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Personalized Risk Estimator for Rheumatoid Arthritis (PRE-RA) Family Study: Rationale and design for a randomized controlled trial evaluating rheumatoid arthritis risk education to first-degree relatives

机译:类风湿关节炎的个性化风险估算器(PRE-RA)家庭研究:评估对一级亲属的类风湿关节炎风险教育的随机对照试验的原理和设计

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摘要

We present the rationale, design features, and protocol of the Personalized Risk Estimator for Rheumatoid Arthritis (PRE-RA) Family Study (ClinicalTrials.gov ). The PRE-RA Family Study is an NIH-funded prospective, randomized controlled trial designed to compare the willingness to change behaviors in first-degree relatives of rheumatoid arthritis (RA) patients without RA after exposure to RA risk educational programs. Consented subjects are randomized to receive education concerning their personalized RA risk based on demographics, RA-associated behaviors, genetics and biomarkers or to receive standard RA information. Four behavioral factors associated with RA risk were identified from prior studies for inclusion in the risk estimate: cigarette smoking, excess body weight, poor oral health, and low fish intake. Personalized RA risk information is presented through an online tool that collects data on an individual's specific age, gender, family history, and risk-related behaviors; presents genetic and biomarker results; displays relative and absolute risk of RA; and provides personalized feedback and education. The trial outcomes will be changes in willingness to alter behaviors from baseline to 6 weeks, 6 months, and 12 months in the three intervention groups. The design and execution of this trial that targets a special population at risk for RA, while incorporating varied risk factors into a single risk tool, offer distinct challenges. We provide the theoretical rationale for the PRE-RA Family Study and highlight particular design features of this trial that utilize personalized risk education as an intervention.
机译:我们介绍了类风湿关节炎(PRE-RA)家庭研究的个性化风险估算器的基本原理,设计功能和方案(ClinicalTrials.gov)。 PRE-RA家庭研究是一项由NIH资助的前瞻性,随机对照试验,旨在比较暴露于RA风险教育计划后没有RA的类风湿关节炎(RA)患者一级亲属改变行为的意愿。同意的受试者被随机分配以根据人口统计学,与RA相关的行为,遗传学和生物标记物接受有关其个性化RA风险的教育,或接受标准的RA信息。从先前的研究中确定了与RA风险相关的四个行为因素,将其包括在风险估计中:吸烟,体重过重,口腔健康差和鱼摄入少。个性化RA风险信息通过在线工具提供,该工具收集有关个人特定年龄,性别,家族史和与风险相关的行为的数据;提供遗传和生物标志物结果;显示RA的相对和绝对风险;并提供个性化的反馈和教育。该试验的结果将是在三个干预组中将改变行为的意愿从基线更改为6周,6个月和12个月的意愿。针对以RA特殊危险人群为目标的该试验的设计和执行,同时将各种危险因素纳入单个危险工具中,带来了不同的挑战。我们提供了PRE-RA家庭研究的理论基础,并强调了该试验的特殊设计功能,这些功能利用个性化风险教育作为干预措施。

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