Narrative or Fact-Based Videos in Increasing Colorectal Cancer Screenings in African American Communities

Roswell Park Comprehensive Cancer Center

Status: Completed

Conditions: Healthy, no Evidence of Disease; Colorectal Cancer

Treatments: Behavioral: behavioral intervention

Study type: Interventional

Funder types: Other

Identifiers

NCT02100254

NCI-2013-01707 (Registry Identifier)

I 159309 (Other Identifier)

Details and patient eligibility

About

This randomized clinical trial studies narrative or fact-based videos in increasing colorectal cancer screenings in African American communities. Informational videotapes may help increase the number of participants who engage in colonoscopy screenings. It is not yet known whether narrative videos may be more effective than fact-based videos in increasing colorectal cancer screenings.

Full description

PRIMARY OBJECTIVES:

I. Assess both individual and environmental factors that guide decisions and behaviors to engage or not engage in colonoscopy screenings for African Americans in the two communities.

II. Using a Community-Based Participatory Research (CBPR) approach, develop and pilot a peer-led, narrative-based colorectal cancer behavioral intervention for increasing colonoscopy screening behaviors in African Americans.

III. Examine the efficacy of a narrative communication-style group intervention compared to a didactic intervention to influence African Americans' engagement in colorectal cancer screening, including examining the degree to which the community interventions impact cognitive and affective decision making factors about health care seeking.

IV. Examine and explore contextual factors that may influence the process of behavior change to better understand colorectal cancer (CRC) screening and health care seeking behaviors.

OUTLINE: Program locations are randomized to 1 of 2 arms.

ARM I: Participants view videos with information about CRC and screening delivered by personal narrative.

ARM II: Participants view videos with information about CRC and screening delivered by informative fact-based message.

After completion of study, patients are followed up at 3 and 6 months.

Enrollment: 1,310 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Participants in each component (focus groups, surveys and educational programs) will be 18 years of age and over; these men and women are generally healthy, ambulatory and able to participate in events in their community; no women, men, or children of any ethnic or social background will be excluded from the educational program
• EDUCATIONAL INTERVENTION:
• Currently non-adherent to colorectal cancer screening
• Self-identify as African American
• Are 50 years of age or older
• Have the ability to provide informed consent in English
• FOLLOW-UP ASSESSMENTS:
• Must be non-adherent for CRC screening at the time of the educational program
• Have telephone service (mobile or landline), to participate in the follow up interviews
• Agree to providing consent for release/review of their medical record

Exclusion criteria

• Non-English speaking

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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1,310 participants in 2 patient groups

Arm I (personal narrative)

Experimental group

Description:

Participants view videos with information about CRC and screening delivered by personal narrative.

Treatment:

Behavioral: behavioral intervention

Behavioral: behavioral intervention

Arm II (fact-based message)

Active Comparator group

Description:

Participants view videos with information about CRC and screening delivered by informative fact-based message.

Treatment:

Behavioral: behavioral intervention

Behavioral: behavioral intervention