跳至主要内容
临床试验/NCT04129866
NCT04129866Unknown不适用

Mobile Interpretation Bias Modification Clinical Trial

University of Southern Mississippi2 个研究点 分布在 1 个国家目标入组 114 人开始时间: 2019年12月15日最近更新:
适应症

试验速览

阶段
不适用
入组人数
114
试验地点
2
主要终点
Anxiety Sensitivity Index-3 Cognitive Concerns Subscale

研究概览

简要总结

The Mobile-Interpretation Bias Modification clinical trial aims to examine the efficacy of a brief mobile phone delivered interpretation bias modification to reduce anxiety sensitivity cognitive concerns and suicidal ideation in National Guard Personnel. The investigators propose a randomized controlled trial testing the efficacy, acceptability, and usability of M-IBM with a sample of 114 National Guardsmen with current suicidal ideation and elevated anxiety sensitivity cognitive concerns. Participants will complete assessments, receive assistance on installing M- IBM on their phone, complete an M-IBM intervention session, and complete post-intervention assessments. Baseline measures of psychopathology, and usability/acceptability of M-IBM will be obtained during the initial session. In addition, 1-month, and 3-month follow-ups would be scheduled to examine changes in psychopathology. The investigators hypothesize that those randomized to M-IBM will experience reductions in anxiety sensitivity cognitive concerns, suicidal ideation. In addition participants will find M-IBM acceptable and easy to use.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Elevated ASCC (>2) and include only Guard members who also have current SI (> 0) .
  • Ownership of a smartphone

排除标准

  • those determined by military or study personnel to be actively psychotic, manic, or imminently suicidal and in need of emergency services

结局指标

主要结局

Anxiety Sensitivity Index-3 Cognitive Concerns Subscale

时间窗: 3 months post intervention

Range 0 - 24, Higher Scores mean more pathology

The Self-Injurious Thoughts and Behaviors Interview

时间窗: 3 months post intervention

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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