Barriers to Screening Breast MRI Utilization Among Patients at Elevated Risk
- Conditions
- Breast Cancer
- Interventions
- Behavioral: Qualitative InterviewsBehavioral: Self-Report Survey
- Registration Number
- NCT04257474
- Brief Summary
This study seeks to develop an explanatory framework for breast MRI utilization to inform future interventions. The Health Services Utilization Model (HSUM) will guide the selection of specific participant-level factors for examination, including predisposing characteristics (knowledge, health/cultural beliefs), enabling resources (social support, cost/insurance coverage), and perceived need (perceived susceptibility, provider recommendation).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 265
- Ability to speak/read English
- Within 2 years of last screening mammogram
- Pathogenic BRCA1/2 mutations OR estimated lifetime risk ≥20% per the National Cancer Institute (NCI) Breast Cancer Risk Assessment Tool (BCRAT)
- Women who have received a prior diagnosis of breast cancer
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Qualitative Interviews Qualitative Interviews Researchers will randomly select 30 participants from group 1 and will use semi-structured qualitive interviews exploring factors impacting utilization of screening breast MRI Assessing Health Services Utilization Model (HSUM) Self-Report Survey 150 women with a high lifetime breast cancer risk will be recruited from mammography and primary care clinics. Researchers will assess HSUM factors influencing screening breast MRI utilization. Results will identify participant-level HSUM factors significantly associated with screening outcomes.
- Primary Outcome Measures
Name Time Method Reporting Receipt of MRI Breast Screening at Any Time Baseline Participant-reported receipt of screening breast MRI at any time in the past.
Reporting Receipt of MRI Breast Screening in the Last 24 Months Baseline Participant-reported receipt of screening breast MRI in the last 24 months
- Secondary Outcome Measures
Name Time Method Reporting Receipt of Mammogram Baseline Participant-reported receipt of breast cancer screening mammogram in the last 24 months
Reporting Receipt of Chemoprevention Baseline Participant-reported receipt of chemoprevention at any point in time (including currently receiving).
Reporting Receipt of Genetic Testing Baseline Participant-reported receipt of genetic testing at any time in the past
Reporting Receipt of Genetic Counseling Baseline Participant-reported receipt of genetic counseling at any time in the past
Reporting Receipt of Ultrasound Baseline Participant-reported receipt of breast cancer screening ultrasound in the last 24 months
Trial Locations
- Locations (2)
Moffitt Cancer Center
🇺🇸Tampa, Florida, United States
Georgetown Lombardi Comprehensive Cancer Center
🇺🇸Washington, District of Columbia, United States