MyMammogram for Breast Cancer
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a tool called MyMammogram to determine if it aids women and their doctors in making better breast cancer screening decisions. It compares three groups: one using MyMammogram with additional doctor communication, one using MyMammogram alone, and one receiving usual care. Women aged 39-49, with an upcoming doctor's appointment, who haven't had a mammogram in the past year, and haven't had breast cancer, are suitable candidates. The trial focuses on how this tool functions in rural healthcare settings. Participants will share their thoughts on the process to help refine the trial. As an unphased trial, this study allows participants to contribute to innovative research that could improve breast cancer screening decisions.
Do I need to stop my current medications to join the trial?
The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.
What prior data suggests that the MyMammogram protocol is safe for patients?
Research shows that mammography screening, part of the MyMammogram process, is generally safe for most people. Studies have found that mammography can significantly reduce the risk of dying from breast cancer. However, some possible downsides exist. For example, a false-positive result might occur, suggesting cancer is present when it isn't. Additionally, the procedure uses a small amount of radiation, similar to other common medical imaging tests. Although these risks are considered low, it's important to be aware of them when considering participation in a trial involving MyMammogram.12345
Why are researchers excited about this trial?
Researchers are excited about MyMammogram because it leverages technology to enhance early breast cancer detection. Unlike standard mammography, which relies solely on imaging, MyMammogram combines digital assessment tools with provider communication. This innovative approach not only empowers patients by providing them with actionable insights before their appointments but also equips healthcare providers with a comprehensive summary beforehand. By potentially streamlining the diagnostic process, MyMammogram could lead to quicker and more personalized patient care.
What evidence suggests that this trial's treatments could be effective for breast cancer?
Research shows that mammography screening helps reduce deaths from breast cancer. Studies have found that regular mammograms can detect cancer earlier, which links to lower death rates. For instance, screening women aged 40 to 79 can prevent about 11.5 breast cancer deaths per 1,000 women. Early detection through mammograms often allows for easier treatment. Overall, regular mammography is a proven method in the fight against breast cancer. This trial will evaluate the effectiveness of MyMammogram, with one group using MyMammogram before their appointment and another group using MyMammogram with additional provider communication. A third group will receive usual care.36789
Are You a Good Fit for This Trial?
This trial is for English or Spanish-speaking women aged 39-49 who have an upcoming appointment with a participating primary care provider within the next four weeks. It's designed to help those living in rural areas make informed decisions about mammograms.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Intervention
Participants use the MyMammogram decision aid, with or without provider communication, prior to their primary care visit
Follow-up
Participants are monitored for intervention acceptability and other outcomes through surveys and interviews
What Are the Treatments Tested in This Trial?
Interventions
- MyMammogram
Find a Clinic Near You
Who Is Running the Clinical Trial?
Dartmouth-Hitchcock Medical Center
Lead Sponsor
Trustees of Dartmouth College
Collaborator