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OpenTrials
Completed

NCT Number: NCT03124316

Testing a Behavioural Approach to Improving Cancer Screening Rates

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.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cancer Care Ontario

Toronto, Ontario, M5G 2L7, Canada

About this study

Screening is an important way to prevent cancer-related death, but many Ontarians do not receive guideline-recommended screening for cervical, breast, and colon cancer. Family physicians can play a critical role in successfully increasing screening rates. A recent evaluation by members of our team suggests that Screening Activity Report (SAR) use is associated with improved cancer screening, but there remains substantial room for improvement. For the SAR to reach its full potential to decrease cancer-related death by improving screening rates, family physicians must regularly access it and take the appropriate actions. Currently, family physicians receive monthly email reminders, which state that new data are available, but do not describe the benefits of the SAR for physicians or their patients. It is easy to imagine how a busy doctor would fail to act upon such emails, resulting in suboptimal use of the SAR and leading to avoidable delays in cancer screening, and management. Indeed, CCO data show that less than half of recipients attend to this email and <7% click through to the SAR. The objectives for this trial are to compare different versions of the reminders in a randomized trial to identify the features that most increase use of the SAR. This is a pragmatic, 2^3 factorial trial, comparing behaviour change techniques incorporated within email reminders to doctors increase their use of the SAR. Participants are those who are already sent monthly emails by CCO regarding the SAR. The trial will randomly assign participants to one of eight modified emails to determine which content is most effective at driving SAR-use over 4 months. With an expected sample size of over 5700 family physicians, we anticipate power to see differences of 3% across experimental conditions.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Family physicians are eligible if they have signed up for the SAR and already receive reminder emails as part of their registration process for the SAR with CCO.

Treatment and study plan

Anticipated regret

Behavioral

Induce awareness of future regret about the unwanted behaviour

Material incentive

Behavioral

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

Problem Solving

Behavioral

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

Primary outcomes

  1. SAR access

    Time frame: 4 months

    The primary outcome will be whether eligible family physicians access the SAR during the 4 months of the trial (Yes/No)

Secondary outcomes

  1. SAR access rate

    Time frame: 4 months

    Number of times the SAR was accessed

  2. Adherence to screening guidelines for breast, colon, and cervical cancer in patients of eligible PCPs

    Time frame: 4 months

    Proportion of patients meeting screening guidelines for breast, colon, and cervical cancer; and efforts made by participants to access the SAR-use

Other outcomes

  1. Process Measures: contact made with Cancer Care Ontario

    Time frame: 4 months

    Number of calls to CCO contact centre regarding the SAR

Sponsors and collaborators

Lead sponsor

Women's College Hospital

Other

Collaborators

  • Cancer Care Ontario
  • Laval University
  • Ontario Institute for Cancer Research
  • Ottawa Hospital Research Institute

Registry information

Official study title

Testing a Behavioural Approach to Improving Cancer Screening Rates Through Increased Use of Primary Care Feedback Reports

Important dates

Study start
2017
Primary completion
2017
Study completion
2017
First posted
Apr 21, 2017
Registry last updated
Mar 22, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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