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Development and verification of AI conversational cognitive behavior intervention products for anxious people

Development and verification of AI conversational cognitive behavior intervention products for anxious people

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099437
Enrollment
Unknown
Registered
2025-03-24
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-03-31

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

Conditions

Anxiety Disorders

Interventions

Research Intervention Group for Social Anxiety Disorder:The research intervention group implemented a semi-open AI dialogue-based CBT self-help intervention in conjunction with conventional treatment.
Research Intervention Group for Panic Disorder:The research intervention group implemented a semi-open AI dialogue-based CBT self-help intervention in conjunction with conventional treatment. This CBT
Research Intervention Group for Generalized Anxiety Disorder:The research intervention group implemented a semi-open AI dialogue-based CBT self-help intervention in conjunction with conventional treat
Social Anxiety Disorder Conventional Treatment Group:Clinical guidelines for anxiety disorders advocate for intervention plans, excluding diverse forms of CBT
Panic Disorder Conventional Treatment Group:Clinical guidelines for anxiety disorders

Sponsors

Beijing Anding Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria for Social Anxiety Disorder: 1. Currently meets the diagnostic criteria for DSM-5 Social Anxiety Disorderr; 2. Gender: open to all, age range: 16-60 years, with a minimum education level of junior high school; 3. Has not undergone systematic cognitive-behavioral therapy within the 6 months preceding enrollment; 4. Capable of using smartphones, tablets, or other internet-enabled devices without any impediments; 5. The patient must sign the informed consent form, and for those under 18 years of age, a guardian's signature on the informed consent form is also required. Inclusion Criteria for Panic Disorder: 1. Currently meets the diagnostic criteria for DSM-5 Panic Disorder; 2. Gender: open to all, age range: 16-60 years, with a minimum education level of junior high school; 3. Has not undergone systematic cognitive-behavioral therapy within the 6 months preceding enrollment; 4. Capable of using smartphones, tablets, or other internet-enabled devices without any impediments; 5. The patient must sign the informed consent form, and for those under 18 years of age, a guardian's signature on the informed consent form is also required. Inclusion Criteria for Generalize Anxiety Disorder: 1. Currently meets the diagnostic criteria for DSM-5 Generalize Anxiety Disorder; 2. Gender: open to all, age range: 16-60 years, with a minimum education level of junior high school; 3. Has not undergone systematic cognitive-behavioral therapy within the 6 months preceding enrollment; 4. Capable of using smartphones, tablets, or other internet-enabled devices without any impediments; 5.The patient must sign the informed consent form, and for those under 18 years of age, a guardian's signature on the informed consent form is also required.

Exclusion criteria

Exclusion criteria: 1. Currently or previously diagnosed with other severe mental disorders and neurodevelopmental disorders that meet the DSM-5 diagnostic criteria, including schizophrenia, bipolar affective disorder, mental retardation, etc.; 2. Currently suffering from substance addictions such as alcohol and drugs, as well as non-substance addictions like online gaming; 3. HAMD-17 score greater than 17 or at risk of suicide (HAMD-17 item 3 scale score greater than 2); 4. Currently has severe physical illnesses that researchers believe are not suitable for inclusion in this study; 5. Any other situations that researchers consider unsuitable for inclusion.

Design outcomes

Primary

MeasureTime frame
Hamilton Anxiety Scale,HAMA;Panic Disorder Severity Scale,PDSS;Liebowitz social anxiety scale, LSAS;

Secondary

MeasureTime frame
clinical global impression scale,CGI;Generalized Anxiety Disorder Scale,GAD-7;self-rating anxiety scale,SAS;Hamilton Depression Scale,HAMD;Social Interaction Anxiety Scale, SIAS;Social Phobia Scale, SPS;World Health Organization Quality of Life-Brief, QOL-BREF;Patient Health Questionnaire-9, PHQ-9;The State-Trait Anxiety Inventory, STAI;Anxiety Sensitivity Index-3, ASI-3;Irrational Beliefs Inventory, IBI;Ruminative Responses Scale - Chinese Version, RRS-CV;Chinese Cognitive Emotion Regulation Questionnaire, CERQ-C;Acceptance and Action Qwestionnaire, AAQ-II;

Countries

China

Contacts

Public ContactLi Zhanjiang

Beijing Anding Hospital, Capital Medical University

lizhj8@ccmu.edu.cn+86 137 0121 8860

Outcome results

None listed

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