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临床试验/NCT07718022
NCT07718022招募中不适用

Relationship Abuse Prevention Intervention Implemented With Sexual and Gender Diverse Youth and Their Caregivers - Pilot Trial

University of Pittsburgh1 个研究点 分布在 1 个国家目标入组 108 人开始时间: 2026年8月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
108
试验地点
1
主要终点
Acceptability

研究概览

简要总结

This is a pilot clinical trial to test an intervention called FLARE, which is an adolescent relationship abuse prevention program for sexual and gender diverse youth and their trusted adults. FLARE comprises in-person, virtual, and asynchronous programming developed by and for caregivers and adolescents.

详细描述

In this pilot trial, the investigators will be testing FLARE, a dating violence prevention program for sexual and gender diverse youth and their trusted adults. The study will be comparing FLARE to a wait-list control. This trial will focus on assessing acceptability, feasibility, and fidelity, as well as exploratory changes in behavioral outcomes. FLARE includes 1 in-person full day session, 2 virtual large group sessions, and several asynchronous components (website, workbook, card game). FLARE runs over a 4 week period.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
14 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •SGDY eligibility includes:
  • •ages 14 to 18
  • •identifies as sexually or gender diverse (e.g., gay, lesbian, bisexual, queer, transgender, or nonbinary)
  • •uses English
  • •willing to travel to Pittsburgh for 1 in-person event; and
  • •can identify a caregiver who can also participate.
  • •Caregivers eligibility includes:
  • •age 18 or older;
  • •a caregiver of an SGDY ages 14 to 18;
  • •uses English;
  • •willing to travel to Pittsburgh for 1 in-person event; and
  • •has a child participating in this study. Caregivers can include parents or any other person whom the adolescent identifies as a trusted adult in their life. We will only enroll 1 caregiver for each SGDY; because this is a dyadic study each adolescent needs a matched participating caregiver and vice versa.

排除标准

  • •Does not meet eligibility criteria
  • •Incarcerated during the study
  • •Unable to provide verbal or REDCap consent or assent

研究组 & 干预措施

Wait list control

Other

Wait list control participants will be offered the opportunity to participate in the intervention after the investigators have completed the pilot trial

干预措施: Resource Guide (Behavioral)

FLARE intervention

Experimental

FLARE participants will receive the intervention

干预措施: FLARE (Behavioral)

结局指标

主要结局

Acceptability

时间窗: T2 (1 month post baseline)

Acceptability of Intervention Measure: Mean value of 4 items. Each question uses a five-point Likert scale for responses, coded with a value from 1 (Completely disagree) to 5 (Completely agree) and averaged to produce the mean value. The higher the computed mean value, the greater acceptability of the intervention.

Trial Feasibility

时间窗: T1 (baseline); T2 (1 month post baseline); T3 (3 months post baseline, 2 months post T2)

Trial Consent Rate: % of individuals who assented/consented to participate out of individuals who screened eligible Trial Baseline Participation Rate: % of individuals who completed the baseline survey out of individuals who assented/consented to participate Trial Intervention Demand: % of intervention arm participants who complete the intervention Trial Retention Rate: % of participants who complete each followup survey

次要结局

  • Attitudes about abusive behaviors(T1 (baseline); T3 (3 months post baseline, 2 months post T2))
  • Attitudes towards diverse identities(T1 (baseline); T3 (3 months post baseline, 2 months post T2))
  • Self-efficacy(T1 (baseline); T3 (3 months post baseline, 2 months post T2))
  • Parenting confidence(T1 (baseline); T3 (3 months post baseline, 2 months post T2))
  • Caregiver self-efficacy(T1 (baseline); T3 (3 months post baseline, 2 months post T2))
  • Motivation(T1 (baseline); T3 (3 months post baseline, 2 months post T2))
  • Resource utilization(T1 (baseline); T3 (3 months post baseline, 2 months post T2))
  • Dating related parenting monitoring(T1 (baseline); T3 (3 months post baseline, 2 months post T2))
  • Parenting monitoring(T1 (baseline); T3 (3 months post baseline, 2 months post T2))
  • LGBTQ Caregiver(T1 (baseline); T3 (3 months post baseline, 2 months post T2))
  • parent-adolescent communication(T1 (baseline); T3 (3 months post baseline, 2 months post T2))
  • Adolescent relationship abuse(T1 (baseline); T3 (3 months post baseline, 2 months post T2))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Maya Ragavan

Associate Professor of Pediatrics

University of Pittsburgh

研究点 (1)

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