The effectiveness evaluaton of Intervention model of perinatal depression in women with fetal anomaly

Study of intelligent management system for perinatal depression in women with fetal anomaly to the direction of big data healthcare

Status

Recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100047195

Enrollment

Unknown

Registered

2021-06-10

Start date

2021-07-01

Completion date

Unknown

Last updated

2022-01-24

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

Conditions

depression

Interventions

Experimental group:Perinatal depression intervention program

Control group:Routine nursing

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: 1.Women diagnosed with fetal abnormalities; 2.Depression screening was positive (EPDS>=10); 3.Those who can use a smartphone; 4.No language barrier, able to understand the questionnaire, willing to participate in this study.

Exclusion criteria

Exclusion criteria: 1.Choose to continue the pregnancy; 2.Those who choose to have labor induced in a hospital other than three; 3.Have serious life-threatening complications (including heart failure, eclampsia, severe preeclampsia, haemorrhagia, etc.); 4.People with serious mental illness (suicidal tendency or serious mental illness diagnosed by a psychiatrist); 5.Who have relevant psychotherapy training experience.

Design outcomes

Primary

Measure	Time frame
depression;	—

Secondary

Measure	Time frame
Post-traumatic Stress Symptoms;psychological flexibility;	—

Countries

China

Contacts

Public ContactQin Chunxiang

Third Xiangya Hospital of Central South University

Chunxiangqin@csu.edu.cn+86 13469072193

Outcome results

None listed

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