Comparing Methods of Recall for Cancer Screening in Primary Care: a Pragmatic Clinical Trial
Not Applicable
Completed
- Conditions
- Early Detection of CancerCancerSocioeconomic Status
- Registration Number
- NCT02457143
- Lead Sponsor
- Unity Health Toronto
- Brief Summary
This randomized trial aims to understand how effective a reminder letter is compared to a reminder phone call in improving breast, cervical and colorectal cancer screening rates and reducing screening disparities.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 5270
Inclusion Criteria
- The trial will include patients who are rostered to the family practice as of March 31, 2015, are eligible and overdue for cervical, breast and/or colorectal cancer screening and are verified by their primary care physician as needing recall.
Exclusion Criteria
- Patients will be excluded if their primary care physician noted they should not be recalled for screening or if the patient does not have both an address and a phone number on file.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method The proportion of patients in each arm who go on to receive at least one screening test for which they are due 6 months The proportion of patients in each arm who are due for breast, cervical and colorectal cancer screening who go on to receive those respective screening tests (female patients may be represented in the outcome calculation of more than one cancer screening 6 months
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
St. Michael's Hospital Academic Family Health Team
🇨🇦Toronto, Ontario, Canada
St. Michael's Hospital Academic Family Health Team🇨🇦Toronto, Ontario, Canada