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Идёт набор NCT05869552

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

Без фазы С лечением Suicide Suicidal Ideation

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: STAT-PC, YST-III.
Кому может быть актуально
Состояния в реестре: Suicide, Suicidal Ideation. Базовые параметры: 18 лет — 24 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
США
Следующий шаг
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Официальное название

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

Обзор

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.

Вмешательства

  • Другое STAT-PC
    STAT-PC is an adapted version of Suicidal Teens Accessing Treatment after an ED Visit (STAT-ED). It is a brief intervention based on motivational interviewing (MI) that focuses on mental health care seeking behavior, problem-solving, and referrals plus brief case management. The intervention will consist of an initial session with the youth focusing on accessing mental health care plus case management calls. The interventionist will also be available to assist with referrals for connection to ot
  • Другое YST-III
    YST-III is an adapted version of Youth-Nominated Support Team for Suicidal Adolescents (YST-II). The intervention is a brief intervention originally developed for youth who have been psychiatrically hospitalized due to a suicide attempt or suicidal ideation (SI). Participants will nominate supportive adults (age 18 and older) from their lives who agree to provide ongoing contact and support for up to 3 months. YST-III will include an introductory session with the youth who will nominate their su

Первичные конечные точки

  • Change in suicidal ideation as measured by the Adult Suicidal Ideation Questionnaire (ASIQ) [Срок оценки: baseline and months 1, 3, 6]
Вторичные конечные точки (6)
  • Change in number of mental healthcare service utilization as measured by Emergency Department Screen for Teens at Risk for Suicide (ED-STARS) mental health service utilization check list [Срок оценки: baseline and months 1, 3, 6]
  • Change in number of suicide attempts [Срок оценки: baseline and months 1, 3, 6]
  • Deaths by suicide [Срок оценки: baseline to 6 months]
  • Change in depressive symptoms as measured by Center for Epidemiologic Studies Depression Scale-Revised CESD-R [Срок оценки: baseline and months 1, 3, 6]
  • Change in social support as measured by the Multidimensional Scale of Perceived Social Support (MSPSS) [Срок оценки: baseline and months 1, 3, 6]
  • Change in internalized stigma as measured by Internalized Transphobia Scale (ITS)-adapted [Срок оценки: baseline and months 1, 3, 6]

Критерии участия

Критерии включения

  • be aged 18-24 at the time of enrollment
  • not have received mental health services in the past 90 days, excluding medication and case management
  • English-speaking
  • screen positive for suicide risk

Критерии исключения

  • are actively suicidal
  • have a developmental disability that would preclude them from participating in the study intervention
  • who are impaired due to psychosis, mania, or substance use that would prevent them from providing consent.
  • 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

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Лечение

Центры проведения

США · 3 центра
  • University of Pittsburgh — Pittsburgh
  • Steve Hicks School of Social Work at the University of Texas at Austin — Austin
  • University of Texas Southwestern Medical Center — Dallas

Идентификаторы

NCT: NCT05869552 · 86014 · SP-2020C3-21020-IC

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗