What this study is
This study will adapt and evaluate an evidence-based suicide risk screening and follow-up program in two school-based health centers in West Virginia. The suicide screening program is titled the "NIMH Clinical Pathway" and provides tools and procedures for routinely screening adolescents for suicide risk screening, suicide risk assessment, safety planning, referral procedures, and follow-up care activities for adolescents receiving health services.
The study will assess implementation outcomes, including suicide screening practices, identification of suicide risk, safety planning, and follow-up service delivery, as well as participant outcomes including suicidal ideation, depressive symptoms, satisfaction with services, suicidal behavior, safety plan utilization, and acute care utilization. Data collected across participating sites will be combined to evaluate the feasibility, acceptability, and preliminary effectiveness of the adapted Clinical Pathway. Protocol amendments resulted in consolidation of site-specific outcome measures into combined analyses across participating school-based health centers. The ClinicalTrials.gov record was updated to reflect the current protocol, study procedures, and planned statistical analyses.
What's being tested
- NIMH Clinical Pathway
Intervention · BEHAVIORAL
Complete the implemented workflow and tools for suicide risk screening, assessment, safety planning and follow-up.
Study details
- Official title
- Implementing the NIMH Clinical Pathway in Rural Appalachian School-based Health Clinics
- Sponsor
- West Virginia University
- Conditions
- Suicide Prevention · Suicide
- Enrolling
- 70 people
- Starts
- 2024-10-02
- Est. completion
- 2027-08
- Design
- Open-label, non-randomized, single group
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 12 Years – 17 YearsSex ALLHealthy volunteers AcceptedYou may qualify if
- 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
You can't join if
- Youth in state custody will be excluded from study participation due to challenges related to obtaining legal consent.
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (3)
3 openContact for every open site
- Mary Christensen, PhD, LICSW · Contact304-293-3501mary.christensen@mail.wvu.edu
West Virginia University
Morgantown, West Virginia, United States
- Mary Christensen, PhD, LICSW · Principal investigator
RecruitingOak Hill School Based Health Center
Oak Hill, West Virginia, United States
RecruitingSummersville School Based Health Center
Summersville, West Virginia, United States
Recruiting
Study team
Sponsor
West Virginia University
Study ID 2405972188
Principal investigator
Mary Christensen, PhD, LICSW
West Virginia University
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.