Actively Recruiting
Eco-anxiety and Severity of Suicide Risk in Adolescents Aged 12 to 16
Led by Hospices Civils de Lyon · Updated on 2025-01-06
261
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating the link between eco-anxiety and suicide risk in adolescents aged 12 to 16 who are hospitalized for mental health reasons. Suicide is a major public health concern, particularly among young people, and anxiety related to climate change, known as eco-anxiety, may influence suicidal thoughts and behaviors. This study aims to better understand how eco-anxiety relates to the severity of suicide risk using validated scales. Participants will complete three questionnaires: the 13-item Climate Anxiety Scale (CAS) to measure eco-anxiety, the Columbia-Suicide Severity Rating Scale (C-SSRS) to assess suicide risk, and the Hospital Anxiety and Depression Scale (HAD). These assessments help evaluate cognitive, emotional, behavioral, and functional aspects related to climate anxiety and suicide risk. The study involves a single group of adolescents hospitalized in a specialized child and adolescent psychiatry department. During the study, participants will fill out these scales once at inclusion to measure the intensity of eco-anxiety and the severity of suicide risk. The research team will analyze the relationship between these factors to identify potential risk patterns. Participation includes completing questionnaires in French and involves monitoring mental health status. The total participation duration corresponds to the initial assessment time, with no additional interventions or follow-up visits planned.
CONDITIONS
Brief Title
Eco-anxiety and Suicide
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adolescents aged 12 to 16 years
- Hospitalized at the Hopital Femme Mère Enfant in the child and adolescent psychopathology department
You will not qualify if you...
- Does not speak French
- Unable to read or write
- Intellectual development or oral comprehension disorders that prevent understanding or reading
- Oral or written refusal by the parents or the child
- Not affiliated with a social security system and under legal protection
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - At the inclusion
Participants complete three assessment scales to evaluate eco-anxiety intensity and suicide risk severity.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
Hôpital Femme Mère Enfant
Bron, Rhone, France, 69500
Actively Recruiting
Research Team
C
Christophe Gauld, Dr
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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