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临床试验/NCT00582829
NCT00582829已完成不适用

Colorectal Cancer Screening Intervention for Family Members of Colorectal Cancer Patients

Memorial Sloan Kettering Cancer Center1 个研究点 分布在 1 个国家目标入组 213 人开始时间: 2003年6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
213
试验地点
1
主要终点
Phone follow-up interview. Participants will be contacted by study assistant and the survey administered.

研究概览

简要总结

This proposed study will use previous study results to guide the development and evaluation of interventions to improve CRC screening acceptance. The proposed study will evaluate the impact of three interventions to promote CRC screening among siblings in this increased-risk group, who are not currently compliant with CRC screening guidelines: 1) a generic print intervention; 2) a tailored print intervention, and; 3) a tailored print plus tailored telephone counseling intervention.

详细描述

First-degree relatives of individuals with CRC are at increased-risk of developing colorectal cancer (CRC). For these increased-risk individuals current guidelines recommend initiating CRC screening a decade earlier than for those at average-risk for CRC; thus, starting at age 40, or 10 years younger than the age at which the affected relative was diagnosed with CRC. In our prior study of 504 at-risk siblings of patients with a history of CRC, diagnosed at age less than 56, we found that approximately 44% of these siblings were not compliant with CRC screening guidelines. Guided by the Transtheoretical, Health Belief and Dual Process models, our prior study identified key attitudinal and non-attitudinal predictors of screening behaviors and intentions.

This proposed study will use these results to guide the development and evaluation of interventions to improve CRC screening acceptance. The proposed study will evaluate the impact of three interventions to promote CRC screening among siblings in this increased-risk group, who are not currently compliant with CRC screening guidelines: 1) a generic print intervention; 2) a tailored print intervention, and; 3) a tailored print plus tailored telephone counseling intervention.

Siblings in the generic print condition will receive a pamphlet about colorectal cancer screening published by the Center for Disease Control. Siblings in the tailored print and telephone counseling conditions will receive messages tailored specifically to their responses on targeted attitudinal and non-attitudinal measures. Five hundred twenty four siblings meeting eligibility criteria will be randomly assigned to one of the three conditions after a baseline interview assessing CRC screening behaviors and attitudes, and it is anticipated that 427 siblings will complete the study. For siblings in the tailored conditions, baseline information will be utilized to design the tailored messages. After receiving the intervention information, participants will be interviewed again six months later regarding CRC screening behaviors and attitudes to assess the impact of the intervention.

研究设计

研究类型
Observational

入排标准

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

入选标准

  • How old is the participant? (≥ 18 years)
  • Is the participant either:
  • currently age 40 or above (YES) OR
  • within 10 years of the age at which the patient/proband was initially diagnosed with CRC (whichever is the younger age) (YES)
  • Is the participant a full or half biological sibling of the patient/proband? (YES)

排除标准

  • Is the participant currently not compliant with standard CRC screening guidelines? (NO)
  • Is the participant English speaking? (YES)
  • Does the participant have a primary language other than English? (NO)
  • Does the participant have a history of Inflammatory Bowel Disease? (NO)
  • Does the participant have a history of colorectal cancer of colorectal polyp? (NO)
  • Does the participant have a history of hereditary colorectal cancer syndrome? (Familial Adenomatous Polyposis or Hereditary Nonpolyposis Colorectal Cancer) (NO)

结局指标

主要结局

Phone follow-up interview. Participants will be contacted by study assistant and the survey administered.

时间窗: 6 months after baseling

次要结局

未报告次要终点

研究者

申办方类型
Other

研究点 (1)

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