Colorectal Cancer Screening Outreach

Part of paid clinical trials in New Haven, Connecticut.

Sponsor
Yale University
Study ID
NCT07345676
Status
Recruiting
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Conditions

  • Colo-rectal Cancer

Eligibility Criteria

Sex
ALL
Age
45 Years - 75 Years
Healthy Volunteers
Not accepted

Interventions

  • Bundled messaging intervention — BEHAVIORAL
    A bundled intervention of text message, letter, and provider reminder. Text message content using behaviorally motivated messages will vary.

Study Details

This is a 4 arm pragmatic trial to test a multicomponent intervention designed to improve adherence to colorectal cancer screening.

Key Dates

First listed
Jan 16, 2026
Start date
Jun 23, 2026
Status verified
Jul 2026
Primary completion
Apr 30, 2027
Completion
Jul 31, 2027

Study Design

Enrollment
2,000 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING

Arms

  • No Intervention: Control-Usual Care
    Participants will receive a simple text message reminder
  • Experimental: Messaging Group A
    Participants will receive a series of outreach messages including texts with two-way messaging capabilities, mailed letter, and a reminder to their clinician. Content of the text message arm will be varied so that patients receive one of three messages (A, B or C).
  • Experimental: Messaging Group B
    Participants will receive a series of outreach messages including texts with two-way messaging capabilities, mailed letter, and a reminder to their clinician. Content of the text message arm will be varied so that patients receive one of three messages (A, B or C).
  • Experimental: Messaging Group C
    Participants will receive a series of outreach messages including texts with two-way messaging capabilities, mailed letter, and a reminder to their clinician. Content of the text message arm will be varied so that patients receive one of three messages (A, B or C).

Primary Outcome Measure

Number of participants with scheduled or completed colorectal cancer screening. [ Time Frame: up to 3 months from randomization ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Cornell Scott Hill HealthNew HavenConnecticut06519-

Find similar trials in New Haven, CT

By research site
Cornell Scott Hill Health· New Haven, CT

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