Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Emory University
With
National Cancer Institute (NCI)
National Institutes of Health (NIH)
PRIMARY OBJECTIVES; I. Compare the screening mammogram (SM) completion rates between PReVenT and enhanced usual care (EUC) arms at 6 months.
II. Describe patient's experience with the PReVenT intervention using mixed methods stratified by completion of SM.
OUTLINE: Participants are randomized to 1 of 2 arms.
ARM I: Participants receive usual care as well as a portal message reminder to schedule a SM and a callback link if they need assistance. Participants who have not or do not schedule their SM at the time of the first reminder receive a reminder text-message one week later with a link to receive assistance with scheduling.
ARM II: Participants receive usual care as well as portal and text messages one week apart with educational materials about healthy eating.
After completion of study, patients are followed up at 6 months.
Age
50–74
Sex
FEMALE
Healthy volunteers
Accepted
You may be eligible if
Women aged 50-74 years
Active online patient portal account
Mobile phone number listed in the electronic medical record (EMR)
At least one primary care visit in our healthcare system between 2015 and 2021
No screening mammography performed in our healthcare system in the last 2 years
You may not be if
Because of limited research team and patient portal language at this time, non-English speaking patient will be excluded
Personal history of breast cancer or prior mastectomy
Participants who already have an upcoming SM scheduled within or outside of Emory Healthcare
Patients who had a screening mammography at an outside facility within the prior 2 years
Patients with severe comorbidities at the time of the study (in palliative care or hospitalized at the time of the study)
Participants who are cognitively impaired or have with history of Alzheimer's disease or dementia
