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Audio and Video Brochures for Increasing Colorectal Cancer Screening Among Adults Living in Appalachia

Primary Purpose

Colorectal Carcinoma

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Best Practice
Fecal Immunochemical Test
Health Education
Health Education
Scheduled Notification
Survey Administration
Sponsored by
Ohio State University Comprehensive Cancer Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Colorectal Carcinoma

Eligibility Criteria

50 Years - 64 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Mid-life men and women (50-64 years old) Live in Appalachia Had a medical visit in the past two years Are at average-risk for CRC (no history of CRC, polyps, inflammatory bowel disease, family history of CRC or hereditary CRC syndromes) Are not within CRC screening guidelines (no fecal occult blood test/FIT in the past year; flexible sigmoidoscopy in past five years; colonoscopy in past ten years)

Sites / Locations

  • Ohio State University Comprehensive Cancer Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Experimental

Arm Label

Arm I (FIT, usual care)

Arm II (FIT, audio brochure, reminder)

Arm III (FIT, video brochure, reminder)

Arm Description

Participants receive the FIT kit and usual care on study.

Participants receive the FIT kit with an audio brochure, disposable gloves and stool collection device, and scheduled reminder on study.

Participants receive the FIT kit with a video brochure, disposable gloves and stool collection device, and scheduled reminder on study.

Outcomes

Primary Outcome Measures

Fecal immunochemical test (FIT) return
Will estimate FIT return using proportions for each study group. Both comparisons (each intervention compared to control) will be a two-sample test of proportions (intent-to-treat analysis) using a one-sided alpha of 0.1 due to the preliminary nature of the study. Will estimate critical parameters with point estimates and 95% confidence intervals and provide a preliminary test of effectiveness on FIT completion.

Secondary Outcome Measures

Full Information

First Posted
March 31, 2023
Last Updated
March 31, 2023
Sponsor
Ohio State University Comprehensive Cancer Center
Collaborators
National Institute on Aging (NIA)
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1. Study Identification

Unique Protocol Identification Number
NCT05810714
Brief Title
Audio and Video Brochures for Increasing Colorectal Cancer Screening Among Adults Living in Appalachia
Official Title
Increasing CRC Screening Using Audio and Video Brochures: A Pilot Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Completed
Study Start Date
November 20, 2021 (Actual)
Primary Completion Date
February 1, 2022 (Actual)
Study Completion Date
February 1, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ohio State University Comprehensive Cancer Center
Collaborators
National Institute on Aging (NIA)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This clinical trial compares audio brochures and video brochures to usual care for increasing colorectal cancer (CRC) screening among adults living in Appalachia. Adults living in rural Appalachia experience increased rates of CRC, possibly due to the unique barriers to screening this population faces, such as lower socioeconomic status, limited health literacy, and less access to healthcare. The fecal immunochemical test (FIT) is a common CRC screening technique which allows individuals to complete the test at home and mail the kit back. A limitation of the current process for FIT screening outreach is that the instruction materials are heavy in text and not appropriate for individuals with limited health literacy. The audio and video brochures used in this clinical trial are instruction materials that have been specially designed to be appropriate for individuals of all health literacy levels. Providing these tailored audio and video brochures with the FIT kits may increase CRC screening among adults living in Appalachia, compared to usual care.
Detailed Description
PRIMARY OBJECTIVE: I. Conduct a pilot study of the two developed mail-based FIT outreach interventions versus (vs.) mailed usual care materials to establish acceptability and obtain preliminary efficacy data on increasing CRC screening. OUTLINE: Participants are randomized to 1 of 3 arms. ARM I: Participants receive the FIT kit and usual care on study. ARM II: Participants receive the FIT kit with an audio brochure, disposable gloves and stool collection device, and scheduled reminder on study. ARM III: Participants receive the FIT kit with a video brochure, disposable gloves and stool collection device, and scheduled reminder on study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Carcinoma

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
94 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm I (FIT, usual care)
Arm Type
Active Comparator
Arm Description
Participants receive the FIT kit and usual care on study.
Arm Title
Arm II (FIT, audio brochure, reminder)
Arm Type
Experimental
Arm Description
Participants receive the FIT kit with an audio brochure, disposable gloves and stool collection device, and scheduled reminder on study.
Arm Title
Arm III (FIT, video brochure, reminder)
Arm Type
Experimental
Arm Description
Participants receive the FIT kit with a video brochure, disposable gloves and stool collection device, and scheduled reminder on study.
Intervention Type
Other
Intervention Name(s)
Best Practice
Other Intervention Name(s)
standard of care, standard therapy
Intervention Description
Receive usual care
Intervention Type
Other
Intervention Name(s)
Fecal Immunochemical Test
Other Intervention Name(s)
FIT, iFOBT, immunoassay fecal occult blood test, immunochemical fecal occult blood test, Immunochemical FOBT, immunologic fecal occult blood test
Intervention Description
Receive FIT kit
Intervention Type
Behavioral
Intervention Name(s)
Health Education
Intervention Description
Receive audio brochure
Intervention Type
Behavioral
Intervention Name(s)
Health Education
Intervention Description
Receive video brochure
Intervention Type
Other
Intervention Name(s)
Scheduled Notification
Other Intervention Name(s)
ScheduledNotification
Intervention Description
Receive scheduled reminder
Intervention Type
Other
Intervention Name(s)
Survey Administration
Intervention Description
Ancillary studies
Primary Outcome Measure Information:
Title
Fecal immunochemical test (FIT) return
Description
Will estimate FIT return using proportions for each study group. Both comparisons (each intervention compared to control) will be a two-sample test of proportions (intent-to-treat analysis) using a one-sided alpha of 0.1 due to the preliminary nature of the study. Will estimate critical parameters with point estimates and 95% confidence intervals and provide a preliminary test of effectiveness on FIT completion.
Time Frame
At 2 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
64 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Mid-life men and women (50-64 years old) Live in Appalachia Had a medical visit in the past two years Are at average-risk for CRC (no history of CRC, polyps, inflammatory bowel disease, family history of CRC or hereditary CRC syndromes) Are not within CRC screening guidelines (no fecal occult blood test/FIT in the past year; flexible sigmoidoscopy in past five years; colonoscopy in past ten years)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mira Katz, PhD, MPH
Organizational Affiliation
Ohio State University Comprehensive Cancer Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ohio State University Comprehensive Cancer Center
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Audio and Video Brochures for Increasing Colorectal Cancer Screening Among Adults Living in Appalachia

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