Application of self-help mental health assessment and intervention technology based on AI in physical examination

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2400080463

Enrollment

Unknown

Registered

2024-01-30

Start date

2024-02-05

Completion date

Unknown

Last updated

2024-02-05

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

Conditions

psychological subhealth

Interventions

Study 1: Observation Group:NA

Study 2: Control group:Health Education

Study 2: Experimental Group:AI assisted Psychological Assessment and Treatment system, AiPAT

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Study 1: Identification and screening of psychological subhealth individuals: ? Chinese residents who voluntarily participated in the study; ? Age 18 and above; ? Familiar with Mandarin, including listening and reading/writing abilities; ? Familiar with using smartphones and mobile networks; ? Participants are required to submit informed consent online. Study 2: Interventional efficacy of AiPAT on psychological subhealth: ? Chinese residents who voluntarily participated in the study; ? Age range from 18 to 65 years old, suitable for diagnosis of psychological subhealth population; ? Meets PHQ-9:5-14, GAD-7:5-14, or ISI: 8-21; ? Proficient in Mandarin, including listening and reading/writing abilities; ? Proficient in using smartphones and mobile networks; ? Agree to accept non pharmacological intervention; ? Anxiety and depression persist for 2 weeks or more, or sleep difficulties persist for more than a month.

Exclusion criteria

Exclusion criteria: Study 1: No special exclusion criteria were set Study 2: ? For individuals with suicidal behavior and ideation, the suicide score in PHQ-9 is greater than 0; ? Material dependence history (excluding tobacco dependence); ? Pregnant or lactating women; ? Individuals who have received and/or have previously received cognitive behavioral interventions related to depression, anxiety, and insomnia; ? Meets the diagnostic criteria for clinical depression, anxiety disorders, and sleep disorders.

Design outcomes

Primary

Measure	Time frame
Patient Health Questionnaire-9,PHQ-9;GeneralizedAnxietyDisorder,GAD-7;Insomnia Severity Index, ISI;	—

Secondary

Measure	Time frame
Pittsburgh Sleep Quality Index,PSQI;The Altman Self-Rating Mania Scale, ASRM;Connor-Davidson Resilience Scale,CD-RISC;Social Support Rating Scal,SSRS;Heart Rate Variability;	—

Countries

China

Contacts

Public ContactShuping Tan

Beijing Huilongguan Hospital

shupingtan@126.com+86 10 8302 4485

Outcome results

None listed

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