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首页> 外文期刊>Trials >Glioma patients in outpatient care—optimization of psychosocial care in neuro-oncological patients (GLIOPT): Protocol for a cluster randomized controlled trial
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Glioma patients in outpatient care—optimization of psychosocial care in neuro-oncological patients (GLIOPT): Protocol for a cluster randomized controlled trial

机译:神经肿瘤患者在神经肿瘤患者(GLIOPT)中的门诊护理患者(GLIOPT):群体随机对照试验的议定书

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BACKGROUND:Patients with high-grade gliomas (HGG) often suffer from high distress and require psychosocial support. However, due to neurological and neurocognitive deficits, adequate assessment of distress and support needs remains challenging in clinical practice. The objective of the present study is to investigate whether a systematic implementation of signaling questions into the routine outpatient consultation will be helpful to bridge this gap.METHODS/DESIGN:This is a multicenter cluster randomized study with two arms. Randomization is done on a cluster level with 13 hospitals providing regular neuro-oncological outpatient services conducted by neurologists and/or neurosurgeons. The intervention will include an assessment of psychosocial distress of patients in doctor-patient conversation compared to assessment of psychosocial distress via questionnaire (control, standard of care). In total, 616 HGG patients will be enrolled. The outcome will be the number of HGG patients with increased psychosocial distress who receive professional support from psychosocial services. Secondary endpoints are inter alia number of patients reporting psychosocial distress and unmet needs detected correctly by the respective method; quality of life; psychological well-being and burden of the patients before and after doctor-patient consultation; as well as the length of the doctor-patient consultation.DISCUSSION:Patients with HGG are confronted with an oncological diagnosis and at the same time with high symptom burden. This often leads to distress, which is not always adequately recognized and treated. So far, only a limited number of adequate instruments are available to assess HGG patient's distress. Yet, an adequate care and support network might facilitate the course of the disease and tumor therapies for patients. Our hypothesis is that an assessment conducted directly by attending doctors and in which the doctors talk to patients with HGG will be more effective than an assessment via a questionnaire, leading to better identifying patients in need of support. This may lead to an improvement of health care in these patients. Further, this method might be implemented also in other brain tumor patients (e.g., patients with brain metastases).TRIAL REGISTRATION:German Clinical Trials Register, DRKS00018079. Registered on 3rd September 2019.
机译:背景:高级胶质瘤(HGG)的患者经常遭受高痛苦,需要心理社会支持。然而,由于神经和神经认知缺陷,对临床实践的充分评估痛苦和支持需求仍然具有挑战性。本研究的目的是调查信息传导问题是否进入常规门诊咨询的系统执行情况将有助于弥补这一差距。方法/设计:这是一个用两臂的多中心群集随机研究。随机化是在集群级别完成的,其中13家医院提供神经科学家和/或神经外科医院进行的常规神经肿瘤门诊服务。与通过调查问卷评估(控制,护理标准)评估心理社会痛苦的评估,干预将包括评估医生谈话中的患者的心理社会困扰。总共有616名HGG患者注册。结果将成为从社会社会服务获得专业支持的心理社会危机增加的HGG患者的数量。次要终点尤其是通过各个方法正确检测到的心理社会遇险和未满足的患者的患者的数量;生活质量;医患咨询前后患者的心理健康和负担;除了医生咨询的长度。探讨:HGG的患者面临着肿瘤诊断,同时具有高症状负担。这通常会导致痛苦,这并不总是充分认可和治疗。到目前为止,只有有限数量的足够的仪器可以评估HGG病人的痛苦。然而,充分的护理和支持网络可能有助于患者疾病和肿瘤疗法的过程。我们的假设是通过参加医生直接进行的评估,其中医生与HGG患者谈论比通过调查问卷的评估更有效,从而更好地识别需要支持的患者。这可能会导致这些患者的医疗保健改善。此外,该方法也可以在其他脑肿瘤患者中实现(例如,脑转移患者).Trial注册:德国临床试验登记,DRKS00018079。 2019年9月3日注册。

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