跳至主要内容
临床试验/ACTRN12620000053921
ACTRN12620000053921撤回未知

An optimisation trial of an SMS-based, brief intervention after hospitalisation for self-harm, a suicide attempt, or suicidal ideation, targeting proximal risk factors for self-harm and suicide.

niversity of New South Wales0 个研究点目标入组 250 人开始时间: 2020年1月23日最近更新:
适应症

试验速览

阶段
未知
状态
撤回
入组人数
250

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
16 Years 至 65 Years(—)
性别
All

入选标准

  • Individuals are eligible to join the study if they:
  • - Are currently aged between 16-65 years old.
  • - Presented at a hospital within the last 7 days for self-harm, suicidal ideation, or a suicide attempt.
  • - Have a smart phone with an Australian phone number.
  • - Provide their consent to participate, including consent to allow the research team to access their hospital medical records for 12 months prior to enrolment and 12 months post enrolment in the study.

排除标准

  • Individuals are excluded from participation if they:
  • - Are not currently aged between 16 and 65 years old.
  • - Presented to the hospital with psychotic symptoms.
  • - Are not English literate.

研究者

相似试验