ACTRN12613001270707已完成未知
Randomised controlled trial to measure the efficacy of a metacognitive based treatment for adults with prolonged grief
Dr Moira O'Connor0 个研究点目标入组 50 人开始时间: 2013年11月18日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 50
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
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •Participant inclusion criteria will be: 1) provision of written informed consent; 2) intense symptoms of grief or PGD (as determined by PG-13) 6 months post the loss of a significant other; 3) if taking medication (namely, antidepressants or other mood stabilisers), the medication must be stable for one month prior to baseline assessment. Participants need to remain on the same dosage and medication throughout the treatment period including follow-up.
排除标准
- •Participant exclusion criteria will be: 1) a high suicidal risk as measured by the suicidality section of the MINI (Sheehan et al., 1997); 2) participants currently undergoing other psychological treatment; and 3) a pre-existing psychiatric (excluding: anxiety & depression) or neurological history, according to the DSMIV-TR diagnostic criteria, as measured by the SCID. Participants that do not meet the inclusion criteria/or meet the exclusion criteria will be excluded from the study and will be provided referral information (such as Lifeline or Crisis Care), or for those identified with high suicidality we will consult with their psychiatrist or local general practitioner.
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