360
Participants
Start Date
July 31, 2010
Primary Completion Date
July 31, 2026
Study Completion Date
July 31, 2026
survey, questionaire
The intervention components (mailed tailored print materials followed by telephone-delivered Brief MI). Following enrollment into the study and completion of the informed consent form and baseline survey, participants will be randomized to the active intervention group or the attention control group. The data that will be used in the analysis will come from the baseline survey, medical records of breast imaging studies, and a 12-month follow-up questionnaire.
survey, questionaire
The intervention components (mailed tailored print materials followed by telephone-delivered Brief MI). Following enrollment into the study and completion of the informed consent form and baseline survey, participants will be randomized to the active intervention group or the attention control group. The data that will be used in the analysis will come from the baseline survey, medical records of breast imaging studies, and a 12-month follow-up questionnaire.
St. Jude Children's Research Hospital, Memphis
St. Jude Children's Research Hospital
OTHER
University of Colorado, Denver
OTHER
Dana-Farber Cancer Institute
OTHER
University of Chicago
OTHER
Memorial Sloan Kettering Cancer Center
OTHER