Clinical trial Recruiting at 2 sites Interventional Ages 18 and up

Helping colorectal cancer survivors keep up with post-surgery surveillance

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

Run by Fred Hutchinson Cancer Center · NCT06995924 · Data updated 2026-11-12

This project tests whether patient navigation services, an interactive web program called Current Together After Cancer (CTAC), or both help people with stage I–III colorectal cancer keep up with recommended post-surgery surveillance.

More Stage III Colorectal Cancer AJCC v8 trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment75 (estimated)
SponsorFred Hutchinson Cancer Center
Academic / other
Locations2 sites (Seattle, Washington and 1 other locations)
StatusRecruiting
StartedNovember 17, 2025
Main results expectedMarch 31, 2027
Study endsMarch 31, 2027
Registry record updatedSeptember 1, 2026
Trial IDNCT06995924 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (age ≥18) with stage I–III colorectal cancer who are within three months of standard surgical resection and receive care at a participating clinic and can complete surveys in English.

Probably not a fit

Patients who are treated outside the participating Seattle clinics, are more than three months post-surgery, are under 18, or cannot complete English surveys are unlikely to benefit from this program.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This pilot assigns patients to one of three arms based on the clinic where they receive care: navigation only, CTAC web education only, or both navigation and CTAC. Navigation includes education about surveillance, reminders, and scheduling assistance, while CTAC provides self-directed interactive web education and a checklist of recommended tests. Participants are enrolled within three months of surgical resection and followed at about 3 months after enrollment and again 12–18 months after surgery to measure receipt of recommended laboratory tests, imaging, and endoscopy. The trial tests whether these supports increase adherence to guideline-recommended surveillance in stage I–III colorectal cancer survivors.

Why it matters

Potential benefit: If successful, this approach could increase the number of colorectal cancer survivors who get timely surveillance tests and enable earlier detection of recurrence.

How similar studies have gone: Previous work in cancer care and chronic disease has shown that navigation and web-based education can improve follow-up and screening adherence, though results have been mixed and the combined approach for colorectal cancer surveillance is not yet well established.

Who can join: the full rules

Show full inclusion / exclusion 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

Where it's running

  • Benaroya Research Institute at Virginia Mason
    Seattle, Washington, United States
    Recruiting
  • Fred Hutch/University of Washington Cancer Consortium
    Seattle, Washington, United States
    Recruiting

Study contacts

  • Principal investigator: Rachel B. Issaka, MD, MAS — Fred Hutch/University of Washington Cancer Consortium
  • Study coordinator: Ari Bell-Brown
  • Email: abellbro@fredhutch.org
  • Phone: 206.667.7624

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.