首页> 美国卫生研究院文献>Neuro-Oncology >HOUT-15. BRAIN TUMOR PATIENT AND CAREGIVER SURVEY ON CLINICAL TRIALS: IDENTIFYING ATTITUDES AND BARRIERS TO PATIENT PARTICIPATION
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HOUT-15. BRAIN TUMOR PATIENT AND CAREGIVER SURVEY ON CLINICAL TRIALS: IDENTIFYING ATTITUDES AND BARRIERS TO PATIENT PARTICIPATION

机译:HOUT-15。临床试验中的脑部肿瘤患者和行颅骨检查:确定患者参与的态度和障碍

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摘要

The National Brain Tumor Society conducted an online survey to determine if, when, and how information about clinical trials is provided to brain tumor patients and their caregivers, as well as to understand the perceptions and barriers around clinical trial participation. Questions were tailored for either patient or caregiver respondents, each with further stratification based on whether the patient was newly diagnosed/first occurrence or diagnosed with a recurrent primary brain tumor. There was a total of 1,463 respondents, of which 54% were caregivers with 73% of patients having/had first occurrence brain tumors. Among the different brain tumor types represented in the sample, glioblastoma made up the majority (36%), followed by meningioma (18%), astrocytoma (17%), oligodendroglioma (11%) and a mix of other types (29%), with 2% of respondents unsure of their diagnosis. The survey was open to brain tumor metastases patients, but an insufficient number of respondents met the true definition of “metastatic” preventing their inclusion in the overall analysis. When asked if patients had been informed about clinical trials by their medical team, 42% reported being informed, while 36% stated they had never discussed clinical trials with their provider. When patients were informed about clinical trials, only 24% were informed at the time of their diagnosis. Of the total sample, 21% of patients had participated in a clinical trial. When asked why patients had not participated in clinical trials, the top reasons given were: 1) the patient’s provider did not recommend participating in the trial, 2) the patient did not qualify for clinical trial(s), and 3) the patient and caregiver did not know where to find a clinical trial. The survey results underscore the need for better resources and decision support that will enable patients to be more fully informed about the importance of their participation in appropriately matched clinical trials.
机译:美国国家脑肿瘤学会进行了一项在线调查,以确定是否,何时以及如何向脑肿瘤患者及其护理人员提供有关临床试验的信息,以及了解对参与临床试验的看法和障碍。针对患者或护理人员的问题量身定制了问题,每个问题都根据患者是新诊断/首次出现还是被诊断患有复发性原发性脑肿瘤而进一步分层。共有1,463名受访者,其中54%为看护人,其中73%的患者患有/曾经患有脑肿瘤。在样本所代表的不同脑肿瘤类型中,胶质母细胞瘤占大多数(36%),其次是脑膜瘤(18%),星形细胞瘤(17%),少突胶质细胞瘤(11%)和其他类型的混合物(29%) ,其中2%的受访者不确定其诊断。该调查对脑肿瘤转移患者开放,但数量不足的受访者符合“转移性”的真正定义,因而无法将其纳入整体分析。当被问及患者是否已被其医疗团队告知有关临床试验的信息时,有42%的患者表示已知情,而36%的患者表示他们从未与提供者讨论过临床试验。当告知患者有关临床试验的信息时,在诊断时仅告知了24%。在全部样本中,有21%的患者参加了临床试验。当被问及为什么患者不参加临床试验时,给出的主要理由是:1)患者的提供者不建议参加该试验,2)该患者不符合临床试验的资格,以及3)该患者和照顾者不知道在哪里可以找到临床试验。调查结果强调需要更好的资源和决策支持,这将使患者能够更充分地了解他们参与适当匹配的临床试验的重要性。

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