Informed Choice - Compass

NCT05246839 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 1823

Last updated 2025-11-10

No results posted yet for this study

Summary

The primary objective of this study is to evaluate the impact of a theoretically grounded video that includes information about CRC screening modality choices on CRC screening rates and time adherent to CRC guidelines. The results will not be posted because the study terminated early and the primary endpoint was not analyzed.

Conditions

Interventions

BEHAVIORAL

Brief Video

Videos about colorectal cancer screening.

BEHAVIORAL

Brief Video Plus

Videos about colorectal cancer screening and modalities.

Sponsors & Collaborators

  • Mayo Clinic

    collaborator OTHER
  • University of Utah

    collaborator OTHER
  • American Cancer Society, Inc.

    collaborator OTHER
  • F!ght Colorectal Cancer

    collaborator UNKNOWN
  • Exact Sciences Corporation

    lead INDUSTRY

Principal Investigators

  • Joan M. Griffin, PhD · Mayo Clinic College of Medicine

  • John Inadomi, MD · University of Utah

  • Charles R. Rogers, PhD · Rogers Solutions Group

Eligibility

Min Age
45 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-04-28
Primary Completion
2025-01-31
Completion
2025-01-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05246839 on ClinicalTrials.gov