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Increasing Access to Colorectal Cancer Testing (IACCT) for Blacks

Increasing Access to Colorectal Cancer Testing (IACCT) for Blacks

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03078348
Acronym
IACCT
Enrollment
331
Registered
2017-03-13
Start date
2011-12-05
Completion date
2017-05-03
Last updated
2022-11-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Cancer, Colorectal Carcinoma

Keywords

cancer screening

Brief summary

The purpose of this research study is to compare a new educational material to another widely available educational brochure. The goal is to see if the new educational material will change knowledge and behaviors about colorectal cancer and colorectal screening.

Interventions

OTHERFecal Immunochemical Test (FIT) Kit

Free FIT Kits distributed at study entry.

BEHAVIORALCulturally targeted Photo Novella Booklet

Culturally targeted Photo Novella Booklet + culturally targeted reminders. Print materials developed by the Centers for Disease Control and Prevention (CDC)) to provide information about CRC, importance of screening and available screening tests. Timed reminder letters and/or emails intended as a cue to action and as educational boost to facilitate participant screening decision making and screening uptake.

BEHAVIORALScreen for Life Brochure

Screen for Life Brochure + standard reminders. Print materials developed by the Centers for Disease Control and Prevention (CDC)) to provide information about CRC, importance of screening and available screening tests. Timed reminder letters and/or emails intended as a cue to action and as educational boost to facilitate participant screening decision making and screening uptake.

Sponsors

American Cancer Society, Inc.
CollaboratorOTHER
H. Lee Moffitt Cancer Center and Research Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
NONE

Intervention model description

In this modified block random assignment, all individuals recruited from the same geographic unit will receive the intervention assigned to that area in order to reduce intervention contamination. Individuals will not be made aware of their randomization (intervention) condition until after baseline assessment. The research assistants will also be assigned at random to work with one geographic area (i.e., one intervention condition) in order to reduce risk of intervention contamination by study staff.

Eligibility

Sex/Gender
ALL
Age
50 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Community-based recruitment methods will be used including promotional flyers and word of mouth at locations such as churches, barber shops, civic/community social service centers, senior centers, cultural groups. The flyers will provide brief information and advertise a telephone number for potential participants to call the study office at Moffitt. * Self identify as Black or African American * Have no symptoms of colorectal cancer (CRC), or personal diagnosis of CRC or bowel inflammatory disease or related syndromes * Have not had recent CRC screening per guidelines (never screened or overdue) * Participants must provide at least two forms of contact information (mailing address, home telephone or cell phone or email address), and contact information of a secondary individual who has a number that is different from the participant (this person may be a relative or friend living with the respondent). * Spouse or relatives of respondent are potentially eligible.

Exclusion criteria

* Individuals who have participated in a colorectal cancer screening (CRCS) research in the past 1 year will not be eligible for this study. * Additional criteria may apply.

Design outcomes

Primary

MeasureTime frameDescription
Rate of Fecal Immunochemical Test (FIT) Kit Return Per Study Arm6 months post final enrollmentFit screening uptake at 6 months. Number of participants who used and returned their FIT Kit, per study arm. A FIT Kit was provided to participants in both study arms for use and return.

Secondary

MeasureTime frameDescription
Rate of Diagnostic ColonoscopyPost 6 month follow-upNumber of participants who participated in a diagnostic colonoscopy, post test kit return.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026