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.
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
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