Increasing CRC Screening in Community Health Centers Through Mobile Messaging Optimization
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- University of Colorado, Denver
- Study ID
- NCT07569250
- Status
- Not Yet Recruiting
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Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 45 Years - 75 Years
- Healthy Volunteers
- Accepted
Interventions
- Personalized Text Message — BEHAVIORALMessage includes personalized content.
- Screening Concerns Text Message — BEHAVIORALEmotional concerns or barriers related to CRC screening.
- Message Framing Text Message — BEHAVIORALUse gain-framed language to influence motivation.
- Autonomy Support Outreach — BEHAVIORALProvide patients with choices or options to increase sense of control.
- Impediments Support Outreach — BEHAVIORALInclude information or resources to help overcome barriers to care.
- Live Support Outreach — BEHAVIORALOffer access to live assistance.
- Data Reporting and Visualization System Tools — OTHERElectronic alerts, dashboards, and tracking systems used to identify and follow up with patients due for CRC screening or abnormal results.
Study Details
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, the investigators will learn from clinic staff and patients what their needs and preferences are in terms of use of technology. This information will be used to design the text messages program. * Clinic patients will participate in focus groups * Clinic staff will participate in interviews Second, the investigators 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, the investigators 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, the investigators 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.
Key Dates
- Start date
- Dec 31, 2026
- Status verified
- Jun 2026
- Primary completion
- Oct 31, 2031
- Completion
- Jan 31, 2032
Study Design
- Enrollment
- 7,220 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- FACTORIAL
- Primary purpose
- HEALTH_SERVICES_RESEARCH
Arms
- Experimental: Standard Message - Gain FrameNo personalization, no concerns/negative emotion, gain-framed message.
- Experimental: Concern Message - Gain FrameNo personalization, screening concerns/negative emotions, gain-framed message.
- Experimental: Concern Message - No Gain FrameNo personalization, screening concerns/negative emotions, no gain-framed message.
- Experimental: Standard Message - No Gain FrameNo personalization, no screening concerns/negative emotions, no gain-framed message.
- Experimental: Personalized Message - Gain FramePersonalization included, no screening concerns/negative emotions, gain-framed message.
- Experimental: Personalized Message - No Gain FramePersonalization included, no screening concerns/negative emotions, no gain-framed message.
- Experimental: Personalized - Concern Message - Gain FramePersonalization and screening concerns/negative emotions, gain framed message.
- Experimental: Personalized - Concern Message - No Gain FramePersonalization and screening concerns/negative emotions, no gain-framed message.
- Experimental: Basic Outreach OnlyNo autonomy support, no impediments support, no live support.
- Experimental: Outreach + Impediments SupportNo autonomy support, no live support. Impediment support.
- Experimental: Outreach + Impediments + Live SupportNo autonomy support. Impediment support and live support included.
- Experimental: Outreach + Live SupportLive support included. No autonomy or impediments support.
- Experimental: Autonomy Outreach SupportAutonomy support included, no impediments or live support.
- Experimental: Autonomy + Live SupportAutonomy and live support with impediments support.
- Experimental: Autonomy + Impediments SupportAutonomy and impediments support included. No live support included.
- Experimental: Autonomy + Impediments + Live SupportAutonomy, impediments, and live support included.
Primary Outcome Measure
Text message engagement [ Time Frame: 14 days after reminder message delivery ]
Central Contacts
- Yamila Sierra303-724-4811
Locations (4)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Dana Farber Cancer Institute | Boston | Massachusetts | 02215 | Kasisomayajula Viswanath, PhD (SUB_INVESTIGATOR) |
| Massachusetts General Hospital | Boston | Massachusetts | 02114 | Adjoa Anyane-Yeboa, MD, MPH (SUB_INVESTIGATOR) |
| The Massachusetts League of Community Health Center, Inc. | Boston | Massachusetts | 02108 | Susan Dargon-Hart (PRINCIPAL_INVESTIGATOR) |
| University of Texas Southwestern Medical Center | Dallas | Texas | 75390 | Lynn Ibekwe-Agunanna, MPH, PhD (SUB_INVESTIGATOR) |
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