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A Long-Term Study on the Effects of Digital Taoist Psychological Intervention on Improving Adolescent Mental Health

A Study on the Intervention Effects and Mechanisms of Digital Chinese Daoist Cognitive Therapy for People with Mild to Moderate Depression/Anxiety

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128088
Enrollment
Unknown
Registered
2026-07-14
Start date
2026-11-01
Completion date
Unknown
Last updated
2026-07-20

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

Conditions

Anxiety, depression

Interventions

Intervention group:Digital Chinese Taoist Cognitive Psychotherapy group
Delayed intervention group:After a certain waiting period, try the digital Chinese Taoist cognitive therapy.
Control group:No

Sponsors

Xiangya Second Hospital, Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1.Participants aged between 16 and 18 years, with no restriction on gender; 2.No psychiatric emergency or hospitalization within the past 3 months, and no history of severe mental disorders (e.g., schizophrenia, bipolar disorder); 3.Baseline mental health status meeting the following criteria: a PHQ-9 score of 5–19 for depressive symptoms and/or a GAD-7 score of 5–14 for anxiety symptoms; 4.Participants must have the basic cognitive and learning abilities necessary to complete the study and be able to independently use a smartphone, mobile application, or mini-program; 5.Participants must have at least a junior high school education (including those currently enrolled), be native Mandarin speakers, and be able to understand the study procedures and independently complete the questionnaires; 6.Participants must voluntarily agree to participate and provide written informed consent. For those under 18 years of age, written informed consent must also be obtained from their legal guardian.

Exclusion criteria

Exclusion criteria: 1.High risk of suicide (C-SSRS = 4, or clear suicidal plan/recent serious self-harm); 2.Comorbid with severe mental disorders (e.g., major depressive disorder, bipolar disorder, schizophrenia) or with moderate-to-severe autism spectrum disorder or significant intellectual disability; 3.Initiation or adjustment of antidepressant/anxiolytic medication within the past 4 weeks, or currently receiving systematic psychotherapy (=2 sessions) that may affect intervention stability; 4.Presence of severe acute or decompensated physical illness (e.g., cardiopulmonary insufficiency, acute neurological disease, or severe organic disorder) that may affect adherence or safety; 5.Substance or alcohol abuse or dependence; 6.Contraindications for medical examinations (e.g., MRI contraindications such as metal implants in the body);

Design outcomes

Primary

MeasureTime frame
Depression symptoms;Inflammatory factors: IL-6, TNF-a, CRP, etc.;

Countries

China

Contacts

Public ContactCao Yuping

Xiangya Second Hospital, Central South University

caoyp001@163.com+86 731 8529 5240

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026