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Optimizing psychotherapy dosage for comorbid depression and personality disorders (PsyDos): a?pragmatic randomized factorial trial using schema therapy and short-term psychodynamic psychotherapy

机译:针对合并症抑郁症和人格障碍(PsyDos)优化心理治疗剂量:使用方案治疗和短期心理动力心理治疗的实用性随机析因试验

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Patients with comorbid depression and personality disorders suffer from a heavy disease burden while tailored treatment options are limited, accounting for a high psychological and economic burden. Little is known about the effect of treatment dosage and type of psychotherapy for this specific co-morbid patient population, in terms of treatment-effect and cost-effectiveness. This study aims to compare treatment outcome of 25 versus 50 individual therapy sessions in a year. We expect the 50-session condition to be more effective in treating depression and maintaining the effect. Secondary objectives will be addressed in order to find therapy-specific and non-specific mechanisms of change. In a mono-center pragmatic randomized controlled trial with a 2?×?2 factorial design, 200 patients with a depressive disorder and personality disorder(s) will be included. Patients will be recruited from a Dutch mental health care institute for personality disorders. They will be randomized over therapy dosage (25 vs 50 sessions in a year) and type of therapy (schema therapy vs short-term psychodynamic supportive psychotherapy). The primary clinical outcome measure will be depression severity and remission. Changes in personality functioning and quality of life will be investigated as secondary outcomes. A priori postulated effect moderators and mediators will be collected as well. All patients are assessed at baseline and at 1, 2, 3, 6, 9–12?months (end of therapy) and at follow up (6 and 12?months after end of treatment). Alongside the trial, an economic evaluation will be conducted. Costs will be collected from a societal perspective. This trial will be the first to compare two psychotherapy dosages in patients with both depression and personality disorders. Insight in the effect of treatment dosage for this patient group will contribute to both higher treatment effectiveness and lower costs. In addition, this study will contribute to the limited evidence base on treating patients with both depression and personality disorders. Understanding the processes that account for the therapeutic changes could help to gain insight in what works for whom. This trial has been registered on July 20th 2016, Netherlands Trial Register, part of the Dutch Cochrane Centre ( NTR5941 ).
机译:患有合并症的抑郁症和人格障碍的患者承受着沉重的疾病负担,而量身定制的治疗选择则受到限制,这在心理和经济上造成了沉重负担。就治疗效果和成本效益而言,对于这种特定的合并病患者群体的治疗剂量和心理疗法类型的影响知之甚少。这项研究旨在比较一年中25次和50次单独治疗的治疗结果。我们希望50个疗程的病情能够更有效地治疗抑郁症并保持疗效。次要目标将得到解决,以便找到治疗特异性和非特异性的变化机制。在一项采用2××2因子析因设计的单中心实用性随机对照试验中,将包括200名患有抑郁症和人格障碍的患者。患者将从荷兰精神卫生保健机构招募人格障碍患者。他们将根据治疗剂量(一年25次与50次疗程)和治疗类型(模式治疗与短期心理动力支持性心理治疗)进行随机分组。主要的临床结局指标是抑郁症的严重程度和缓解。人格功能和生活质量的变化将作为次要结果进行调查。还将收集先验假定的效果主持人和调解人。在基线,1、2、3、6、9-12月(治疗结束)和随访(治疗结束后6和12月)对所有患者进行评估。除审判外,还将进行经济评估。将从社会角度收集费用。该试验将是第一个比较抑郁症和人格障碍患者两种心理治疗剂量的试验。对该患者组的治疗剂量效果的了解将有助于提高治疗效果和降低成本。此外,这项研究将为治疗抑郁症和人格障碍患者提供有限的证据。了解导致治疗性变化的过程可能有助于洞察什么对谁有效。该试验已于2016年7月20日在荷兰科克伦中心(NTR5941)的一部分荷兰注册登记处进行注册。

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