Brief Suicidal Crisis Prevalence in Psychiatric Settings

Is this trial a fit for you?

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 aims to estimate the 12-month prevalence of brief suicidal crises in outpatient psychiatric practice and a population-based sample in the Clermont-Ferrand area. It uses a single visit per participant to collect data and self-administered questionnaires to describe the crisis and related factors. Secondary aims include describing the study population, examining factors like age and sex, and assessing psychological pain during crises of both less than and greater than 24 hours. The study is led by University Hospital, Clermont-Ferrand, and conducted at CHU de Clermont-Ferrand with no listed collaborators.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Any adult patient consulting the psychiatrist in his/her office during the recruitment period, regardless of the reason for the consultation, and who has given consent to participate in this study.

Exclusion Criteria:

* Minor patients, or patients who refuse to participate in the study.
* Patients who have already completed the self-administered questionnaires previously (e.g., a second consultation within the same week).
* Patients unable to understand and complete the self-administered questionnaires (cognitive impairment, difficulty understanding French, etc.).

Where it's running

• CHU de Clermont-ferrand
  Clermont-Ferrand, France Recruiting

Study contacts

• Study coordinator: Pierre-Michel LLORCA, prof
• Email: pmllorca@chu-clermontferrand.fr
• Phone: 33473752124

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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.