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首页> 外文期刊>Trials >The second Symptom Management Research Trial in Oncology (SMaRT Oncology-2): a randomised trial to determine the effectiveness and cost-effectiveness of adding a complex intervention for major depressive disorder to usual care for cancer patients
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The second Symptom Management Research Trial in Oncology (SMaRT Oncology-2): a randomised trial to determine the effectiveness and cost-effectiveness of adding a complex intervention for major depressive disorder to usual care for cancer patients

机译:肿瘤学第二次症状管理研究试验(SMaRT Oncology-2):一项随机试验,以确定在癌症患者的常规治疗中增加对重度抑郁症的复杂干预措施的有效性和成本效益

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Background Depression Care for People with Cancer is a complex intervention delivered by specially trained cancer nurses, under the supervision of a psychiatrist. It is given as a supplement to the usual care for depression, which patients receive from their general practitioner and cancer service. In a 'proof of concept' trial (Symptom Management Research Trials in Oncology-1) Depression Care for People with Cancer improved depression more than usual care alone. The second Symptom Management Research Trial in Oncology (SMaRT Oncology-2 Trial) will test its effectiveness and cost-effectiveness in a 'real world' setting. Design A two arm parallel group multi-centre randomised controlled trial. Trial Procedures 500 patients will be recruited through established systematic Symptom Monitoring Services, which screen patients for depression. Patients will have: a diagnosis of cancer (of various types); an estimated life expectancy of twelve months or more and a diagnosis of Major Depressive Disorder. Patients will be randomised to usual care or usual care plus Depression Care for People with Cancer. Randomisation will be carried out by telephoning a secure computerised central randomisation system or by using a secure web interface. The primary outcome measure is 'treatment response' measured at 24 week outcome data collection. 'Treatment response' will be defined as a reduction of 50% or more in the patient's baseline depression score, measured using the 20-item Symptom Checklist (SCL-20D). Secondary outcomes include remission of major depressive disorder, depression severity and patients' self-rated improvement of depression. Trial Registration Current controlled trials ISRCTN40568538 Trial Hypotheses (1) Depression Care for People with Cancer as a supplement to usual care will be more effective than usual care alone in achieving a 50% reduction in baseline SCL-20D score at 24 weeks. (2) Depression Care for People with Cancer as a supplement to usual care will cost more than usual care alone but will be more cost effective in achieving improvements in patients' depression and quality of life.
机译:背景癌症患者的抑郁症护理是由受过专门培训的癌症护士在精神科医生的监督下提供的复杂干预措施。它是对常规抑郁治疗的补充,患者可以从全科医生和癌症服务部门获得该治疗。在一项“概念验证”试验(肿瘤学-1中的症状管理研究试验)中,针对癌症患者的抑郁症治疗比单独的常规治疗更能改善抑郁症。第二项肿瘤症状管理研究试验(SMaRT Oncology-2试验)将在“现实世界”环境中测试其有效性和成本效益。设计两臂平行组多中心随机对照试验。试验程序将通过建立的系统症状监测服务招募500名患者,以筛查患者是否患有抑郁症。患者将具有:(各种类型)癌症的诊断;预期寿命为十二个月或更长时间,并诊断为重度抑郁症。患者将被随机分配至癌症患者的常规治疗或常规治疗加抑郁症治疗。可以通过给安全的计算机化中央随机系统打电话或使用安全的网络界面来进行随机化。主要结局指标是收集24周结局数据时测得的“治疗反应”。 “治疗反应”将定义为使用20项症状清单(SCL-20D)测量的患者基线抑郁评分降低50%或更多。次要结果包括重度抑郁症的缓解,抑郁症的严重程度和患者对抑郁症的自我评价。试验注册当前的对照试验ISRCTN40568538试验假设(1)癌症患者的抑郁症治疗作为常规治疗的补充措施,比单独的常规治疗更有效,可以在24周时将基线SCL-20D评分降低50%。 (2)癌症患者的抑郁症治疗作为常规治疗的补充,其费用将比仅常规治疗高,但在改善患者抑郁和生活质量方面将更具成本效益。

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