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Recruiting NCT07361614

Pilot Testing of a Colorectal Cancer Education Program

No phase Interventional Colorectal Cancer Screening

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Educational Program.
Who it may be relevant to
Registry conditions: Colorectal Cancer Screening. Basic parameters: 45 years — 75 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

The primary objective of this study is to assess the feasibility, acceptability, and preliminary efficacy of a culturally and linguistically targeted, colorectal cancer (CRC) education program to improve CRC screening completion.

Interventions

  • Behavioral Educational Program
    Culturally and linguistically tailored program consisting of community health worker (CHW)-led education sessions followed by patient navigation (PN) services.

Primary outcome measures

  • CRC screening completion (yes/no) [Time frame: Month 6]
Secondary outcome measures (4)
  • Change in Brief Illness Perception Questionnaire (IPQ-B) score [Time frame: Baseline, Month 6]
  • Change in Medicines Questionnaire (BMQ) score [Time frame: Baseline, Month 6]
  • Change in number of barriers to care [Time frame: Baseline, Month 6]
  • Change in trust in health/community health workers [Time frame: Baseline, Month 6]

Eligibility criteria

Inclusion criteria

  • Age 45-75 years
  • Not guideline concordant (no stool testing for CRC within past 1 year)
  • No colonoscopy in past 10 years; no sigmoidoscopy or CT colonography in past 5 years)
  • Understands English or Chinese languages.
  • Willing and able to consent to participate

Exclusion criteria

1\) history of CRC or colectomy

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Prevention

Study locations

United States · 1 center
  • NYU Langone Health — New York

Identifiers

NCT: NCT07361614 · 25-01040 · K01CA255411

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗