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Effectiveness and feasibility of digital cognitive behavioral therapy-based intervention for children and adolescents at risk of depression: A multicenter, open-label, randomized controlled clinical trial

Effectiveness and feasibility of digital cognitive behavioral therapy-based intervention for children and adolescents at risk of depression: A multicenter, open-label, randomized controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120486
Enrollment
Unknown
Registered
2026-03-16
Start date
2026-03-16
Completion date
Unknown
Last updated
2026-03-23

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

Conditions

Depressive Symptoms (Children and Adolescents)

Interventions

Intervention Group:Digital Cognitive Behavioral Therapy (DCBT). An 8-week program with three online structured sessions per week, one lasting about 20 minutes and one lasting about 40 minutes. Core CB
Active Control Group:An eight-week program featuring three online push notifications per week delivering standardized educational materials. One session takes approximately 40 minutes to complete, and

Sponsors

Beijing Normal University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1. Aged 10-18 years; 2. Patient Health Questionnaire-9 (PHQ-9) score = 5; 3. Participants have access to mobile devices and the internet; 4. Participants have sufficient audio-visual ability to complete the project; 5. Willing to participate and provide informed consent signed by the participant and at least one parent.

Exclusion criteria

Exclusion criteria: 1. Diagnosis of psychiatric disorders (e.g., depressive disorder, anxiety disorder, bipolar disorder, schizophrenia, eating disorder, OCD); 2. Severe brain/ somatic diseases or life-threatening conditions; 3. Currently receiving any antidepressant treatment (medication, physical therapy); 4. Received psychotherapy within the past 6 months; 5. History of substance/drug abuse; 6. Known inability to complete follow-up within 5 months.

Design outcomes

Primary

MeasureTime frame
depressive symptoms;

Secondary

MeasureTime frame
anxiety symptoms;quality of life;Psychological resilience;Brief COPE Scale;Implicit Theories Measures;Stress Mindset Measure;Implementation outcome indicators;RSES;WHO-5;UCLA-3 Loneliness Scale;ISI-3;Need Satisfaction Scale;

Countries

China

Contacts

Public ContactXiaoyi Hu

Beijing Normal University (Faculty of Education)

huxiaoyi@bnu.edu.cn+86 10 5880 4088

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 3, 2026