← Eichor
Study identifier: NCT06831435 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Effectiveness of Digital Cognitive Behavioral Therapy for the Treatment of Depression: a Real-world Study

Condition: Depression · Bipolar Affective Disorder · Schizophenia Disorder  ·  Sponsor: Peking University

PhaseNA
Planned participants325
Who can joinAll sexes, 14 Years to 60 Years
Healthy volunteersNo

About this study

The project proposes to develop a digital product based on cognitive behavioral therapy for the assisted treatment of depression. The digital cognitive behavioral therapy in this study is conducted based on a self-developed mobile applet. The therapy is developed by psychotherapists, which is conducted for a total of 8 weeks, with weekly sessions including AI-guided course work and homework. This study aims to evaluate the therapeutic effects of CBT-based digital products for depression in patients through a real-world study, and to explore its genetic and neuroimaging mechanisms.

This description comes directly from the study's public registry record.

Talk to the study team

Weihua Yue  ·  86-010-82805307  ·  dryue@bjmu.edu.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Peking University Sixth HostipalBeijing, Beijing Municipality, ChinaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06831435