Skip to main content
Clinical Trials/NCT03819920
NCT03819920CompletedNot Applicable

Does Knowing One's Estimated Colorectal Cancer Risk Influence Screening Behavior?

Stanford University1 site in 1 country229 target enrollmentStarted: October 6, 2015Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
229
Locations
1
Primary Endpoint
Screening Behavior: Differences in colorectal cancer screening completion rates between usual care (UC) and CCRAT

Study Overview

Brief Summary

This study is designed to examine the impact of telephone-based colorectal cancer risk assessment on colorectal screening attitudes and behavior among previously unscreened adults ages 50 to 75.

Detailed Description

Colorectal cancer (CRC) remains the 3rd most common cancer in the US. Most CRCs are preventable, but screening participation remains suboptimal. Several factors have been associated with screening compliance, such as perception of CRC risk. Here we study the impact of telephone-based administration of the National Cancer Institute Colorectal Cancer Risk Assessment Tool (CCRAT) compared to usual care.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
50 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Patient of any participating physician
  • •Not having had any colorectal cancer screening test prior
  • •Able to speak English

Exclusion Criteria

  • •Personal history of inflammatory bowel disease
  • •Personal history of colorectal cancer
  • •Personal history of Lynch syndrome or Familial Adenomatous Polyposis
  • •Have already received colorectal cancer screening

Arms & Interventions

Usual Care (UC)

Placebo Comparator

Patients receive standardized general information about colorectal cancer screening over the telephone.

Intervention: Usual Care (UC) (Behavioral)

Risk Assessment (CCRAT)

Active Comparator

Patient receive personalized colorectal cancer risk assessment over the telephone by answering the questions as outlined in the National Cancer Institute Colorectal Cancer Risk Assessment Tool (https://ccrisktool.cancer.gov/calculator.html)

Intervention: Risk Assessment (CCRAT) (Behavioral)

Risk Assessment (CCRAT)

Active Comparator

Patient receive personalized colorectal cancer risk assessment over the telephone by answering the questions as outlined in the National Cancer Institute Colorectal Cancer Risk Assessment Tool (https://ccrisktool.cancer.gov/calculator.html)

Intervention: Usual Care (UC) (Behavioral)

Outcomes

Primary Outcomes

Screening Behavior: Differences in colorectal cancer screening completion rates between usual care (UC) and CCRAT

Time Frame: 12 months after intervention

Any CRC screening test completed including stool tests (FOBT (fecal occult blood test), FIT (immunochemical test for fecal blood), stool DNA test), colonoscopy, flexible sigmoidoscopy, double contrast barium enema, CT colonography (virtual colonoscopy)

Secondary Outcomes

  • Screening Behavior: Differences in colorectal cancer screening completion rates between usual care (UC) and CCRAT(6 months after intervention)
  • Colorectal cancer screening rates at 12 months as a function of CCRAT score(12 months after intervention)
  • Change in intention to screen at 6 months and 12 months(Immediate after intervention, 6 months and 1 year after intervention)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Uri Ladabaum

Professor of Medicine, Director GI Cancer Prevention Program

Stanford University

Study Sites (1)

Loading locations...

Similar Trials