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首页> 外文期刊>Trials >Patients’ and physicians’ disagreement on patients’ understanding of clinical cancer trial information: a pairwise pilot study of mirroring subjective assessments compared with objective measurements
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Patients’ and physicians’ disagreement on patients’ understanding of clinical cancer trial information: a pairwise pilot study of mirroring subjective assessments compared with objective measurements

机译:患者和医生对患者对临床癌症试验信息的理解存在分歧:将主观评估与客观测量结果进行对比的成对先导研究

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Informed consent is a prerequisite for patients included in clinical trials. Trial design, inclusion criteria and legal requirements are increasingly complex. This complexity challenges design and delivery of written and oral trial information to ensure understandable information. To evaluate the level of concordance between patients’ and informing physicians’ assessments regarding patient understanding of trial information, we carried out a study based on paired questionnaire data from patients and their physicians. These assessments of patient understanding were further correlated with patients’ factual knowledge of the information provided. This pilot study included patients and physicians immediately after the patients had received information on one of 23 ongoing phase III randomised cancer trials at two Swedish sites. In total, 46 patients and 17 physicians contributed data based on two new questionnaires with seven mirroring questions, where concordance was analysed with McNemar’s test. These assessments of patients’ self-estimated understanding were further correlated with the Patient Understanding of Research (Q-PUR) questionnaire that assesses factual knowledge of the information provided. For each question, 47–61% of the patient–physician pairs were in concordance regarding their assessments of patients’ ‘fully understanding’ or ‘not fully understanding’ various aspects of the trial information. For the discordant pairs, the physicians rated patient understanding lower than the patients themselves, for all seven questions. This difference was significant for five of the questions (P?≤?0.017). The median Q-PUR knowledge score was 11 out of 12, but this score did not significantly correlate with the assessments, either from patients or from physicians. This study demonstrated a trend for physicians to rate the level of understanding of trial information among potential trial patients lower than the patients themselves. Application of Q-PUR revealed high knowledge scores, but without correlation to the assessments. These findings need validation in an independent setting, with an improved instrument with mirroring questions, and a better-matched measurement of patients’ factual knowledge. These results suggest that physicians need to improve their ability to assess patient understanding of clinical trial information, in order to be able to tailor the patients’ information individually.
机译:知情同意是纳入临床试验患者的先决条件。审判设计,纳入标准和法律要求越来越复杂。这种复杂性挑战了书面和口头审判信息的设计和交付,以确保信息易于理解。为了评估患者和告知医生有关患者对试验信息理解的评估之间的一致性水平,我们基于来自患者及其医师的配对问卷数据进行了一项研究。这些对患者理解的评估与患者对所提供信息的事实知识进一步相关。这项初步研究包括患者和医生,在患者获得了在两个瑞典站点进行的23个正在进行的III期随机癌症试验之一的信息之后。总共有46位患者和17位医生根据两份包含七个反映问题的新调查表提供了数据,并通过McNemar的测试分析了一致性。这些对患者自我评估理解的评估与“研究患者理解”(Q-PUR)调查表进一步相关,该调查表评估了所提供信息的事实知识。对于每个问题,在47%至61%的医患对中,他们对患者对试验信息各个方面的“完全理解”或“不完全理解”的评估是一致的。对于不一致的对,医生对所有七个问题的评价都低于患者本人。对于五个问题(P≤0.017),这种差异是显着的。 Q-PUR知识评分的中位数是12分中的11分,但是该分值与患者或医生的评估均无显着相关性。这项研究证明了一种趋势,即医师对潜在的受试患者中对试验信息的理解程度进行了评估,该水平低于患者本身。 Q-PUR的应用显示出较高的知识得分,但与评估没有关联。这些发现需要在独立的环境中进行验证,需要使用带有镜像问题的改进工具以及对患者的事实知识进行更好匹配的评估。这些结果表明,医生需要提高他们评估患者对临床试验信息的了解的能力,以便能够分别定制患者的信息。

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