RECRUITING

Preventing Suicide Among Sexual and Gender Diverse Young Adults in Primary Care

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

The overall aim of this study is to reduce suicide among sexual and gender diverse youth ages 18-24 years old. This study will compare the effectiveness of two brief suicide prevention interventions that have been adapted for use with this population to use in primary care via telehealth and will recruit youth from primary care clinics in multiple metropolitan areas. The primary study outcome is suicidal ideation. Each clinic will be randomly assigned to deliver one of the two study interventions.

Official Title

Preventing Suicide Among Sexual and Gender Diverse Young Adults in Primary Care: CRT

Quick Facts

Study Start:2023-07-13
Study Completion:2027-03
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05869552

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:18 Years to 24 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * be aged 18-24 at the time of enrollment
  2. * not have received mental health services in the past 90 days, excluding medication and case management
  3. * English-speaking
  4. * screen positive for suicide risk
  1. * are actively suicidal
  2. * have a developmental disability that would preclude them from participating in the study intervention
  3. * who are impaired due to psychosis, mania, or substance use that would prevent them from providing consent.
  4. * Participants will also be excluded at YST-III sites if they are unable to identify a minimum of one support person to participate in the intervention with them

Contacts and Locations

Study Contact

Elizabeth Arnold, PhD
CONTACT
859-562-3751
Liz.Arnold@uky.edu

Principal Investigator

Elizabeth Arnold, PhD
PRINCIPAL_INVESTIGATOR
University of Kentucky

Study Locations (Sites)

University of Pittsburgh
Pittsburgh, Pennsylvania, 15261
United States
Steve Hicks School of Social Work at the University of Texas at Austin
Austin, Texas, 78705
United States
University of Texas Southwestern Medical Center
Dallas, Texas, 75390
United States

Collaborators and Investigators

Sponsor: Elizabeth Arnold

  • Elizabeth Arnold, PhD, PRINCIPAL_INVESTIGATOR, University of Kentucky

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 Date2023-07-13
Study Completion Date2027-03

Study Record Updates

Study Start Date2023-07-13
Study Completion Date2027-03

Terms related to this study

Keywords Provided by Researchers

  • depression
  • Self-Injurious Behavior
  • sexual and gender minority youth

Additional Relevant MeSH Terms

  • Suicide
  • Suicidal Ideation