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Cancelled by the investigator. Digital health-based psychological intervention in pregnant women with adverse childhood experiences

Digital health-based psychological intervention in pregnant women with adverse childhood experiences

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124814
Enrollment
Unknown
Registered
2026-05-18
Start date
2026-05-22
Completion date
Unknown
Last updated
2026-07-20

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

Conditions

Prenatal depression

Interventions

Intervention group:At baseline, participants will receive a link to an online platform and undergo a 12-week EMI-CBT intervention delivered via a WeChat mini program. During the 12-week period, the sy
Control group:Participants will receive routine obstetric care. To minimize loss to follow-up, the research team will send monthly reminder text messages regarding upcoming follow-up assessments.

Sponsors

Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years, Chinese nationality, and able to speak fluent Mandarin; 2. Gestational age =1 on the Adverse Childhood Experiences (ACEs) International Questionnaire; 4. Receiving regular prenatal care at a hospital; 5. Ownership of at least one smartphone; Provided informed consent, willing to participate voluntarily, and able to comply with follow-up.

Exclusion criteria

Exclusion criteria: 1. Clinically diagnosed depression or other psychiatric/behavioral disorders; 2. Presence of severe physical illness.

Design outcomes

Primary

MeasureTime frame
Prenatal depression level;

Secondary

MeasureTime frame
Feasibility;Acceptability;

Countries

China

Contacts

Public ContactLijuan Wang

Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine

722004016@shsmu.edu.cn+86 134 8207 7053

Outcome results

None listed

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