BREAST CANCER PATIENTS RELATIVES--RESPONSE OVER TIME

针对癌症风险较高或接受能力较强的人群的信息可以提高预防和早期发现工作的效率和效力。癌症患者的亲属在诊断时可能是一个接受人群，因为他们对癌症风险的认识更高，更突出。公共卫生和患者干预战略必须了解：1）适应亲属诊断的复杂过程; 2）可能有特殊需求的人口亚群的特征变量。虽然这些问题已经在一定程度上研究了乳腺癌患者的亲属，重要的问题仍然存在，包括什么因素的影响和相互作用的感知风险和情绪困扰随着时间的推移，应对方式和健康行为在适应过程中的作用。众所周知，风险认知和情绪困扰在亲属之间差异很大，但不同亚组内的问题尚未得到表征。缺乏关于这些问题的资料部分是由于横截面设计的固有局限性。我们提出了一个前瞻性的，纵向调查的过程中的适应在520个一级女性亲属约422乳腺癌“指数”患者。我们将追求以下具体目标：在癌症患者的亲属中：1）评估与感知风险相关的态度，知识，情绪困扰和应对; 2）确定12个月内筛查参与和生活方式行为变化的自然史; 3）进行广泛的，理论驱动的多因素分析，以建立信念和行为如何随着时间的推移而受到影响的模型。在乳腺癌患者中：1）评估患者的一般痛苦水平，对乳腺癌的知识/看法，以及给亲属的建议; 2）探索患者的报告与亲属的信仰和调整的关系。患者将在初步诊断后六周内亲自联系和面谈。将在基线（T0）、6个月（T1）和12个月（T2）随访时通过电话采访其亲属。本研究的结构是从社会信息处理和个体差异的社会认知公式中选择的，特别是米勒的C-SHIP模型。大多数措施都是标准化的工具，有效性和可靠性受到尊重。数据分析将重点关注假设路径的多变量建模，使用随时间推移的面板设计，以及样本的具有临床意义的亚组内模式的表征。

Targeting messages to people at higher risk of cancer or with increased receptivity can enhance the efficiency and effectiveness of prevention and early detection efforts. Relatives of cancer patients near the time of diagnosis may be a receptive population due to a higher and more salient sense of their cancer risk. Public health and patient intervention strategies must be informed by understanding: 1) the complex process of adaptation to a relative's diagnosis; and 2) the variables that characterize subgroups of the population who may have specific needs. While these issues have been studied to some extent in relatives of breast cancer patients, important questions remain, including what factors influence and interact with perceived risk and emotional distress over time, the role of coping style and health behavior in the adaption process. It is known that risk perception and emotional distress vary widely among relatives, but the issues within distinct subgroups have not been characterized. The lack of information on these questions is partly due to the inherent limitations of cross- sectional designs. We propose a prospective, longitudinal investigation of the process of adaptation in a 520 first-degree female relatives of approximately 422 breast cancer "index" patients. We will pursue the following specific aims: Among relatives of cancer patients to: 1) Assess attitudes, knowledge, emotional distress, and coping, in relation to perceived risk; 2) Determine the natural history of screening participation and lifestyle behavior change over 12 months; 3) Engage in an extensive, theory-driven multi-factorial analysis to build models of how beliefs and behaviors are influenced over time. Among breast cancer patients, to: 1) Assess the patient's general level of distress, knowledge/perceptions about breast cancer, and advice given to relatives; and 2) Explore the relationship of the patient's report to their relatives' beliefs and adjustment. Patients will be contacted and interviewed in person within six weeks of their initial diagnosis. Their relatives will be interviewed by telephone at baseline (T0), and at 6-month (T1) and 12-month (T2) follow-ups. Constructs for the study have been selected from social cognitive formulations of social information processing and individual difference, specifically Miller's C-SHIP model. A majority of measures are standardized tools with respected validity and reliability. Data analysis will focus on the multi-variate modeling of the hypothesized paths, using a panel design over time, as well as on the characterization of patterns within clinically meaningful subgroups of the sample.