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临床试验/NCT01274143
NCT01274143已完成不适用

Impact of Remote Familial Colorectal Cancer Assessment and Counseling

University of Utah16 个研究点 分布在 1 个国家目标入组 496 人开始时间: 2008年5月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
496
试验地点
16
主要终点
Colonoscopy

研究概览

简要总结

The Family Colorectal Cancer Awareness and Risk Education Project (Family CARE Project) is designed to determine whether a personalized telephone plus mailed print cancer risk assessment and behavior change counseling intervention is more effective than a targeted mailed print intervention in promoting risk appropriate screening in individuals with a family history of the disease. The project targets people residing in both rural and urban areas, allowing an examination of differential intervention effects with regard to place of residence.

详细描述

The rate of adherence to regular colonoscopy screening (CS) among members of families at increased risk for colorectal cancer (CRC) is far below recommended levels. Persons who live in rural areas of the United States exhibit lower CRC screening rates than their urban counterparts. Although the detection of familial predisposition to cancer begins with an accurate family medical history, data indicate that many patients do not receive adequate familial cancer risk assessment from their primary care providers. This suggests that familial risk is largely unrecognized which may lead to inadequate risk stratification, lack of risk notification, appropriate risk counseling, suboptimal cancer screening and preventable deaths. Because of geographic and system-level barriers, special efforts are needed to improve access to personalized risk communication and adherence to CRC screening to rural and other geographically underserved populations at increased risk for CRC. In the proposed study, we will evaluate a novel telephone-based, theory-guided personalized risk communication intervention that combines a familial CRC risk assessment and behavioral counseling with tailored messages. The key hypothesis guiding this study is that a multifaceted personalized risk communication intervention will improve CS at a significantly higher rate than a mailed targeted print intervention.

Our integrative study model specifies important theoretical mechanisms that can contribute to increased use of CS among persons at increased risk. We will enroll 438 adult men and women between the ages of 30-74 who are considered at increased risk of familial CRC into this 2-group randomized trial. The primary aim of this study is to compare colonoscopy use among participants in the two groups. Secondary aims are to compare the two groups with regard to cognitive and emotional outcomes and explore the underlying mechanisms through which the interventions have an impact on colonoscopy behavior. Sociodemographic, clinical, behavioral and psychosocial measures will be collected from participants at baseline, and 1 month, 9 months, and 15 months following the intervention. Self-reported colonoscopy is verified with medical records.

The study's findings will have both theoretical, as well as practical significance. Our findings will help to influence the selection and dissemination of effective outreach approaches to improve CRC screening in populations at increased risk for the disease. These results have broad applicability to understanding responses to personalized risk communication interventions for other diseases as well. Findings will also broaden our understanding of the underlying theoretical mechanisms of how remote cancer risk communications lead to improvements in cancer screening among geographically underserved populations if such intervention effects are observed.

In addition to studying the intervention effects in rural areas, we will enroll participants in urban areas. These enhancements to our population-based randomized behavioral trial will provide us with an unprecedented opportunity to assess reach and determine if there are differential intervention effects (i.e., efficacy) with regard to place of residence (rurality vs. urbanicity.)

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
30 Years 至 74 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Have at least one first-degree relative diagnosed with colorectal cancer (CRC) between the ages of 40-59, or one first-degree relative diagnosed with colorectal cancer at age 40 or older and an additional first-degree or second-degree relative diagnosed with colorectal cancer at age 40 or older.
  • If relative was diagnosed over age 50, participant must be 40-74 years old.
  • If relative was diagnosed at age 40-49, participant cannot be more than ten years younger than relative at first diagnosis (e.g., dx at 48, participant must be 38-74 years old).
  • Colorectal cancer cases of relatives recruited through the cancer registries of California, Colorado, Idaho, New Mexico, or Utah; Rocky Mountain Cancer Genetics Coalition sites of National Cancer Genetics Network in Colorado, New Mexico, or Utah; or Intermountain Health Care

排除标准

  • Previous cancer diagnosis of any kind (except for non-melanoma skin cancers).
  • Has had a colonoscopy within the past five years.
  • Meets clinical criteria for Lynch syndrome or other polyposis syndromes.
  • Has had prior involvement in colorectal cancer-related clinical, behavioral or epidemiologic cancer familial research.
  • Mentally incompetent, incarcerated, hearing or visually impaired.
  • Unable to read and speak English fluently.

结局指标

主要结局

Colonoscopy

时间窗: 9 month follow-up

The primary outcome is colonoscopy. Medical record verification of self-reported colonoscopy is performed.

次要结局

  • Fecal occult blood test (FOBT)/Fecal Immunochemical Test (FIT)(Baseline, 1 month, 9 month, and 15 month follow-up)
  • Perceived Control(Baseline, 1 month and 9 month follow-up)
  • Perceived Risk(Baseline, 1 month and 9 month follow-up)
  • Psychological distress(Baseline, 1 month and 9 month follow-up)
  • Knowledge(Baseline, 1 month and 9 month follow-up)
  • Decisional Conflict(Baseline, 1 month and 9 month follow-up)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Anita Kinney

Professor

University of Utah

研究点 (16)

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