Evaluation of mailed results versus telephone disclosure of normal cancer genetic test results in a low-risk underserved population.

IF 3.6 3区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Marian J Gilmore, Michael C Leo, Laura M Amendola, Katrina A B Goddard, Jessica Ezzell Hunter, Galen Joseph, Tia L Kauffman, Bradley Rolf, Elizabeth Shuster, Jamilyn M Zepp, Benjamin S Wilfond, Barbara B Biesecker
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引用次数: 0

Abstract

Scalable models for result disclosure are needed to ensure large-scale access to genomics services. Research evaluating alternatives to genetic counseling suggests effectiveness; however, it is unknown whether these findings are generalizable across populations. We assessed whether a letter is non-inferior to telephone genetic counseling to inform participants with no personal or family history of cancer of their normal results. Data were collected via self-report surveys before and after result disclosure (at 1 and 6 months) in a study sample enriched for individuals from underserved populations. Primary outcomes were subjective understanding of results (global and aggregated) and test-related feelings, ascertained via three subscales (uncertainty, negative emotions, and positive feelings) of the Feelings About genomiC Testing Results (FACToR) measure. Secondary outcomes related to satisfaction with communication. Non-inferiority tests compared outcomes among disclosure methods. Communication by letter was inferior in terms of global subjective understanding of results (at 1 month) and non-inferior to telephoned results (at 6 months). Letter was non-inferior to telephone for aggregated understanding (at 6 months). Letter was superior (at 1 month) to telephone on the uncertainty FACToR subscale. Letter was non-inferior to telephone on the positive-feelings FACToR subscale (at 6 months). Letter was non-inferior to telephone for satisfaction with mode of result delivery and genetic test results. Communication via letter was inferior to telephone in communicating the "right amount of information." The use of written communication to relay normal results to low-risk individuals is a promising strategy that may improve the efficiency of care delivery.

在服务不足的低风险人群中,评估邮寄结果与电话披露正常癌症基因检测结果的对比。
需要可扩展的结果披露模式,以确保基因组学服务的大规模普及。对遗传咨询替代方案的评估研究表明,这些方案是有效的;但这些研究结果是否可在不同人群中推广尚不清楚。我们评估了在告知无个人或家族癌症病史的参与者其正常结果时,信件是否不逊于电话遗传咨询。数据是在结果披露前后(1 个月和 6 个月)通过自我报告调查收集的,研究样本中包括来自服务不足人群的个人。主要结果是对结果的主观理解(整体和综合)以及与检测相关的感受,通过基因组学检测结果感受量表(FACToR)的三个分量表(不确定性、消极情绪和积极情绪)确定。次要结果与沟通满意度有关。非劣效性测试比较了不同披露方法的结果。就对结果的总体主观理解而言,信件沟通的效果较差(1 个月),但不逊于电话沟通的效果(6 个月)。在综合理解方面(6 个月时),信件沟通不逊于电话沟通。在不确定性 FACToR 子量表方面,信件(1 个月时)优于电话。在积极感受 FACToR 分量表上,信件并不比电话效果差(6 个月时)。在对结果交付方式和基因检测结果的满意度方面,信件并不比电话差。在传达 "适量信息 "方面,信件沟通不如电话沟通。使用书面沟通方式向低风险人群传达正常结果是一种很有前景的策略,可以提高医疗服务的效率。
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来源期刊
Translational Behavioral Medicine
Translational Behavioral Medicine PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH -
CiteScore
6.80
自引率
0.00%
发文量
87
期刊介绍: Translational Behavioral Medicine publishes content that engages, informs, and catalyzes dialogue about behavioral medicine among the research, practice, and policy communities. TBM began receiving an Impact Factor in 2015 and currently holds an Impact Factor of 2.989. TBM is one of two journals published by the Society of Behavioral Medicine. The Society of Behavioral Medicine is a multidisciplinary organization of clinicians, educators, and scientists dedicated to promoting the study of the interactions of behavior with biology and the environment, and then applying that knowledge to improve the health and well-being of individuals, families, communities, and populations.
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