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OpenTrials
Completed

NCT Number: NCT00723996

Preventive Health Behavior in Women

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

Completed

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Key information

Age range

50 year–75 year

Sex eligibility

Female

Study type

Observational

Primary location

University of Michigan Health System

Ann Arbor, Michigan, 48109, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • 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

Treatment and study plan

Behavioral Study in Women

Behavioral

A Randomized study to assess the knowledge of womens health related issues

Primary outcomes

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

    Time frame: At 6 month intervals

Sponsors and collaborators

Lead sponsor

University of Michigan

Other

Registry information

Important dates

Study start
2003
Primary completion
2016
Study completion
2016
First posted
Jul 29, 2008
Registry last updated
Dec 16, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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