Testing a Behavioural Approach to Improving Cancer Screening Rates

NCT03124316 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 5525

Last updated 2018-03-22

No results posted yet for this study

Summary

Family doctors can play a critical role in successfully arranging cancer screening tests to occur, especially if they know which patients are due for these tests. However, they don't always interact with or take advantage of registry data to this end. For example, in Ontario, the Screening Activity Report provides exactly this information to family doctors, helping them identify their patients who are overdue for screening. Unfortunately, less than half of family doctors regularly use the Screening Activity Report even though they get monthly email reminders. One possible reason is that the reminders they receive are not designed to compel action. They are easy for family doctors to miss or dismiss. This study will compare multiple different ways of designing the reminders. The different versions of the email are tested in a 2\^3 factorial trial testing three behaviour change techniques to see which ones will lead to more family physicians interacting with the Screening Activity Report and at increasing the number of patients that get all the appropriate screening tests for cervical, breast, and/or colon cancer.

Conditions

  • Early Detection of Cancer
  • Clinical Trial

Interventions

BEHAVIORAL

Anticipated regret

Induce awareness of future regret about the unwanted behaviour

BEHAVIORAL

Material incentive

Inform that valued objects will be delivered if and only if that has been progress in performing the desired behaviours

BEHAVIORAL

Problem solving

Analyze or prompt the person to factors that influence the behaviour and select strategies that help overcome barriers

Sponsors & Collaborators

  • Ontario Institute for Cancer Research

    collaborator OTHER
  • Cancer Care Ontario

    collaborator OTHER
  • Ottawa Hospital Research Institute

    collaborator OTHER
  • Laval University

    collaborator OTHER
  • Women's College Hospital

    lead OTHER

Principal Investigators

  • Noah Ivers, MD, PhD · Women's College Hospital

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
DOUBLE
Model
FACTORIAL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-05-10
Primary Completion
2017-09-30
Completion
2017-09-30

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03124316 on ClinicalTrials.gov