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A Smartphone-Based Intervention to Improve Colorectal Cancer Screening in African American Men

I

ISA Associates, Inc.

Status

Completed

Conditions

Colorectal Cancer

Treatments

Behavioral: Control
Behavioral: CRC mHealth

Study type

Interventional

Funder types

Other

Identifiers

NCT06052202
R44CA246899

Details and patient eligibility

About

The goal of this clinical trial is to test a new smartphone-based program designed to help African American men get screened for colorectal cancer (CRC). The main question it aims to answer is:

° Are African American men who complete the smartphone-based program more likely to get screened for colorectal cancer than men who do not?

Participants will:

  • Complete a baseline survey asking about their colorectal cancer screening history and their thoughts and beliefs about colorectal cancer and the medical system.
  • Be randomized to receive the new smartphone-based program or to receive text messages containing colorectal cancer education materials designed by the Centers for Disease Control (CDC). The new program sends text messages with information about colorectal cancer. Some of these text messages have links to videos that try to help men overcome anything that may stand in the way of getting screened.
  • Complete a follow-up survey 6 months after the baseline survey. This survey will ask the same questions as the baseline survey.
  • A medical records review will be conducted at 6 months to verify whether participants received a colorectal cancer screening test during the study period.

Researchers will compare participants who receive the new smartphone-based program to participants who receive the CDC information. The goal is to see whether the smartphone-based program increasing screening more than standard educational materials available on the internet.

Enrollment

128 patients

Sex

Male

Ages

45 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • African American/Black
  • not compliant with current United States Preventive Services Taskforce colorectal cancer screening recommendations
  • owns a mobile phone capable of text messaging and accessing webpages
  • able to speak/understand English

Exclusion criteria

  • personal history of colorectal cancer

Trial design

Primary purpose

Screening

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

128 participants in 2 patient groups

CRC mHealth intervention
Experimental group
Description:
Experimental group participants will have access to the CRC mHealth intervention.
Treatment:
Behavioral: CRC mHealth
Control Education
Active Comparator group
Description:
Control condition participants will receive information about colorectal cancer and screening developed by the Centers for Disease Control.
Treatment:
Behavioral: Control

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Douglas Billings, Ph.D.; Samantha L Leaf, Ph.D.

Data sourced from clinicaltrials.gov

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