Multimodal Identification of Depressive Symptoms in the Elderly
multimodal
2 other identifiers
observational
2,000
1 country
1
Brief Summary
Screening with depression scales alone is subjective, and relying on single-modal data often leads to incomplete identification of symptoms that are easily missed or misdiagnosed. In this study, we first aim to use artificial intelligence to construct a depression symptom recognition model, concatenate multimodal features such as facial expression, audio, text, and postural behavior, and deeply fuse them to construct a multimodal model.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Sep 2025
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 17, 2025
CompletedFirst Posted
Study publicly available on registry
August 8, 2025
CompletedStudy Start
First participant enrolled
September 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 30, 2027
August 11, 2025
July 1, 2025
1 year
July 17, 2025
August 7, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Use the PHQ-9 (Patient Health Questionnaire - 9 ) to assess whether the respondents have depressive symptoms. The scale score is one point for each item.
If the PHQ-9 score is 5 or higher, it is determined as a positive sign of depressive symptoms.
2025.09.01-2026.09.01
Study Arms (2)
non-depression
Elderly people without depressive symptoms
depression
Elderly people at risk of depression
Interventions
Collect the facial expressions, audio, text and postural behavior data of the respondents using electronic devices.
Eligibility Criteria
Elderly individuals aged 60 years or older
You may qualify if:
- Elderly individuals aged 60 years or older.
- Residents of the community (with residence time of more than 6 months).
- Possessing certain reading, writing and comprehension skills, being able to communicate with researchers without obstacles, and being able to independently complete the measurement of various indicators or, although unable to independently fill out the questionnaire, being able to independently make evaluations of the questionnaire items.
- Those who have given informed consent.
You may not qualify if:
- Those who meet the diagnostic criteria for cognitive impairment (dementia) as stipulated in DSM-5, and/or who suffer from severe physical diseases (such as advanced cancer, cardiovascular and cerebrovascular diseases, etc.).
- Those who are undergoing antidepressant treatment.
- Elderly individuals who have had suicidal thoughts in any psychological assessment, should be referred to the psychological hotline platform in Wuhan.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Wuhan Mental Health Center
Wuhan, Hubei, 430012, China
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Xiaoxv Yin, PhD
Huazhong University of Science and Technology
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- ECOLOGIC OR COMMUNITY
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 17, 2025
First Posted
August 8, 2025
Study Start
September 1, 2025
Primary Completion (Estimated)
September 1, 2026
Study Completion (Estimated)
December 30, 2027
Last Updated
August 11, 2025
Record last verified: 2025-07
Data Sharing
- IPD Sharing
- Will not share