RECRUITING

NIMH Clinical Pathway in Rural Appalachian School-based Health Clinics

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Implementing the NIMH Clinical Pathway in Rural Appalachian School-based Health Clinics

Quick Facts

Study Start:2024-10-02
Study Completion:2026-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06808503

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:12 Years to 17 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. * Youth who are receiving services at the school-based health centers to participate
  2. * Parents must be able to give legal consent for themselves and their children to participate
  3. * Youth and Parent must be English-speaking
  4. * Youth must also be able to give signed assent to participate
  5. * Youth must be cognitively and medically able to participate in study activities
  1. * Youth in state custody will be excluded from study participation due to challenges related to obtaining legal consent.

Contacts and Locations

Study Contact

Mary Christensen, PhD, LICSW
CONTACT
304-293-3501
mary.christensen@mail.wvu.edu

Principal Investigator

Mary Christensen, PhD, LICSW
PRINCIPAL_INVESTIGATOR
West Virginia University

Study Locations (Sites)

West Virginia University
Morgantown, West Virginia, 26505
United States

Collaborators and Investigators

Sponsor: West Virginia University

  • Mary Christensen, PhD, LICSW, PRINCIPAL_INVESTIGATOR, West Virginia University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-10-02
Study Completion Date2026-06

Study Record Updates

Study Start Date2024-10-02
Study Completion Date2026-06

Terms related to this study

Additional Relevant MeSH Terms

  • Suicide Prevention
  • Suicide