Colon Cancer Prevention Study
Primary Purpose
Colorectal Cancer
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Behavioral Messages
Generic Messages
Sponsored by
About this trial
This is an interventional prevention trial for Colorectal Cancer focused on measuring Colon, Cancer, Screening, Prevention, Information
Eligibility Criteria
Inclusion Criteria:
- Female
- Ages 50-80 years old
Sites / Locations
- University of North Carolina at Chapel Hill
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
1
2
Arm Description
Behavioral Message Arm
Generic Message Arm
Outcomes
Primary Outcome Measures
Elaboration using the Elaboration Likelihood Scale
Secondary Outcome Measures
Behavioral Intention to Engage in Colorectal Cancer Screening or Physical Activity
Full Information
NCT ID
NCT00924690
First Posted
April 6, 2009
Last Updated
July 6, 2010
Sponsor
University of North Carolina, Chapel Hill
1. Study Identification
Unique Protocol Identification Number
NCT00924690
Brief Title
Colon Cancer Prevention Study
Official Title
Disparities in Colorectal Cancer Prevention Behaviors
Study Type
Interventional
2. Study Status
Record Verification Date
July 2010
Overall Recruitment Status
Completed
Study Start Date
June 2009 (undefined)
Primary Completion Date
September 2009 (Actual)
Study Completion Date
October 2009 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
University of North Carolina, Chapel Hill
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The goal of this research study is to design messages which can help people learn more about how to prevent colon cancer. Eligible participants will be asked to review a series of short cancer prevention messages and share their opinions on them. Participants also need to fill out a short survey with questions on their background and attitudes and knowledge about physical activity and colon cancer. The whole study can be completed online and will take less than 1 hour. After completing the entire study, participants will receive $25.
If you are interested in participating in this study, please visit the following website:
https://surveys.chaicore.com/preventcancer/
Detailed Description
The goal of this research is to develop and test potential intervention messages which can be used to help increase colon cancer prevention behaviors. Two sets of intervention messages will be developed: generic and behavioral. Using a randomized control design the investigators will evaluate the behavioral messages among women. This message testing protocol will help them determine if the messages are relevant, acceptable, comprehensible, memorable, and motivating for the target audience. The investigators' hypothesis is that the behavioral messages will receive more positive ratings than the generic messages. If so, they will be used to promote cancer screening and physical activity in future intervention studies.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer
Keywords
Colon, Cancer, Screening, Prevention, Information
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
207 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
Behavioral Message Arm
Arm Title
2
Arm Type
Active Comparator
Arm Description
Generic Message Arm
Intervention Type
Other
Intervention Name(s)
Behavioral Messages
Intervention Description
Participants will read 10 behavioral messages about colon cancer screening and physical activity.
Intervention Type
Other
Intervention Name(s)
Generic Messages
Other Intervention Name(s)
Control
Intervention Description
Individuals will read 10 generic messages about colon cancer screening and physical activity.
Primary Outcome Measure Information:
Title
Elaboration using the Elaboration Likelihood Scale
Time Frame
This study is to be completed in one session. The outcome is measured immediately after reading messages
Secondary Outcome Measure Information:
Title
Behavioral Intention to Engage in Colorectal Cancer Screening or Physical Activity
Time Frame
This study is to be completed in one session. The outcome is measured immediately after reading messages
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Female
Ages 50-80 years old
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lucia A Leone, BA
Organizational Affiliation
UNC
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Marci K Campbell, PhD
Organizational Affiliation
UNC
Official's Role
Study Chair
Facility Information:
Facility Name
University of North Carolina at Chapel Hill
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27599
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Colon Cancer Prevention Study
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