Community Dissemination of an Evidence-based CRC Screening Intervention
Interventional
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Screening
Change from Baseline in receipt of CRC screening at 6 months and 24 months
Subjects will receive any one of the 3 recommended CRC screening tests namely, Fecal Occult Blood Test, Flexible sigmoidoscopy or Colonoscopy
baseline, 6-month and 24-month post intervention
No
Annette E Maxwell, Dr.P.H.
Principal Investigator
University of California, Los Angeles
United States: Institutional Review Board
RSGT CPPB-119384
NCT01351220
July 2010
June 2014
Name | Location |
---|---|
UCLA Division of Cancer and Prevention Research | Los Angeles, California 90095-6900 |