MedPath

A Community Based Approach to Reducing Rural Cancer Disparities, Aim 2

Completed
Conditions
Cancer
Interventions
Other: CC&S
Registration Number
NCT02973022
Lead Sponsor
University of Wisconsin, Madison
Brief Summary

The aim of this study is to evaluate the impact of participation in Cancer Clear and Simple (CC\&S) educational sessions on cancer prevention and screening. The researchers will recruit 60 community members: 30 will receive CC\&S training (intervention group) and 30 will not (control group). All 60 will be surveyed about their intent to change their behavior at the beginning of the study and their actual behavior changes and their screening behavior 6 months after enrollment in the study.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
66
Inclusion Criteria
  • Wisconsin resident
Exclusion Criteria
  • None

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Community CC&S GroupCC&SOnce participants are randomized, they will be given survey 1. The intervention group in the community will be exposed to the modified CC\&S educational sessions in a series of 2 one hour and 15 minute sessions on consecutive Monday nights. A free meal will be provided at both educational sessions. Childcare will be provided for community sessions. Once the final educational session is completed, all participants will be given survey 2.
ACEC CC&S GroupCC&SOnce participants are randomized, they will be given survey 1. The intervention group at ACEC (Adams-Columbia Electric Company) will be exposed to the modified CC\&S educational sessions in a series of 6 thirty minute sessions before the work day begins over the course of several weeks. The researchers anticipate that two sessions will occur per week and therefore the delivery of the whole intervention will take 3 weeks. A free meal will be provided at all 6 educational sessions. Once the final educational session is completed, all participants will be given survey 2.
Primary Outcome Measures
NameTimeMethod
Change in behavioral intentUp to 3 weeks

All 60 participants (30 intervention, 30 control group) will be surveyed about their intent to change their behavior at the beginning of the study and their actual behavior changes and their cancer screening behavior 6 months after enrollment in the study.

Secondary Outcome Measures
NameTimeMethod
Change in cancer knowledgeUp to 6 months

Change in cancer knowledge measured before the educational session to after the session and duration of that knowledge as measured from right after the session to six months later.

Trial Locations

Locations (1)

University of Wisconsin Carbone Cancer Center

🇺🇸

Madison, Wisconsin, United States

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