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Blood Test (Guardant Shield™) for Screening of Colorectal Cancer in Underserved Patients

The Ohio State University Guardant Shield™ Colorectal Cancer Screening Project

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05716477
Enrollment
146
Registered
2023-02-08
Start date
2022-12-23
Completion date
2024-11-30
Last updated
2025-01-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Carcinoma

Brief summary

This clinical trial evaluates the use of a blood test (Guardant Shield™) for colorectal cancer screening. Colorectal cancer is the third leading cancer and cause of death in the United States. Screening may help doctors find colorectal cancer early when it is easier to treat yet nearly a third of all people eligible for screening have never had a screening test performed. Currently, doctors use a stool- based test such as the fecal immunochemical test (FIT) and visual tests such as a colonoscopy. Blood based testing such as Guardant Shield™, may provide a quick and effective way to screen patients that are hard to reach or with limited access (underserved).

Detailed description

PRIMARY OBJECTIVES: I. Recruit women age 45 years and older who are in need of colorectal cancer screening from minority and underserved populations via a community mammography van. II. Obtain data regarding knowledge, attitudes and beliefs about colorectal cancer screening. OUTLINE: Participants undergo blood specimen collection and complete survey on study. Participants may optionally undergo standard of care FIT testing on study.

Interventions

PROCEDUREBiospecimen Collection

Undergo blood sample collection

OTHERSurvey Administration

Complete survey

Sponsors

Guardant Health, Inc.
CollaboratorINDUSTRY
Ohio State University Comprehensive Cancer Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
45 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Women aged 45 years of age and older who are in need of colorectal screening * Do not have a history of cancer * Able to read and understand English * Have a provider to receive the results of the test and who will follow-up test results * Able to provide informed consent

Design outcomes

Primary

MeasureTime frameDescription
Number of patients consentedUp to 2 yearsThe number and percentage of patients consented out of those approached to be summarized.
Percentage of patients consentedUp to 2 yearsThe number and percentage of patients consented out of those approached to be summarized.
Knowledge about colorectal screeningUp to 2 yearsSummary statistics and data graphics (boxplots, scatterplots, lattice plots) will summarize data about colorectal screening from overall sample and will be correlated with patient demographics using appropriate statistical tests depending on the nature of the data (correlations, t-tests, chi-squared tests, etc.).
Attitudes about colorectal screeningUp to 2 yearsSummary statistics and data graphics (boxplots, scatterplots, lattice plots) will summarize data about colorectal screening from overall sample and will be correlated with patient demographics using appropriate statistical tests depending on the nature of the data (correlations, t-tests, chi-squared tests, etc.).
Beliefs about colorectal screeningUp to 2 yearsSummary statistics and data graphics (boxplots, scatterplots, lattice plots) will summarize data about colorectal screening from overall sample and will be correlated with patient demographics using appropriate statistical tests depending on the nature of the data (correlations, t-tests, chi-squared tests, etc.).

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026