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Actor and partner effects of dyadic coping on maternal postpartum depressive symptoms after cesarean delivery: a prospective longitudinal dyadic study

Actor and partner effects of dyadic coping on maternal postpartum depressive symptoms after cesarean delivery: a prospective longitudinal dyadic study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600122922
Enrollment
Unknown
Registered
2026-04-20
Start date
2026-04-20
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

cesarean delivery

Interventions

cesarean women group:none
Husband group:none

Sponsors

Changde First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria for women 1. Age 20 years or older. 2. Undergoing cesarean delivery during the index hospitalisation. 3. At least a primary school education, with sufficient reading, writing and communication abilities to complete study procedures. 4. Provision of written informed consent. Inclusion criteria for husbands 1. Age 22 years or older; 2. The legal husband of the enrolled woman; 3. At least a primary school education, with sufficient reading, writing and communication abilities to complete study procedures; 4. No self-reported personal or family history of severe psychiatric disorders; 5. Provision of written informed consent.

Exclusion criteria

Exclusion criteria: Exclusion criteria for women 1. A self-reported personal or family history of severe psychiatric disorders. 2. Severe maternal or neonatal conditions during the index hospitalisation that, in the judgement of the clinical and research team, preclude participation or follow-up. Exclusion Criteria for Husbands: 1. Self-reported personal or family history of severe mental disorders. 2. Unable to complete surveys or follow-up due to cognitive, communication, or other reasons.

Design outcomes

Primary

MeasureTime frame
the Dyadic Coping Inventory;the Edinburgh Postnatal Depression Scale;pain at rest and movement-evoked pain;the Pain Catastrophizing Scale;

Secondary

MeasureTime frame
the Generalized Anxiety Disorder-7; the Pittsburgh Sleep Quality Index;

Countries

China

Contacts

Public ContactQi Li

Changde First People's Hospital

753190233@163.com+86 188 8722 2510

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026