The Cancer Stage Shifting Initiative: Registry and Biorepository to Research and Address Health Disparities in Cancer Care
National Minority Quality Forum
Summary
The goal of this observational study is to establish a patient registry and a biorepository (sample collection and storage) to investigate health disparities, access, and barriers to cancer screening and early detection technologies. The registry and biorepository will serve as a resource to support Cancer Early Detection (CED) screenings and future research focused on communities at increased risk for cancer. The study seeks to address: •Barriers and disparities in cancer prevention, screening, and treatment, particularly in historically underrepresented populations. Participants will: * Attend a minimum of five clinic visits over a five-year period for scheduled annual assessments while actively enrolled in the study. * Complete questionnaires at each visit that collect information on their medical history, cancer history, and family cancer history. * Allow relevant health information from their electronic health records (EHR) to be collected and reviewed. * Provide blood, saliva, and stool samples for research purposes. * Enter a long-term follow-up period for an additional five years.
Eligibility
- Age range
- 35+ years
- Sex
- All
- Healthy volunteers
- Yes
Registry Inclusion Criteria: 1. Adults 35 years and older. 2. Participant provides written informed consent prior to initiation of any study procedures. 3. Participant understands the purpose and procedures of the study. 4. Participant agrees that demographic data, medical history, and social determinants of health on the enrollment questionnaires can be used for research purposes. 5. Participant agrees to the release and review of their electronic medical record. 6. Participant agrees to be followed for the duration outlined in this protocol. Biorepository 1. Participant is able, in the i…
Locations (2)
- Life in 3D Health ServicesFlint, Michigan
- Grace ClinicHouston, Texas