跳至主要内容
临床试验/NCT04903431
NCT04903431已完成不适用

Assessing the Effectiveness of Self- and Clinician-administered Crisis Response Planning for Suicide Risk

Ohio State University1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2021年12月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
75
试验地点
1
主要终点
Change in Suicide Visual Analog Scale scores from the previous daily assessment

研究概览

简要总结

The aim of the current project is to compare the use and preliminary effectiveness of a self-administered version of the Crisis Response Plan (CRP) in decreasing suicidal/death ideation and distress and increasing positive affect when compared to a clinician-administered version of the protocol in a sample of 150 military Veterans experiencing current death or suicidal ideation.

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
None

入排标准

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

入选标准

  • •18 years of age or older
  • •US military veteran
  • •death or suicidal ideation/suicide attempt within the past month

排除标准

  • •non-Veteran status
  • •acute intoxication or active psychosis precluding provision of informed consent
  • •inability to communicate and comprehend English
  • •residence outside the United States
  • •lack of past-month death/suicide ideation or attempt
  • •lack of device connected to webcam or internet

研究组 & 干预措施

Clinician-administered Crisis Response Plan

Active Comparator

Clinicians will administer the Crisis Response Plan to 75 military veterans.

干预措施: Crisis Response Planning for Suicide Risk (Behavioral)

Self-administered Crisis Response Plan

Experimental

Participants will complete a self-guided version of the Crisis Response plan online.

干预措施: Crisis Response Planning for Suicide Risk (Behavioral)

结局指标

主要结局

Change in Suicide Visual Analog Scale scores from the previous daily assessment

时间窗: Administered daily for eight consecutive days

The Suicide Visual Analog Scale The S-VAS assesses "urge to kill myself" using a horizontal line with anchors on the left reflecting "none" (score: 0) and on the right reflecting "extreme" (score: 100). The S-VAS is initially presented with the indicator on the "none" position, and non-movement of the indicator is followed by a prompt to remind the participant to move the indicator, if relevant, to ensure response accuracy. Higher scores are indicative of greater severity

次要结局

  • Change in Patient Health Questionnaire - 2 scores from the previous daily assessment(Administered daily for eight consecutive days)
  • Change in Positive and Negative Affect Schedule - Short Form scores from the previous daily assessment(Administered daily for eight consecutive days)
  • Change in Crisis Response Plan Use from the previous daily assessment(Administered daily for eight consecutive days)

研究者

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

Lauren Khazem

Principal Investigator

Ohio State University

研究点 (1)

Loading locations...

相似试验

Assessing the Effectiveness of Self- and... | 临床试验