Clinical trial Recruiting at 1 site Observational Ages 16 to 60

Suicide risk and learned suicide ability in people with mood disorders

Official title: Investigation on Suicide Risk Factors of Patients With Mood Disorders in China

Run by Tianjin Anding Hospital · NCT07523490 · Data updated 2026-11-12

This project will try to identify which biological, psychological, social, and clinical factors relate to suicide risk and the learned ability for suicide in people aged 16–60 with mood disorders by collecting blood, urine, and questionnaire data.

Quick facts

Study typeObservational
Ages16 Years to 60 Years
SexAll
Enrollment300 (estimated)
SponsorTianjin Anding Hospital
Academic / other
Locations1 site (Tianjin, Tianjin Municipality)
StatusRecruiting
StartedDecember 31, 2025
Main results expectedSeptember 30, 2027
Study endsSeptember 30, 2027
Registry record updatedApril 22, 2026
Trial IDNCT07523490 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal participants are people aged 16–60 who are receiving psychiatric care, meet ICD‑11 mood disorder criteria, are willing to cooperate, and can provide informed consent (guardian consent required for minors).

Probably not a fit

Patients with serious organic illnesses that prevent participation, those unable to understand or complete questionnaires, or people without a mood disorder are unlikely to benefit from this project.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study enrolls people aged 16–60 who meet ICD‑11 criteria for mood disorders at Tianjin Anding Hospital. Participants complete standardized scales (Beck Scale for Suicide Ideation, Columbia Suicide Severity Rating Scale, HAMD, HAMA, PHQ‑9, GAD‑7 and functional measures) and provide blood and urine samples for molecular biomarker analysis. Investigators will analyze biological, psychological, social, and clinical data to identify factors tied to suicide risk and the formation of learned suicide ability and will develop a prediction model. No treatments are assigned; the aim is to produce a ranked list of risk factors and a validated predictive tool for learned suicide ability.

Why it matters

Potential benefit: If successful, this work could help clinicians identify patients at higher risk of suicide earlier and tailor prevention efforts more effectively.

How similar studies have gone: Previous multi-dimensional studies have had some success identifying suicide risk markers and building predictive models, but prediction of 'learned suicide ability' is relatively novel and requires more validation.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Age: 16 to 60 years old;
2. seeing a doctor in a psychiatric clinic or a general hospital;
3. Willing to cooperate in this research project;
4. Sign the informed consent form (minors also need to obtain the informed consent signature of the guardian);
5. Meet the diagnostic criteria of ICD-11 mood disorder.

Exclusion Criteria:

1. unable to understand the contents of the questionnaire;
2. Serious organic diseases such as cardiovascular disease, brain disease, liver disease and kidney disease, and weak body, which affect the respondents of the questionnaire;
3. Other circumstances that make it impossible or unwilling to cooperate with the completion of the questionnaire.

Where it's running

  • Tianjin Anding Hospital
    Tianjin, Tianjin Municipality, China
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.