Genetic Epidemiology Risk Assessment Program or Usual Care in Colorectal Cancer Screening for Healthy Participants



Status:Completed
Conditions:Colorectal Cancer, Cancer, Healthy Studies
Therapuetic Areas:Oncology, Other
Healthy:No
Age Range:50 - Any
Updated:4/21/2016
Start Date:March 2007

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Gene Environment Risk Assessment and CRC Screening

RATIONALE: The Genetic Epidemiology and Risk Assessment program may be more effective than
usual care in increasing the number of healthy participants who regularly receive screening
for colorectal cancer.

PURPOSE: This randomized clinical trial is studying the Genetic Epidemiology and Risk
Assessment program to see how well it works compared with usual care to increase colorectal
cancer screening in healthy participants.

OBJECTIVES:

- Compare Genetic Epidemiology and Risk Assessment (GERA) feedback vs usual care (UC) in
terms of colorectal cancer (CRC) screening utilization by healthy participants.

- Determine the impact of GERA feedback and UC on psychological distress in these
participants.

- Compare GERA feedback vs UC in terms of intention to have CRC screening, perceived CRC
risk, CRC knowledge, salience and coherence of CRC screening, and support for CRC
screening in these participants.

- Identify factors that moderate the impact of GERA feedback on CRC screening
utilization.

OUTLINE: This is a randomized study. Participants are randomized to 1 of 2 screening arms.

- Arm I: Participants receive standard primary care.

- Arm II: Participants receive standard primary care followed by the Genetic Epidemiology
and Risk Assessment (GERA) intervention. Participants also participate in a discussion
session regarding the GERA including the rationale behind methylenetetrahydrofolate
reductase mutation detection and folate assessment and its relationship to colorectal
cancer risk.

All participants undergo a fecal occult blood test 3 weeks after the screening office visit.

PROJECTED ACCRUAL: A total of 1,950 participants will be accrued for this study.

DISEASE CHARACTERISTICS:

- Healthy participants meeting the following criteria:

- No personal history of colorectal polyps or cancer or inflammatory bowel disease

- No family history of familial adenomatous polyposis, hereditary nonpolyposis
colorectal cancer (CRC), or CRC in more than 1 first-degree relative

- Nonadherent with standard CRC screening recommendations at the time of their index
office visit

PATIENT CHARACTERISTICS:

- Able to communicate with ease in English

PRIOR CONCURRENT THERAPY:

- More than 6 weeks since prior antibiotics or antifolate medications (e.g.,
sulfasalazine, methotrexate)
We found this trial at
1
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Philadelphia, Pennsylvania 19111
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Philadelphia, PA
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