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Recruiting NCT05174286

NCT05174286 Community Health Workers United to Reduce Colorectal Cancer and Cardiovascular Disease Among People at Higher Risk

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Clinical Trial Summary
NCT ID NCT05174286
Status Recruiting
Phase
Sponsor Columbia University
Condition Colorectal Cancer
Study Type INTERVENTIONAL
Enrollment 880 participants
Start Date 2023-03-19
Primary Completion 2026-06-30

Eligibility & Interventions

Sex All sexes
Min Age 45 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
SBIRTReferral as Usual (RAU)

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 880 participants in total. It began in 2023-03-19 with a primary completion date of 2026-06-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The overall goal of this study is to develop a comprehensive, culturally tailored community-based colorectal cancer (CRC) prevention model with a dual emphasis on reducing CRC risk along with its CVD risk factors. The study intervention has two components: Screening, Brief Intervention, and Referral to Treatment (SBIRT) to address CRC screening and a web-based lifestyle program called "Alive!" to address CVD risk factors linked to CRC. The C.H.U.R.C.H. Trial (Community Health workers (CHW) United to Reduce Colorectal cancer and cardiovascular disease among people at Higher risk) has four specific aims: (1) to compare the effect of a CHW-Led SBIRT (Intervention) to Referral As Usual (RAU) (Usual Care) on guideline-concordant CRC screening uptake; (2) to evaluate the effect of a Culturally Adapted CHW-linked Alive! (CACA) program incorporated into the intervention arm on dietary inflammatory score (DIS); (3) to evaluate the effect of CACA on changes in Life Simple-7 (LS7) scores; and (4) to examine the multi-level contextual mechanisms and factors influencing CHW effectiveness, reach, and implementation of CRC screening uptake and CACA activities through a mixed-methods process evaluation. Given the broad reach and influence of churches, results from this study can be used to inform future scale up of this multi-pronged intervention.

Eligibility Criteria

Inclusion Criteria: 1. English-speaking 2. Aged 45 years and older 3. Not up-to-date with CRC 4. Working telephone 5. Can provide informed consent Exclusion Criteria: 1. Non-English speaking 2. \<45 years old

Contact & Investigator

Central Contact

Lisa Matthews, EdD, MPH

✉ lam2160@cumc.columbia.edu

📞 212-853-1150

Principal Investigator

Olajide A. Williams, MD, MS

PRINCIPAL INVESTIGATOR

Columbia University

Frequently Asked Questions

Who can join the NCT05174286 clinical trial?

This trial is open to participants of all sexes, aged 45 Years or older, studying Colorectal Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05174286 currently recruiting?

Yes, NCT05174286 is actively recruiting participants. Contact the research team at lam2160@cumc.columbia.edu for enrollment information.

Where is the NCT05174286 trial being conducted?

This trial is being conducted at New York, United States.

Who is sponsoring the NCT05174286 clinical trial?

NCT05174286 is sponsored by Columbia University. The principal investigator is Olajide A. Williams, MD, MS at Columbia University. The trial plans to enroll 880 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology