Brief education supported psychological treatment for adolescent borderline personality disorder: the BEST feasibility RCT

Jon Wilson, Brioney Gee, N. Martin, S. Maxwell, J. Murdoch, Tim Clarke, A. Clark, D. Turner, C. Notley, Thando Katangwe, P. Jones, P. Fonagy
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Therefore, there is an urgent need for accessible interventions to facilitate early intervention for adolescents with borderline personality disorder symptoms.\n \n \n \n The first objective was to adapt a brief psychological treatment for adolescent borderline personality disorder that had previously been delivered within secondary mental health services for co-delivery within schools and colleges. The second objective was to assess the feasibility of evaluating the clinical effectiveness and cost-effectiveness of this intervention in a future randomised controlled trial.\n \n \n \n We first conducted a rapid evidence synthesis of barriers to and facilitators of the implementation of indicated mental health interventions for adolescents within educational settings and piloted the prototype intervention with three schools/colleges. 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The findings provide support for continuing this programme of research and would inform the design of a future trial.\n \n \n \n This trial is registered as ISRCTN16862589.\n \n \n \n This project was funded by the National Institute for Health and Care Research (NIHR) Health and Social Care Delivery Research programme and will be published in full in Health and Social Care Delivery Research; Vol. 10, No. 37. 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Abstract

Borderline personality disorder is a severe mental health condition characterised by a pattern of emotional instability, interpersonal dysfunction, disturbed self-image and impulsive behaviour, including self-harm. Symptoms of borderline personality disorder typically emerge during adolescence. Although there is compelling evidence in support of early intervention for borderline personality disorder, current evidence-based interventions are resource intensive, with the result that few young people access timely treatment. Therefore, there is an urgent need for accessible interventions to facilitate early intervention for adolescents with borderline personality disorder symptoms. The first objective was to adapt a brief psychological treatment for adolescent borderline personality disorder that had previously been delivered within secondary mental health services for co-delivery within schools and colleges. The second objective was to assess the feasibility of evaluating the clinical effectiveness and cost-effectiveness of this intervention in a future randomised controlled trial. We first conducted a rapid evidence synthesis of barriers to and facilitators of the implementation of indicated mental health interventions for adolescents within educational settings and piloted the prototype intervention with three schools/colleges. Based on the findings of the evidence synthesis and pilot, we refined the intervention and study procedures in preparation for a feasibility randomised controlled trial. The feasibility randomised controlled trial involved 12 schools and colleges, whose pastoral staff members received training to deliver the intervention alongside a mental health practitioner. Participants were randomised in a 1 : 1 ratio to receive either the BEST (Brief Education Supported Treatment) intervention plus treatment as usual or treatment as usual alone. Participants were assessed pre randomisation (baseline) and at 12 and 24 weeks post randomisation. Mixed-methods process data were collected to understand how the intervention was implemented, to assess acceptability and to monitor contamination of the control arm. Young people eligible to participate were aged 13–18 years, reported symptoms of borderline personality disorder above an established threshold and had a history of repeated self-harm. The intervention was refined based on findings of the rapid evidence synthesis, which included 50 studies, feedback from staff participants in the pilot and analysis of session recordings. In the feasibility randomised controlled trial, we randomised 32 participants prior to the premature closure of recruitment. The rate of recruitment was slower than anticipated but would probably have narrowly surpassed our progression criterion over the full recruitment window. Participant retention was high (89.5% at 12 weeks and 73.7% at 24 weeks) and the performance of the proposed outcome measures was satisfactory. We did not find any evidence that participants allocated to the treatment-as-usual arm received the BEST intervention or its components. Fidelity of intervention delivery was high (93.5% of recordings rated as adherent) and the intervention was viewed as offering benefits for individual participants, practitioners involved in co-delivery and the wider school/college. The feasibility randomised controlled trial was disrupted by the closure of schools and colleges in response to the COVID-19 pandemic. This reduced the window for participant recruitment and limited the data that could be collected. The refined BEST intervention was able to be delivered successfully within schools and colleges and was found to be acceptable to staff and young people. The findings provide support for continuing this programme of research and would inform the design of a future trial. This trial is registered as ISRCTN16862589. This project was funded by the National Institute for Health and Care Research (NIHR) Health and Social Care Delivery Research programme and will be published in full in Health and Social Care Delivery Research; Vol. 10, No. 37. See the NIHR Journals Library website for further project information.
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青少年边缘型人格障碍的简短教育支持心理治疗:最佳可行性随机对照试验
边缘型人格障碍是一种严重的心理健康状况,其特征是情绪不稳定、人际功能障碍、自我形象紊乱和冲动行为,包括自残。边缘型人格障碍的症状通常出现在青春期。尽管有令人信服的证据支持对边缘型人格障碍进行早期干预,但目前的循证干预是资源密集型的,因此很少有年轻人能得到及时的治疗。因此,迫切需要可获得的干预措施,以促进对有边缘型人格障碍症状的青少年的早期干预。第一个目标是将以前在中等心理健康服务机构提供的青少年边缘型人格障碍的简短心理治疗改为在学校和大学内共同提供。第二个目标是在未来的随机对照试验中评估这种干预措施的临床有效性和成本效益的可行性。我们首先对在教育环境中实施针对青少年的心理健康干预措施的障碍和促进因素进行了快速证据综合,并在三所学校/学院试行了原型干预措施。根据证据综合和试点的结果,我们完善了干预和研究程序,为可行性随机对照试验做准备。这项可行性随机对照试验涉及12所学校和学院,这些学校和学院的教职员与一名心理健康从业者一起接受了干预培训。参与者被随机分为1组 : 接受BEST(短期教育支持治疗)干预加照常治疗或单独照常治疗的比例为1。随机分组前(基线)以及随机分组后12周和24周对参与者进行评估。收集混合方法过程数据,以了解干预措施是如何实施的,评估可接受性,并监测控制臂的污染情况。有资格参加的年轻人年龄在13-18岁之间,报告有超过既定阈值的边缘型人格障碍症状,并有多次自残史。干预措施是根据快速证据综合的结果进行改进的,其中包括50项研究、试点工作人员的反馈以及对会议记录的分析。在可行性随机对照试验中,我们在招募提前结束前对32名参与者进行了随机分组。招聘速度比预期的要慢,但在整个招聘窗口内可能会勉强超过我们的晋升标准。参与者的保留率很高(12周时为89.5%,24周时为73.7%),所提出的结果指标的表现令人满意。我们没有发现任何证据表明,被分配到照常治疗组的参与者接受了最佳干预或其组成部分。干预实施的保真度很高(93.5%的记录被评为依从性),干预被视为为为个人参与者、参与共同实施的从业者和更广泛的学校/学院提供了好处。可行性随机对照试验因新冠肺炎疫情导致学校和大学关闭而中断。这减少了参与者招募的窗口,并限制了可以收集的数据。经过改进的BEST干预措施能够在学校和学院内成功实施,并被发现为工作人员和年轻人所接受。研究结果为继续这一研究方案提供了支持,并将为未来试验的设计提供信息。该试验注册为ISRCTN16862589。该项目由国家卫生与护理研究所(NIHR)卫生与社会护理提供研究计划资助,并将在《卫生与社会保健提供研究》上全文发表;第10卷,第37期。有关更多项目信息,请访问NIHR期刊图书馆网站。
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