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Clinical Trials in Taiwan / NCT07790731
Starting soon Not applicable

Using a School-Based Depression Literacy Psychoeducation Program With AI Chatbot to Improve Depression Literacy and Help-Seeking Among High School Students

NCT07790731 · tracked via the Priya Life Science Taiwan tracker
Sponsor
Chang Hsiu-Ju
Phase
Not applicable
Started
2026-08-01
Last updated
2026-08-27

Condition(s) studied

Depressive SymptomsMental Health (Depression)

Investigational drug(s) / intervention(s)

school-based depression literacy program

school-based depression literacy program: The structured psychoeducational program comprises four weekly 50-minute sessions that target knowledge of depression (causes and symptom recognition) and strategies for stigma reduction. A physical "Resource Navigation Booklet" is provided to serve as an actionable emotional first-aid kit detailing local help-seeking channels.

Study summary

The primary purpose of this randomized controlled trial is to evaluate the effectiveness of an AI chatbot enhanced school-based depression literacy psychoeducational program, combined with a resource navigation booklet, on high school students in Taiwan.

Despite the high prevalence of depression among adolescents, the treatment gap remains significantly large due to low mental health literacy and high stigma. This study aims to bridge this gap by implementing a 4-week structured psychoeducational intervention. The investigators hypothesize that participants in the experimental group will demonstrate a significant improvement in depression literacy, a reduction in stigmatizing attitudes toward depression, and more positive attitudes toward seeking professional psychological help compared to those in the control group (regular classes as usual). Outcomes will be assessed at baseline and immediately post-intervention.

Eligibility

Sex
ALL
Min age
15 Years
Max age
19 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Students aged 15 to 19 enrolled in participating high schools in Taiwan. Fluent in speaking, reading, and writing traditional Chinese, capable of independently completing self-report questionnaires. Willing to participate and provide signed informed assent, alongside signed informed consent from a parent or legal guardian. Exclusion Criteria: * Diagnosed with severe cognitive impairment or developmental delay that prevents understanding the curriculum or completing the questionnaires. Currently experiencing an acute psychiatric crisis or exhibiting high risk for self-harm/suicide (e.g., active suicidal ideation, or scoring \>= 15 on the baseline Patient Health Questionnaire-9 \[PHQ-9\], or scoring \>= 1 on item 9 of the PHQ-9). These individuals will be referred to immediate standard psychiatric or school counseling care.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
National Yang Ming Chiao Tung University Taipei Taiwan

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07790731 on ClinicalTrials.gov ↗ ← All trials in Taiwan