A Patient-centered Intervention Using Technology to Reduce Colorectal Cancer Disparities in Primary Care

  • STATUS
    Recruiting
  • days left to enroll
    66
  • participants needed
    4000
  • sponsor
    University of Florida
Updated on 15 March 2022
Accepts healthy volunteers

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

Description

Patients (N=3,000) 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.

Details
Condition Colo-rectal Cancer
Treatment virtual technology - highly tailored, virtual technology - tailored minimally
Clinical Study IdentifierNCT03407417
SponsorUniversity of Florida
Last Modified on15 March 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

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

Exclusion Criteria

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
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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