Trauma Exposure and Suicide prevention in Adolescents Aged 11-17 Hospitalized in Child and Adolescent Psychiatry
This study is not yet recruiting. It focuses on suicide prevention and currently lists study information in Global.
Key information made simple
What is this study testing?
This study is testing whether Blood samples may be useful for adolescents experiencing suicide prevention.
What would participation involve?
Participants may complete study activities around Blood samples, complete questionnaires or follow-up assessments, provide blood samples or biological tests.
Who is it mainly for?
This study appears to be mainly for adolescents with suicide prevention. Because it involves minors, a parent or guardian may need to be involved.
What should you check before joining?
Ask about whether there is a comparison group, how many visits or travel steps are needed, what role parents or guardians have in the process.
Your next step
The official record does not clearly describe the visit format, so the practical details are best checked directly in the source. Participation appears to involve study activities and follow-up chosen by the research team. The main fit and exclusions are best confirmed in the eligibility section of the official record. The phase details are not clearly stated here.
Questions to ask before joining
- What are the exact eligibility criteria, and what could exclude someone?
- How many visits, assessments, or follow-ups are expected, and over what period?
- What risks, side effects, practical burdens, or alternatives should be understood first?
- Who should be contacted to confirm locations, timing, compensation, and next steps?
Things to check before joining
- Recruitment status
- Not Yet Recruiting
- Estimated enrollment
- 120
- Sponsor
- University Hospital, Montpellier
- Sponsor type
- Hospital / academic medical center
- Study type
- Biological
- Intervention type
- BIOLOGICAL, GENETIC, OTHER
- Study phase
- Not clearly listed
- Locations
- Global
- Age range
- From 11 Years to 17 Years
- Official registry ID
- NCT07430566
- Official title
- Trauma Exposure and Suicidal Behaviors in Adolescents Aged 11-17 Hospitalized in Child and Adolescent Psychiatry
- Official source
- Official registry link
Want help reviewing this study?
For you
Taking part may give access to a new approach being evaluated.
It requires regular follow-up, often through questionnaires or interviews.
Not medical advice
Information from public sources. Are you the study sponsor? Contact us to update this page: hi@hopestage.com
Questions about this study
What is this study trying to understand?
Based on the public registry summary, this study is trying to understand: It is a comparative monocentric study with longitudinal follow-up at 6 months in adolescents aged between 11 years and 17 years inclusive admitted to complete hospitalization either for suicidal behaviors or for other psychiatric causes. The objective is to explore the. The study team can confirm the exact objective and what it means for you.
Does this study involve biological samples, imaging, or biomarkers?
This appears to be a biological / biomarker / imaging study involving Blood samples, genetic analysis, Questionnaires and scales. The phase is not clearly listed in the public registry. Phase is mostly relevant for medication studies and some device studies. For this study, it may be more useful to look at what is required, the duration, visits, and eligibility criteria.
Who might this study be for?
This study may concern people with suicide prevention; age range: From 11 Years to 17 Years. The criteria appear strict, but you should not assume you are eligible. The study team must confirm diagnosis, age, exclusions, available locations, and next steps.
What would I likely need to do?
You may need to provide biological samples, complete lab tests, or take part in imaging or measurement procedures. The listed study locations suggest that at least part of participation may involve a physical site. Ask whether some steps can be done remotely.
What should I check about samples, imaging, data, and possible discomfort?
If the study involves samples, imaging, or biomarkers, ask what is collected, how it is stored, who can access results, whether there may be discomfort, and whether results are shared with you. For any mental health study, also ask who to contact if you feel worse, whether participation may affect current treatment, whether you can stop, and who confirms eligibility.
Will I need to travel or attend in-person visits?
The listed study locations suggest that at least part of participation may involve a physical site. Ask which sites are open, how many visits are expected, whether any steps can be done remotely, and whether travel costs or compensation are listed.
Who is behind this study?
This study is sponsored by University Hospital, Montpellier, which appears to be a hospital or academic medical center. If available, it can be useful to check the sponsor website, collaborators, investigator affiliation, and the official registry before deciding. HopeStage does not judge the quality of a sponsor or researcher, but helps you identify what to verify.
Can I still join this study?
The registry indicates that this study has not started recruiting yet. You can check the planned start date and available contacts. The registry lists an estimated enrollment of 120 participants.
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