A tool for false positive rate estimation in cognitive impairment research: Handling correlated tests, small samples, and composite criteria.

IF 3 3区 心理学 Q2 CLINICAL NEUROLOGY
Joost A Agelink van Rentergem, Sanne B Schagen
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引用次数: 0

Abstract

Background: In the field of clinical neuropsychology, researchers and clinicians often use predefined criteria to determine whether there are indications of cognitive impairment. However, corrections and expected false-positive rates are typically available only for uncorrelated tests and simple consensus criteria. Objective: To present an easy-to-use and freely available online tool as a solution for scenarios involving correlated tests and composite consensus criteria, as frequently encountered in clinical neuropsychological research and practice. Method: Our tool employs Monte Carlo simulations to account for the number of participants, thus addressing the uncertainty in estimating false positive rates with small samples. We demonstrate the tool's utility through an example involving cognitive impairment assessment in cancer patients after chemotherapy. Results: The tool reveals considerable uncertainty in false positive rates, especially with small sample sizes, where rates may be higher than traditionally assumed. We found that correlations between tests affect impairment rates differently depending on whether single or multiple test criteria are used. For single-test criteria, lower correlations are associated with more false positives, while for multiple-test criteria, lower correlations lead to fewer false positives. Conclusions: This innovative tool enables more accurate estimation of false positive rates in various neuropsychological conditions. By providing a user-friendly interface and accounting for real-world complexities such as test correlations and composite criteria, our tool empowers clinicians and researchers to: Make informed decisions when interpreting neuropsychological test results.Design more robust research protocols for cognitive impairment studies.Better understand the implications of sample size on false positive rates.

认知障碍研究中假阳性率估计的工具:处理相关测试、小样本和复合标准。
背景:在临床神经心理学领域,研究人员和临床医生经常使用预定义的标准来确定是否存在认知障碍的迹象。然而,校正和预期的假阳性率通常只适用于不相关的测试和简单的一致标准。目的:提供一个易于使用和免费的在线工具,作为临床神经心理学研究和实践中经常遇到的涉及相关测试和复合共识标准的场景的解决方案。方法:我们的工具采用蒙特卡罗模拟来解释参与者的数量,从而解决了小样本估计假阳性率的不确定性。我们通过一个涉及化疗后癌症患者认知障碍评估的例子来证明该工具的实用性。结果:该工具揭示了假阳性率相当大的不确定性,特别是在小样本量下,其率可能高于传统假设。我们发现测试之间的相关性对损伤率的影响不同,这取决于是否使用单一或多个测试标准。对于单一测试标准,较低的相关性与更多的假阳性相关,而对于多个测试标准,较低的相关性导致更少的假阳性。结论:这种创新的工具可以更准确地估计各种神经心理状况下的假阳性率。通过提供用户友好的界面,并考虑现实世界的复杂性,如测试相关性和复合标准,我们的工具使临床医生和研究人员能够:在解释神经心理学测试结果时做出明智的决定。为认知障碍研究设计更可靠的研究方案。更好地理解样本量对假阳性率的影响。
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来源期刊
Clinical Neuropsychologist
Clinical Neuropsychologist 医学-临床神经学
CiteScore
8.40
自引率
12.80%
发文量
61
审稿时长
6-12 weeks
期刊介绍: The Clinical Neuropsychologist (TCN) serves as the premier forum for (1) state-of-the-art clinically-relevant scientific research, (2) in-depth professional discussions of matters germane to evidence-based practice, and (3) clinical case studies in neuropsychology. Of particular interest are papers that can make definitive statements about a given topic (thereby having implications for the standards of clinical practice) and those with the potential to expand today’s clinical frontiers. Research on all age groups, and on both clinical and normal populations, is considered.
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