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A protocol for a multicentre, parallel-group, pragmatic randomised controlled trial to evaluate the NEVERMIND system in preventing and treating depression in patients with severe somatic conditions

机译:用于多中心,并联组,语用随机对照试验的方案,以评估Nevermind系统预防和治疗严重躯体条件的患者抑郁症

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Depressive symptoms are common in individuals suffering from severe somatic conditions. There is a lack of interventions and evidence-based interventions aiming to reduce depressive symptoms in patients with severe somatic conditions. The aim of the NEVERMIND project is to address these issues and provide evidence by testing the NEVERMIND system, designed to reduce and prevent depressive symptoms in comparison to treatment as usual. The NEVERMIND study is a parallel-groups, pragmatic randomised controlled trial to assess the effectiveness of the NEVERMIND system in reducing depressive symptoms among individuals with severe somatic conditions. The NEVERMIND system comprises a smart shirt and a user interface, in the form of a mobile application. The system is a real-time decision support system, aiming to predict the severity and onset of depressive symptoms by modelling the well-being condition of patients based on physiological data, body movement, and the recurrence of social interactions. The study includes 330 patients who have a diagnosis of myocardial infarction, breast cancer, prostate cancer, kidney failure, or lower limb amputation. Participants are randomised in blocks of ten to either the NEVERMIND intervention or treatment as usual as the control group. Clinical interviews and structured questionnaires are administered at baseline, at 12?weeks, and 24?weeks to assess whether the NEVERMIND system is superior to treatment as usual. The endpoint of primary interest is Beck Depression Inventory II (BDI-II) at 12?weeks defined as (i) the severity of depressive symptoms as measured by the BDI-II. Secondary outcomes include prevention of the onset of depressive symptoms, changes in quality of life, perceived stigma, and self-efficacy. There is a lack of evidence-based interventions aiming to reduce and prevent depressive symptoms in patients with severe somatic conditions. If the NEVERMIND system is effective, it will provide healthcare systems with a novel and innovative method to attend to depressive symptoms in patients with severe somatic conditions. DRKS00013391. Registered 23 November 2017.
机译:抑郁症状是患有严重躯体条件的个体中的常见。缺乏干预措施和基于证据的干预措施,旨在减少严重躯体条件严重的患者的抑郁症状。 Nevermind项目的目的是通过测试无需系统来解决这些问题,并提供证据,旨在减少和预防往往与往常进行治疗的抑郁症状。 Nevermind研究是一种平行组,语用随机对照试验,以评估Nevermind系统在减少具有严重躯体条件的个体中抑郁症状的有效性。 NeverMind系统包括智能衬衫和用户界面,以移动应用程序的形式。该系统是一种实时决策支持系统,旨在通过根据生理数据,身体运动和社会互动的复发来建模患者的幸福状况来预测抑郁症状的严重程度和发作。该研究包括330名患者,诊断心肌梗死,乳腺癌,前列腺癌,肾衰竭或下肢截肢。参与者在10个块中随机分配,以便与对照组一样常见的干预或治疗。临床访谈和结构化问卷在12?周和24周内给予基线,以评估Nevermind系统是否优于平常治疗。主要兴趣的终点是Beck抑制库存II(BDI-II)在12?周定义为(i)由BDI-II测量的抑郁症状的严重程度。二次结果包括预防抑郁症状的发病,生活质量的变化,感知耻辱和自我效能。缺乏基于证据的干预措施,旨在减少和预防严重躯体条件患者的抑郁症状。如果富裕系统有效,它​​将提供具有新颖的和创新方法的医疗保健系统,以应对严重躯体条件的患者抑郁症状。 drks00013391。注册2017年11月23日。

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