RecruitingRecruiting
Improving Uptake of Surveillance in Colorectal Cancer Survivors Through Navigation and Web Education
NCT06995924 · Fred Hutchinson Cancer Center
In plain English
Click the button to translate this study into plain language — what it is, who qualifies, and what participation looks like.
Official title
A Pilot Trial to Evaluate the Effectiveness of Navigation, Interactive Web Education, or the Combination of Both to Promote Guideline-Concordant Colorectal Cancer Surveillance Care
About this study
OUTLINE:
Patients are assigned to 1 of 3 arms based on the clinic location they receive cancer care at.
ARM A (VIRGINIA MASON): Patients receive access to navigation services, including education on surveillance care, reminders to complete care and assistance in scheduling surveillance, within 3 months of standard of care surgical resection for stage I-III CRC.
ARM B (FRED HUTCH \[SOUTH LAKE UNION\]): Patients receive access to the CTAC intervention, which includes self-directed, interactive web-based education about surveillance and a checklist of care, within 3 months of standard of care surgical resection for stage I-III CRC.
ARM C (FRED HUTCH \[OVERLAKE + EVERGREEN\]): Patients receive access to navigation services, including education on surveillance care, reminders to complete care and assistance in scheduling surveillance, and access to the CTAC intervention, which includes self-directed, interactive web-based education about surveillance and a checklist of care, within 3 months of standard of care surgical resection for stage I-III CRC.
Patients are followed up at 3 months post study-enrollment and 12-18 months after surgical resection.
Eligibility criteria
Inclusion Criteria:
* Age ≥ 18 due to disease and clinic population
* Stage I-III CRC survivor within 3 months post-surgical resection
* Being seen at a participating clinic
* Ability to understand and complete surveys in English
Study design
Enrollment target: 75 participants
Allocation: non_randomized
Masking: none
Age groups: adult, older_adult
Timeline
Starts: 2025-11-17
Estimated completion: 2027-03-31
Last updated: 2026-02-20
Interventions
Other: Educational InterventionOther: Electronic Health Record ReviewOther: Internet-Based InterventionBehavioral: Patient NavigationOther: Survey Administration
Primary outcomes
- • Completion of colonoscopy (stage I colorectal carcinoma patients) (Up to 18 months post-surgical resection)
- • Completing any colonoscopy, carcinoembryonic antigen tumor marker (CEA), and cross-sectional imaging (stage II-III colorectal carcinoma patients) (Up to 18 months post-surgical resection)
Sponsor
Fred Hutchinson Cancer Center · other
Contacts & investigators
ContactAri Bell-Brown · contact · abellbro@fredhutch.org · 206.667.7624
InvestigatorRachel B. Issaka, MD, MAS · principal_investigator, Fred Hutch/University of Washington Cancer Consortium
All locations (2)
Benaroya Research Institute at Virginia MasonRecruiting
Seattle, Washington, United States
Fred Hutch/University of Washington Cancer ConsortiumRecruiting
Seattle, Washington, United States