A Patient-centered Intervention Using Technology to Reduce Colorectal Cancer Disparities in Primary Care
- Conditions
- Colo-rectal Cancer
- Interventions
- Other: virtual technology - tailored minimallyOther: virtual technology - highly tailored
- Registration Number
- NCT03407417
- Lead Sponsor
- University of Florida
- Brief Summary
The purpose of this proposal is to test the efficacy of a patient-centered, tailored message intervention delivered via virtual technology for increasing colorectal cancer (CRC) screening within guidelines among racial/ethnic minority and rural patients. This protocol focuses on the clinical portion of grant NCI 1RCA207689-01A1
- Detailed Description
Patients will be recruited via a secure, clinical data warehouse to complete a patient-randomized test of the efficacy of the intervention for promoting initial and repeat FIT testing. Patients identified as eligible will be contacted through MyChart to test a web-based, culturally-sensitive virtual human intervention for CRC screening. The web-application will provide information to encourage CRC screening. Therefore, this study is a minimal risk study.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 960
- able to read English or Spanish at least at eighth-grade level
- have an email account or the ability to receive texts
- willingness to be re-contacted
- consent to MRR related to CRC screening
- not remember completing any CRC screening within recommended guidelines (i.e., <10 years for colonoscopy, <1 year for stool test).
- complete a FIT test:
- a) with a negative result only
- b) complete a FIT test with a positive result AND undergo a completion screening colonoscopy,
- Or c) complete a colonoscopy only.
- unable to read English at least at eighth-grade level
- doesn't have an email account or the ability to receive texts
- unwilling to be re-contacted
- Unable to consent to MRR related to CRC screening
- have not had <10 years for colonoscopy, or 1 year for stool test
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Non-FIT testing virtual technology - tailored minimally Patients who elected not to have FIT testing after interaction with the application Fit Testing virtual technology - highly tailored Patients who self selected to receive FIT screening after interaction with the Application
- Primary Outcome Measures
Name Time Method Intention to Screen for Colorectal Cancer (CRC) within the first 12 months Measure: Intention to Screen for Colorectal Cancer Item: I want to get screened for colorectal cancer. Scale: 5-point Likert scale (1 = strongly disagree to 5 = strongly agree). Mean scores near 1 indicate a lower intention to get screened for colorectal cancer. Mean scores near 5 indicate a higher intention to get screened for colorectal cancer.
Construct: Behavioral intention to screen No subscales
- Secondary Outcome Measures
Name Time Method Communication With a Provider About Colorectal Cancer (CRC) Assessed after 24 months Measure: Intention to talk to doctor about colorectal cancer screening. Construct: Behavioral intention to communicate Item: I will talk to my healthcare provider about colorectal cancer screening. Scale: 5-point Likert scale (1 = strongly disagree to 5 = strongly agree). Mean scores near 1 indicate a lower intention to talk to a healthcare professional about colorectal cancer screening. Mean scores near 5 indicate a high intention to talk to a healthcare professional about colorectal cancer screening.
No subscales
Trial Locations
- Locations (1)
University of Florida
🇺🇸Jacksonville, Florida, United States