ACTRN12615000438550招募中未知
Randomised Controlled Trial of Enhanced Monitoring or Treatment As Usual for Adults to Treat PosttraumaticStress Disorder Following Traumatic Injury
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 入组人数
- 200
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
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •Adults survivors of traumatic injury who are admitted to hospital following injury
排除标准
- •1.Patients with a moderate to severe traumatic brain injury as defined by
- •a.A GCS score < 12 – as per the Emergency Department (ED) assessment
- •b.Ongoing Post Traumatic Amnesia (PTA) testing > 72 hours
- •c.NOTE: Refer to MTBI decision making tree (appendix) if there are other reasons for altered GCS or PTA score (e.g., intubation of patient)
- •2.Patients unable to understand the study procedures, consent, or willingly participate in the study protocol
- •3.Patients with moderate dementia or severe cognitive impairment
- •4.Patients with severe suicidal ideation (i.e., if the injury was the result of a suicide attempt, as defined by the electronic medical records at Royal North Shore Hospital).
- •5.Patients with psychosis (as defined by the electronic medical records at Royal North Shore Hospital).
研究者
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