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Machine Learning-based Classification of Symptom Clusters and Online CBT

Machine Learning-based Classification of Symptom Clusters and Matched Online Cognitive Behavior Intervention for Depression Symptom and Anxiety Symptom

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06350201
Enrollment
409
Registered
2024-04-05
Start date
2025-09-01
Completion date
2026-12-01
Last updated
2026-09-08

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

Conditions

Depression and Anxiety Symptom

Keywords

machine learning approach, CBT, PST, depression, anxiety

Brief summary

To breakthrough the bottleneck identified, we will conduct a cross-sectional study to develop a symptom clustering model for depression and anxiety. A wide range of statistical methods as well as machine learning approaches were explored, and a cohesive hierarchical clustering algorithm will be used. After developing the model, a symptom-matched intervention program based on problem solving therapy will be formulated. We are supposed to examine whether its use for personalizing symptom-matched psychological treatment can lead to improved patient outcomes, compared with usual care. This project is expected to provide a new and precise method for the emotion management, which will provide a standardized intervention pathway combining screening with treatment for the management of depression symptom and anxiety symptom. A preciser intervention matched to individual symptoms may provide important insight in improving patient outcome as well as a standardized mood management pathway targeting to the early detection and intervention for community residents.

Interventions

BEHAVIORALproblem solving therapy

Problem-solving therapy-based holistic emotion management interventions matched to individual symptoms

OTHERcontrol group

Routine psychological care and guidance on mood management

Sponsors

Wuhan Mental Health Centre
Lead SponsorOTHER
National Natural Science Foundation of China
CollaboratorOTHER_GOV
Renmin Hospital of Wuhan University
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

* Aged between 18 and 64 years. PHQ-9 ≥10 and/or GAD-7 ≥8 at baseline assessment defined as the threshold for caseness.

Exclusion criteria

* People will be excluded if they meet any of the following criteria: 1. They are receiving psychological therapy during an interview for any mental health issue; 2. currently acutely suicidal or have attempted suicide in the past 2 months, as indicated by PHQ-9 item 9; 3. cognitively impaired or diagnosed with bipolar disorder or psychosis or experiencing psychotic symptoms; d) dependent on alcohol or drugs; e) living with an unstable or acute medical illness that would interfere with trial participation.

Design outcomes

Primary

MeasureTime frame
The Patient Health Questionnaire (PHQ-9)Baseline, week 1, week 2, week 3, week 4, week 5, week 6, week 7, week 8, week 12, week 20, week 32
GAD-7Baseline, week 1, week 2, week 3, week 4, week 5, week 6, week 7, week 8, week 12, week 20, week 32

Secondary

MeasureTime frame
PSQIBaseline, week 1, week 4, week 6, week 8, week 12, week 20, week 32
WHODAS 2.0Baseline, week 1, week 4, week 6, week 8, week 12, week 20, week 32
EQ-5D-5LBaseline, week 1, week 4, week 6, week 8, week 12, week 20, week 32

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 9, 2026