跳至主要内容
临床试验/NCT00723996
NCT00723996已完成不适用

Preventive Health Behavior in Women

University of Michigan1 个研究点 分布在 1 个国家目标入组 254 人开始时间: 2003年9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
254
试验地点
1
主要终点
The primary outcome will be determined through review of medical records or a telephone follow-up 6 months after enrollment

研究概览

简要总结

The overall goal of the proposed research is to explore behavioral correlations between colorectal cancer screening and screening mammography.

详细描述

The overall goal of the proposed research is to explore behavioral correlations between colorectal cancer screening and screening mammography and to develop an innovative approach for reducing barriers colorectal cancer screening in women, using screening mammography, an existing non-colon cancer related screening test that has widespread public acceptance, as a "teachable moment." Although screening for colorectal cancer (CRC) has been shown to decrease the incidence of CRC and CRC associated mortality, adherence to screening guidelines from the American Cancer Society and the American Gastroenterological Association remains poor.1-5 Barriers to adherence are not fully defined, but may include poor understanding of the relative benefits and risks of CRC screening, absence of physician recommendation, lack of insurance coverage for screening procedures, and poor patient acceptance of screening procedures. A potential challenge in increasing patient knowledge may be the milieu in which the educational intervention is administered. This study will be the first prospective study to evaluate the effectiveness of an educational intervention designed to increase CRC screening administered at a cancer screening visit unrelated to CRC.

研究设计

研究类型
Observational
时间视角
Prospective

入排标准

年龄范围
50 Years 至 75 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Women between the ages of 50 and 75 years old.
  • Scheduled for a screening mammogram.

排除标准

  • CRC screening current (FOBT within preceding 12 months, FS within 5 years, or colonoscopy within 10 years).
  • Family history of CRC in a first-degree relative.
  • Personal history of colonic adenomatous polyps, CRC or inflammatory bowel disease

结局指标

主要结局

The primary outcome will be determined through review of medical records or a telephone follow-up 6 months after enrollment

时间窗: At 6 month intervals

次要结局

未报告次要终点

研究者

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

Ruth Carlos M.D.

Principal Investigator

University of Michigan

研究点 (1)

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