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首页> 外文期刊>Trials >Protocol for a randomised controlled trial of a school based cognitive behaviour therapy (CBT) intervention to prevent depression in high risk adolescents (PROMISE)
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Protocol for a randomised controlled trial of a school based cognitive behaviour therapy (CBT) intervention to prevent depression in high risk adolescents (PROMISE)

机译:基于学校的认知行为疗法(CBT)干预以预防高危青少年抑郁症(PROMISE)的随机对照试验协议

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摘要

Background Depression in adolescents is a significant problem that impairs everyday functioning and increases the risk of severe mental health disorders in adulthood. Relatively few adolescents with depression are identified and referred for treatment indicating the need to investigate alternative preventive approaches. Study Design A pragmatic cluster randomised controlled trial evaluating the effectiveness of a school based prevention programme on symptoms of depression in "high risk" adolescents (aged 12-16). The unit of allocation is year groups (n = 28) which are assigned to one of three conditions: an active intervention based upon cognitive behaviour therapy, attention control or treatment as usual. Assessments will be undertaken at screening, baseline, 6 months and 12 months. The primary outcome measure is change on the Short Mood and Feeling Questionnaire at 12 months. Secondary outcome measures will assess changes in negative thoughts, self esteem, anxiety, school connectedness, peer attachment, alcohol and substance misuse, bullying and self harm. Discussion As of August 2010, all 28 year groups (n = 5023) had been recruited and the assigned interventions delivered. Final 12 month assessments are scheduled to be completed by March 2011. Trial Registration ISRCTN19083628
机译:背景技术青少年的抑郁症是一个严重的问题,它损害了日常功能,并增加了成年后出现严重精神健康障碍的风险。识别出抑郁症的青少年相对较少,并转诊接受治疗,表明需要研究其他预防方法。研究设计一项实用的整群随机对照试验,评估以学校为基础的预防计划对“高风险”青少年(12-16岁)的抑郁症状的有效性。分配的单位是年组(n = 28),它们被分配为以下三种情况之一:基于认知行为疗法的积极干预,注意力控制或照常治疗。评估将在筛选,基线,6个月和12个月时进行。主要结局指标是在12个月时改变“短期情绪和情感问卷”。次要结果测量将评估负面思想,自尊,焦虑,学校联系,同伴依恋,酗酒和滥用药物,欺凌和自我伤害的变化。讨论截至2010年8月,已经招募了所有28年组(n = 5023),并交付了指定的干预措施。最终的12个月评估计划于2011年3月完成。试用注册ISRCTN19083628

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