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Comparing Methods of Recall for Cancer Screening in Primary Care: a Pragmatic Clinical Trial

Not Applicable
Completed
Conditions
Early Detection of Cancer
Cancer
Socioeconomic 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
NameTimeMethod
The proportion of patients in each arm who go on to receive at least one screening test for which they are due6 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 screening6 months
Secondary Outcome Measures
NameTimeMethod

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

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