Evaluating a suicide risk screening program in rural schools
Implementing the NIMH Clinical Pathway in Rural Appalachian School-based Health Clinics
NA · West Virginia University · NCT06808503
This study is testing a new program in rural West Virginia schools to see if it can help identify and support students at risk of suicide.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 30 (estimated) |
| Ages | 12 Years to 17 Years |
| Sex | All |
| Sponsor | West Virginia University (other) |
| Locations | 1 site (Morgantown, West Virginia) |
| Trial ID | NCT06808503 on ClinicalTrials.gov |
What this trial studies
This study adapts and evaluates the NIMH Clinical Pathway, an evidence-based program for suicide risk screening, in two school-based health centers in West Virginia. The program includes tools for screening adolescents for suicide risk, conducting risk assessments, safety planning, and follow-up referrals. Investigators will gather formative data from providers, parents, and youth to tailor the program for effective implementation in rural Appalachian settings, as well as preliminary data on its feasibility, acceptability, and effectiveness.
Who should consider this trial
Good fit: Ideal candidates include English-speaking youth receiving services at the school-based health centers, along with their parents who can provide consent.
Not a fit: Youth in state custody will not benefit from this study due to legal consent challenges.
Why it matters
Potential benefit: If successful, this program could significantly improve suicide prevention efforts among adolescents in rural areas.
How similar studies have performed: Other studies have shown success with similar suicide prevention approaches, indicating potential for effective adaptation in this context.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Youth who are receiving services at the school-based health centers to participate * Parents must be able to give legal consent for themselves and their children to participate * Youth and Parent must be English-speaking * Youth must also be able to give signed assent to participate * Youth must be cognitively and medically able to participate in study activities Exclusion Criteria: * Youth in state custody will be excluded from study participation due to challenges related to obtaining legal consent.
Where this trial is running
Morgantown, West Virginia
- West Virginia University — Morgantown, West Virginia, United States (RECRUITING)
Study contacts
- Principal investigator: Mary Christensen, PhD, LICSW — West Virginia University
- Study coordinator: Mary Christensen, PhD, LICSW
- Email: mary.christensen@mail.wvu.edu
- Phone: 304-293-3501
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Suicide Prevention, Suicide