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A Multilevel Intervention to Increase Colorectal Cancer Screening Tests in Patients With Abnormal Fecal Immunochemical Test Results, PROACT Trial

Fred Hutchinson Cancer Center (FHCC) logo

Fred Hutchinson Cancer Center (FHCC)

Status

Invitation-only

Conditions

Colorectal Carcinoma

Treatments

Other: Interview
Other: Educational Intervention
Other: Best Practice
Other: Supportive Care
Other: Survey Administration
Other: Electronic Health Record Review

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06822530
R37CA295618 (U.S. NIH Grant/Contract)
RG1124701
NCI-2024-08639 (Registry Identifier)
FHIRB0020712 (Other Identifier)

Details and patient eligibility

About

This clinical trial studies whether an intervention that addresses two or more levels of care (multilevel intervention) increases follow-up of abnormal, non-invasive, colorectal cancer (CRC) screening test results. The fecal immunochemical test (FIT) is a non-invasive, stool-based, CRC screening test. FITs are relatively inexpensive and can be completed at home, for these reasons, it is a preferred method of CRC screening in healthcare settings that care for under-resourced patients or have limited colonoscopy access. For FIT-based CRC screening to be effective, abnormal results must be followed by a colonoscopy, however many patients fail to complete this recommended follow-up test. The multilevel intervention addresses barriers to follow-up colonoscopy at the patient and health system levels of care through a CRC screening patient navigator, an educational video, and transportation assistance. The navigator provides patient support and assistance with colonoscopy scheduling. The educational video addresses identified patient fears around colonoscopies. Transportation assistance is offered after the colonoscopy through a rideshare program to address transportation barriers. Therefore, this multilevel intervention may increase follow-up colonoscopy completion in patients with abnormal FIT results.

Full description

OUTLINE: Patients are randomized to 1 of 2 groups.

GROUP I: Patients receive usual care from the CRC screening program navigator which includes monthly phone calls with the CRC screening program navigator, and assistance with colonoscopy scheduling.

GROUP II: Patients receive usual care as described in Group I and additionally receive a quick response (QR) code with a link to a video to address patient-level fears of colonoscopy screening via text message, mailed letter, or EHR platform as well as access to transportation home after colonoscopy via a rideshare program arranged through the discharge nurse.

After completion of study intervention, patients are followed up for 18 months.

Enrollment

682 estimated patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • PATIENTS: Age >= 45 years old and =< 75 years old
  • PATIENTS: Receives care at an Harborview Medical Center (HMC) or University of Washington-Kent-Des Moines (UW-KDM) primary care clinic
  • PATIENTS: >= 1 month from documented abnormal FIT result
  • PATIENTS: Has not received a colonoscopy between the abnormal FIT and enrollment
  • CLINIC STAFF: HMC or UW-KDM physician or staff member who provides primary care or gastroenterology care
  • CLINIC STAFF: Staff in the Fred Hutchinson (Fred Hutch)/UW Medicine Population Health Program that provide colorectal cancer screening and navigation

Trial design

Primary purpose

Screening

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

682 participants in 2 patient groups

Group I (usual care)
Active Comparator group
Description:
Patients receive usual care from the CRC screening program navigator which includes monthly phone calls with the CRC screening program navigator, and assistance with colonoscopy scheduling.
Treatment:
Other: Electronic Health Record Review
Other: Best Practice
Group II (usual care, video, rideshare transportation)
Experimental group
Description:
Patients receive usual care as described in Group I and additionally receive a QR code with a link to a video to address patient-level fears of colonoscopy screening via text message, mailed letter, or EHR platform as well as access to transportation home after colonoscopy via a rideshare program arranged through the discharge nurse on study.
Treatment:
Other: Electronic Health Record Review
Other: Survey Administration
Other: Supportive Care
Other: Educational Intervention
Other: Best Practice
Other: Interview

Trial contacts and locations

1

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Central trial contact

Rachel B. Issaka, MD, MAS

Data sourced from clinicaltrials.gov

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