preeclampsia and heart disease during pregnancy; 3. Have a mental illness; 4. Those who are unaware of their illness.

Design outcomes

Primary

MeasureTime frame
Dyadic Supportive Coping Scale score;

Secondary

MeasureTime frame
depressive state;postpartum complications;

Countries

China

Contacts

Public ContactBingxin Wang

Shanghai General Hospital

004642wbx@shgh.cn+86 21 37798630

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 23, 2026