Freeman Daniel, Waite Felicity, Emsley Richard, Kingdon David, Davies Linda, Fitzpatrick Ray, Dunn Graham
Department of Psychiatry, University of Oxford, Warneford Hospital, Oxford, OX3 7JX, UK.
Centre for Biostatistics, Institute of Population Health, Manchester University, Manchester Academic Health Centre, Manchester, UK.
Trials. 2016 Mar 11;17(1):134. doi: 10.1186/s13063-016-1245-0.
Persecutory delusions (strong unfounded fears that others intend harm to the person) occur in more than 70 % of the patients diagnosed with schizophrenia. This major psychotic experience is a key clinical target, for which substantial improvement in treatment is needed. Our aim is to use advances in theoretical understanding to develop a much more efficacious treatment that leads to recovery in at least 50 % of people with persistent persecutory delusions. Our cognitive conceptualisation is that persecutory delusions are threat beliefs, developed in the context of genetic and environmental risk, maintained by a number of psychological processes including excessive worry, low self-confidence, intolerance of anxious affect and other internal anomalous experiences, reasoning biases, and safety-seeking strategies. The clinical implication is that safety has to be relearned, by entering the feared situations after reduction of the influence of the maintenance factors. We have been individually evaluating modules targeting causal factors. These will now be tested together as a full treatment, called The Feeling Safe Programme. The treatment is modular, personalised, and includes patient preference. We will test whether the new treatment leads to greater recovery in persistent persecutory delusions, psychological well-being, and activity levels compared to befriending (that is, controlling for therapist attention).
METHODS/DESIGN: The Feeling Safe Study is a parallel group randomised controlled trial for 150 patients who have persecutory delusions despite previous treatment in mental health services. Patients will be randomised (1:1 ratio) to The Feeling Safe Programme or befriending (both provided in 20 sessions over 6 months). Standard care will continue as usual. Online randomisation will use a permuted blocks algorithm, with randomly varying block size, stratified by therapist. Assessments, by a rater blind to allocation, will be conducted at 0, 6 (post treatment), and 12 months. The primary outcome is the level of delusional conviction at 6 months. Secondary outcomes include levels of psychological well-being, suicidal ideation, and activity. All main analyses will be intention-to-treat. The trial is funded by the NHS National Institute for Health Research.
The Feeling Safe study will provide a Phase II evaluation of a new targeted translational psychological treatment for persecutory delusions.
Current Controlled Trials ISRCTN18705064 (registered 11 November 2015).
被害妄想(毫无根据的强烈恐惧,认为他人意图伤害自己)在超过70%被诊断为精神分裂症的患者中出现。这种主要的精神病性体验是一个关键的临床治疗靶点,急需在治疗上取得实质性进展。我们的目标是利用理论认识的进步,开发一种更有效的治疗方法,使至少50%患有持续性被害妄想的患者康复。我们的认知概念是,被害妄想是在遗传和环境风险背景下形成的威胁信念,由包括过度担忧、缺乏自信、无法忍受焦虑情绪和其他内部异常体验、推理偏差以及寻求安全策略等多种心理过程维持。临床意义在于,在减少维持因素的影响后,通过进入恐惧情境来重新学习安全感。我们一直在单独评估针对因果因素的模块。现在这些模块将作为一种完整的治疗方法一起进行测试,称为“安全感计划”。该治疗方法具有模块化、个性化特点,并考虑患者偏好。我们将测试与交友疗法(即控制治疗师的关注)相比,这种新治疗方法是否能使持续性被害妄想患者在康复、心理健康和活动水平方面有更大改善。
方法/设计:“安全感研究”是一项平行组随机对照试验,针对150名尽管之前在精神卫生服务机构接受过治疗但仍患有被害妄想的患者。患者将按1:1的比例随机分配到“安全感计划”组或交友疗法组(两者均在6个月内进行20次治疗)。标准护理将照常进行。在线随机分组将使用置换块算法,块大小随机变化,并按治疗师进行分层。由对分组不知情的评估者在0、6个月(治疗后)和12个月进行评估。主要结局指标是6个月时的妄想坚信程度。次要结局指标包括心理健康水平、自杀意念和活动情况。所有主要分析将采用意向性分析。该试验由英国国家医疗服务体系(NHS)国家卫生研究院资助。
“安全感研究”将为一种针对被害妄想的新型靶向转化心理治疗提供II期评估。
当前受控试验ISRCTN18705064(2015年11月11日注册)