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MIDSHIPS: Multicentre Intervention Designed for Self-Harm using Interpersonal Problem-Solving: protocol for a randomised controlled feasibility study

机译:MIDSHIPS:使用人际解决问题的自我干预设计的多中心干预措施:用于随机对照可行性研究的协议

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Background Around 150,000 people each year attend hospitals in England due to self-harm, many of them more than once. Over 5,000 people die by suicide each year in the UK, a quarter of them having attended hospital in the previous year because of self-harm. Self-harm is a major identifiable risk factor for suicide. People receive variable care at hospital; many are not assessed for their psychological needs and little psychological therapy is offered. Despite its frequent occurrence, we have no clear research evidence about how to reduce the repetition of self-harm. Some people who have self-harmed show less active ways of solving problems, and brief problem-solving therapies are considered the most promising psychological treatments. Methods/Design This is a pragmatic, individually randomised, controlled, feasibility study comparing interpersonal problem-solving therapy plus treatment-as-usual with treatment-as-usual alone, for adults attending a general hospital following self-harm. A total of 60 participants will be randomised equally between the treatment arms, which will be balanced with respect to the type of most recent self-harm event, number of previous self-harm events, gender and age. Feasibility objectives are as follows: a) To establish and field test procedures for implementing the problem-solving intervention; b) To determine the feasibility and best method of participant recruitment and follow up; c) To assess therapeutic delivery; d) To assess the feasibility of obtaining the definitive trial’s primary and secondary outcomes; e) To assess the perceived burden and acceptability of obtaining the trial’s self-reported outcome data; f) To inform the sample size calculation for the definitive trial. Discussion The results of this feasibility study will be used to determine the appropriateness of proceeding to a definitive trial and will allow us to design an achievable trial of interpersonal problem-solving therapy for adults who self-harm. Trial registration Current Controlled Trials ( ISRCTN54036115 )
机译:背景技术由于自我伤害,每年约有15万人在英格兰的医院就诊,其中许多人不止一次。在英国,每年有5,000多人死于自杀,其中四分之一是在去年因自残而入院的。自我伤害是自杀的主要可识别危险因素。人们在医院接受可变护理;许多人的心理需求没有得到评估,很少提供心理治疗。尽管这种情况经常发生,但对于如何减少自残的重复发生,我们尚无明确的研究证据。一些自残的人表现出不太主动的解决问题的方法,而解决问题的简短疗法被认为是最有前途的心理治疗方法。方法/设计这是一项实用的,个体随机,对照,可行性研究,比较了因自残而就诊于综合医院的成年人,其人际间解决问题的方法加常规治疗与常规治疗的比较。总共60名参与者将在治疗组之间平均分配,这将在最近一次自残事件的类型,以前的自残事件的数量,性别和年龄之间取得平衡。可行性目标如下:a)建立并进行现场测试程序以实施解决问题的干预措施; b)确定参与者招募和跟进的可行性和最佳方法; c)评估治疗效果; d)评估获得确定性试验的主要和次要结果的可行性; e)评估获得试验的自我报告结果数据的感知负担和可接受性; f)告知确定试验的样本量计算。讨论该可行性研究的结果将用于确定进行最终试验的适当性,并使我们能够设计出一项针对自残成人的人际问题解决疗法的可行试验。试用注册当前控制的试用(ISRCTN54036115)

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