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临床试验/NCT03100461
NCT03100461已完成不适用

Adaptive Intervention to Maximize Colorectal Screening in Safety Net Populations

University of Kansas Medical Center1 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2018年1月22日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
500
试验地点
1
主要终点
CRC screening completion rate

研究概览

简要总结

The goal of this study is to find the best ways to increase colorectal cancer (CRC) screening.

详细描述

Colorectal Cancer is preventable and curable but is still the second most common cause of cancer death in the U.S. Minorities and those with low income have more CRC than middle and high income Whites.. They also get fewer CRC screening tests. Low knowledge of CRC screening may, in part, drive this lower test use. We need new ways to improve CRC screening in primary care clinics where many minority and uninsured patients receive health care.

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
Double (Participant, Care Provider)

入排标准

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

入选标准

  • Have a home address and access to a working telephone
  • Pass Mini-Cog assessment

排除标准

  • FIT (fecal immunochemical test) test within 1 year, Sigmoidoscopy or Barium enema within 5 years, or Colonoscopy within 10 years
  • Acute medical illness,
  • current GI bleed
  • history of adenomatous polyps
  • Colorectal Cancer
  • 1st degree relative with CRC < age 60 years
  • inherited polyposis/non-polyposis syndrome
  • inflammatory bowel disease
  • Another household member enrolled in the study

研究组 & 干预措施

HE + I2

Active Comparator

Participants receive up to two interventions. Participants receive HE initially and then I2 if not screened after 6 months.

干预措施: I2 (Other)

HE + HE

Active Comparator

Participants receive up to two interventions. Participants receive HE initially and then a second time if not screened after 6 months.

干预措施: Health Education (Other)

HE + I2

Active Comparator

Participants receive up to two interventions. Participants receive HE initially and then I2 if not screened after 6 months.

干预措施: Health Education (Other)

I2 + HE

Active Comparator

Participants receive up to two interventions. Participants receive I2 initially and then HE if not screened after 6 months.

干预措施: Health Education (Other)

I2 + HE

Active Comparator

Participants receive up to two interventions. Participants receive I2 initially and then HE if not screened after 6 months.

干预措施: I2 (Other)

I2 + I2

Experimental

Participants receive up to two interventions. Participants receive I2 initially and then a second time if not screened after 6 months.

干预措施: I2 (Other)

结局指标

主要结局

CRC screening completion rate

时间窗: 12-14 Months

Rate of participants who receive CRC screening during study participation

次要结局

  • Cost analysis of each intervention pathway(14 Months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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