Efficacy of an internet-based cognitive behavioral intervention for psychological distress for pregnant women and postnatal maternal and infant health: a case-control trial

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2300069470

Enrollment

Unknown

Registered

2023-03-17

Start date

2023-04-10

Completion date

Unknown

Last updated

2023-05-29

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

Conditions

depression, anxiety

Interventions

experimental group:CBT

case-control group:null

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: 1. Aged 20 years or older; 2. Currently being pregnant 3. DASS-21 depressive symptom score > 10, anxiety symptoms score > 8, or stress levels score > 15; 4. Provided informed consent.

Exclusion criteria

Exclusion criteria: 1. Has been diagnosed with any of depressive disorder, generalized anxiety disorder, bipolar disorder, substance dependence and substance abuse, anti-social personality disorder, or post-traumatic stress disorder within the past year; 2. Taking anti-depression and anti-anxiety drugs within the past 3 months; 3. Receiving other types of (individual/group) psychological counseling or intervention.

Design outcomes

Primary

Measure	Time frame
Depression Anxiety Stress Scale-21 (DASS-21) score;	—

Secondary

Measure	Time frame
satisfaction of the intervention;maternal obstetric outcomes;neonatal health outcomes;mother-infant care;infant regulation;	—

Countries

China

Contacts

Public ContactGuangyu Zhou

School of Psychological and Cognitive Sciences and Beijing Key Laboratory of Behaviour and Mental Health, Peking University

gyzhou@pku.edu.cn+86 10 62751820

Outcome results

None listed

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