Trial Information
Activating Rural Clinics and Women With Disabilities to Improve Cancer Screening
Inclusion Criteria:
- Female
- Aged 50-75 at time of screening
- No personal history of breast, cervical or colorectal cancer
- Not being up-to-date with at least one screening test for breast, cervical, and/or
colorectal cancer
- Meets the study definition of disability per APCC-1 (intervention group) OR
- Be a woman who does not meet the definition of disability on APCC-1, but has been
matched to a participant who does (observation group).
Exclusion Criteria:
- Non female
- Personal history of breast, cervical, or colorectal cancer
Type of Study:
Observational
Study Design:
Observational Model: Ecologic or Community, Time Perspective: Prospective
Outcome Measure:
Number of participants with improved cancer screening
Outcome Description:
A 2 x 2 factorial study design will be used to explore individual and combined effects of a clinic-based intervention AND a patient-based intervention on improving breast, cervical and colorectal cancer screening among rural women with physical disabilities (WWD).
Outcome Time Frame:
Duration of the study; Up to 1 year
Safety Issue:
No
Principal Investigator
David Buckley, MD
Investigator Role:
Principal Investigator
Investigator Affiliation:
Oregon Health and Science University
Authority:
United States: Institutional Review Board
Study ID:
IRB00009030
NCT ID:
NCT01773980
Start Date:
January 2013
Completion Date:
August 2014
Related Keywords:
- Breast Cancer
- Cervical Cancer
- Colorectal Cancer
- Breast Neoplasms
- Uterine Cervical Neoplasms
- Colorectal Neoplasms
Name | Location |
OHSU Knight Cancer Institute |
Portland, Oregon 97239 |