NIMH Clinical Pathway in Rural Appalachian School-based Health Clinics

Part of paid clinical trials in Morgantown, West Virginia.

Sponsor
West Virginia University
Study ID
NCT06808503
Status
Recruiting

Conditions

  • Suicide
  • Suicide Prevention

Eligibility Criteria

Sex
ALL
Age
12 Years - 17 Years
Healthy Volunteers
Accepted

Interventions

  • NIMH Clinical Pathway — BEHAVIORAL
    Complete the implemented workflow and tools for suicide risk screening, assessment, safety planning and follow-up.

Study Details

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, completing risk assessments, safety planning, lethal means restriction, follow-up referrals, and other disposition planning as appropriate. Investigators aim to do the following: 1. Gather formative data from providers, parents, and youth to inform ways to adapt and implement the NIMH Clinical Pathway so that it can be effectively implemented in rural, Appalachian School-Based Health Centers (SBHCs). 2. Gather preliminary data regarding the feasibility, acceptability, and effectiveness of the adapted intervention.

Key Dates

Start date
Oct 2, 2024
Status verified
Apr 2026
Primary completion
May 31, 2027
Completion
May 31, 2027

Study Design

Enrollment
30 participants (estimated)
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING

Arms

  • No Intervention: Treatment As Usual (TAU)
    Review all medical records for patients for the standard of care used at the facility for suicide assessment and risk. Determine if the enrolled patients were assessed and if risks are present.
  • Active Comparator: NIMH Clinical Pathway
    Implementation of an adapted/tailored version of the NIMH Clinical Pathway, which identifies a workflow and tools for routine suicide risk screening, assessment, safety planning and follow-up.

Primary Outcome Measure

Number of Patients Screened for Suicidal Risks-Site 1 [ Time Frame: Total period of 3 Months ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
West Virginia UniversityMorgantownWest Virginia26505
Mary Christensen, PhD, LICSW
304-293-3501
Mary Christensen, PhD, LICSW (PRINCIPAL_INVESTIGATOR)

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