Increasing CRC Screening in Community Health Centers Through Mobile Messaging Optimization

NCT07569250 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 7220

Last updated 2026-05-06

No results posted yet for this study

Summary

The goal of this interventional study is to create and test a comprehensive and low burden text message program within existing Community Health Centers (CHC) electronic records system to encourage patients to complete at home colorectal cancer (CRC) screening and to make sure they get follow-up care if their results are abnormal.

First, we will learn from clinic staff and patients what their needs and preferences are in terms of use of technology. We will use this information to design the text messages program.

* Clinic patients will participate in focus groups
* Clinic staff will participate in interviews

Second, we will test a series of different message versions in two batches (experiments):

* Clinic patients with orders for an at-home colorectal cancer screening kit will receive the different message versions.
* In the first batch, the messages that get the most engagement from patients will be selected to be used in the second experiment.
* In the second batch, we will test which messages lead to the most colorectal cancer screening completion.
* This will be rolled-out within the clinics existing electronic record system. The study team will not receive any information that will identify individual patients.

Lastly, we will check again with clinic staff to learn how the program performed, and what would be needed to continue using the text message program in the long run.

-Clinic staff will participate in interviews and surveys.

Conditions

Interventions

BEHAVIORAL

Personalized Text Message

Message includes personalized content.

BEHAVIORAL

Screening Concerns Text Message

Emotional concerns or barriers related to CRC screening.

BEHAVIORAL

Message Framing Text Message

Use gain-framed language to influence motivation.

BEHAVIORAL

Autonomy Support Outreach

Provide patients with choices or options to increase sense of control.

BEHAVIORAL

Impediments Support Outreach

Include information or resources to help overcome barriers to care.

BEHAVIORAL

Live Support Outreach

Offer access to live assistance.

OTHER

Data Reporting and Visualization System Tools

Electronic alerts, dashboards, and tracking systems used to identify and follow up with patients due for CRC screening or abnormal results.

Sponsors & Collaborators

  • National Institutes of Health (NIH)

    collaborator NIH
  • National Cancer Institute (NCI)

    collaborator NIH
  • Massachusetts League of Community Health Centers

    collaborator OTHER
  • Dana-Farber Cancer Institute

    collaborator OTHER
  • University of Texas Southwestern Medical Center

    collaborator OTHER
  • Massachusetts General Hospital

    collaborator OTHER
  • University of Colorado, Denver

    lead OTHER

Principal Investigators

  • Gina Kruse, MD · University of Colorado, Denver

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
FACTORIAL

Eligibility

Min Age
45 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-12-31
Primary Completion
2031-10-31
Completion
2032-01-31

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07569250 on ClinicalTrials.gov