跳至主要内容
临床试验/NCT01300169
NCT01300169已完成不适用

A Randomized Clinical Trial of the Collaborative Assessment and Management of Suicidality Versus Enhanced Care as Usual for Suicidal Soldiers

The Catholic University of America0 个研究点目标入组 150 人开始时间: 2011年3月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
150
主要终点
Scale for Suicidal Ideation

研究概览

简要总结

This is a randomized controlled trial comparing the use of new clinical intervention (the "Collaborative Assessment and Management of Suicidality--CAMS") versus enhanced care as usual for suicidal Soldiers who are seen at outpatient mental health clinics at Ft. Stewart GA.

详细描述

This is a randomized controlled clinical trial of 148 suicidal active-duty US Army Soldiers. Participants were randomized to on-site providers who were trained in the Collaborative Assessment and Management of Suicidality (CAMS) vs. providers doing their own routine care--referred to as Enhanced Care as Usual (E-CAU) within an outpatient military treatment center. The CAMS Rating Scale (CRS) was used to reliably verify fidelity between treatment conditions and the adherence by CAMS providers to the model. Participants received informed consent to be randomly assigned to treatment arm and were ask to complete study assessments at baseline, 3 months, 6 months, and 12 months after the start of treatment. Recruitment is complete and all study assessments were completed as of March 2016. The study is in a second year of no cost extension; outcome data analyses and moderator analyses are currently underway to develop manuscripts for submission to peer-review scientific journals.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

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

  • Active duty Army personnel at FSGA
  • Significant suicidal ideation
  • Soldier is appropriate under FSGA policies
  • Consent at baseline and follow up
  • Consent to randomization and being digitally recorded

排除标准

  • Significant psychosis, cognitive or physical impairment to not give consent
  • Judicially ordered treatments

结局指标

主要结局

Scale for Suicidal Ideation

时间窗: Baseline, post-treatment, 1, 3, 6, 12 months

Industry standard for self-report suicidal ideation

次要结局

  • Overall symptom distress(Baseline, post treatment, 1, 3, 6, 12 months)

研究者

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

David A. Jobes, Ph.D.

Professor of Psychology

The Catholic University of America

相似试验