Trial Information
EMPOWER Study: Promoting Breast Cancer Screening in Women Who Survived Childhood Cancer
Inclusion Criteria:
- Participant in the CCSS cohort
- Diagnosed with a childhood cancer prior to 21 years of age
- Treated with > 20 Gy of chest radiation (mantle, mediastinal, lung, or chest)
- Age 25-49 years at time of enrollment into the study
- Interval from chest radiation to the time of enrollment of > 8 years
- No mammogram or other breast imaging study in the 24 months prior to enrollment
- English-speaking - The University of Colorado AMC Denver and MSKCC group are not
capable of or equipped for conducting a brief motivational interviews by telephone in
another language.
Exclusion Criteria:
- Diagnosed with breast cancer
- Participated in the Project VISION feasibility study (exposed to part of the
intervention)
Type of Study:
Interventional
Study Design:
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
Outcome Measure:
efficacy
Outcome Description:
Determine the efficacy of an intervention, consisting of mailed tailored print materials followed by a telephone-delivered Brief Motivational Interview, on mammogram screening rates compared with an attention control. Mammogram completed by 12-month questionnaire (confirmed by medical record)
Outcome Time Frame:
12 months
Safety Issue:
No
Principal Investigator
Kevin C Oeffinger, MD
Investigator Role:
Principal Investigator
Investigator Affiliation:
Memorial Sloan-Kettering Cancer Center
Authority:
United States: Institutional Review Board
Study ID:
10-104
NCT ID:
NCT01579552
Start Date:
July 2010
Completion Date:
July 2014
Related Keywords:
- Cancer
- Questionnaires
- telephone counseling session
- 10-104
- Childhood Cancer Survivor Women Post Chest Radiation
- Breast Neoplasms
Name | Location |
St. Jude Children's Research Hospital |
Memphis, Tennessee 38105-2794 |