跳至主要内容
临床试验/NCT06638853
NCT06638853进行中(未招募)不适用

The STRIDE Study (Strengthening Tolerance and Resilience in Dealing with Emotions): Pilot Testing of a School-Based Distress Tolerance Skills Program for Reducing Risk of Psychopathology in Adolescence

Oregon Health and Science University2 个研究点 分布在 1 个国家目标入组 74 人开始时间: 2024年10月25日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
74
试验地点
2
主要终点
Feasibility

研究概览

简要总结

Research suggests that an individual's perceived ability to withstand distressing or upsetting emotions (i.e., distress tolerance; DT) is a common risk factor across several mental health conditions that commonly emerge during adolescence. This study aims to evaluate the acceptability, feasibility, and initial efficacy of a classroom-based DT skills training program for middle school students. This study will also explore associations between changes in DT and internalizing symptoms (e.g., anxiety, depression).

详细描述

A variety of deleterious mental health conditions have their peak age of onset in adolescence, including depression and anxiety. Distress tolerance (DT) - defined as the perceived or actual ability to withstand aversive emotional states - has been postulated as a transdiagnostic risk factor across several "emotional" disorders that typically emerge during adolescence. Importantly, while there is compelling evidence that DT is associated with emotion dysregulation and symptom severity, it is unclear whether modifying DT can reduce future risk for psychopathology in adolescent populations. This proposal aims to evaluate the feasibility, acceptability, and initial efficacy of a classroom-based DT intervention for middle school students. Additionally, this proposal will examine associations between changes in DT and internalizing symptoms.

Primary Objective:

To evaluate the acceptability, feasibility, and efficacy of a classroom-based DT skills training program for middle school students.

Secondary Objectives:

To examine whether participation in the DT skills training program is associated with lower severity of internalizing symptoms over the course of the academic year.

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
11 Years 至 14 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Middle school aged-youth attending Valley Catholic Middle School in grade 6, 7, or 8

排除标准

  • 未提供

结局指标

主要结局

Feasibility

时间窗: Pre-intervention and immediately post-intervention

Consent rates during enrollment and attrition rates during the study will be used to assess the feasibility of the intervention.

Acceptability

时间窗: Immediately post-intervention

The investigators will use a brief feedback survey at the end of the study to gather information about participants' experiences of the intervention. Responses on this survey will be used to determine the acceptability of the intervention.

Distress Tolerance

时间窗: Pre-intervention, immediately post-intervention, 3-month follow-up, and 6-month follow-up

The investigators will assess change in distress tolerance from pre-intervention to post-intervention. Distress tolerance will be indexed by total scores on the Distress Tolerance Scale (DTS), which is a 15-item self-report measure that assesses the respondent's perceived ability to withstand distressing or upsetting emotional states. Possible total scores can range from 15 to 75. Higher scores indicate higher distress tolerance. This outcome measure will be examined and compared for both the intervention group and the control group.

次要结局

  • Internalizing Symptoms(Pre-intervention, immediately post-intervention, 3-month follow-up, and 6-month follow-up)

研究者

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

Bonnie Nagel

Principal Investigator

Oregon Health and Science University

研究点 (2)

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