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Clinical Trial Summary

The overall goal is to develop a culturally appropriate and easy to disseminate educational intervention documented to improve cancer prevention and increase cancer screening behaviors in the rural Midwest.


Clinical Trial Description

Objective: To evaluate how a modified version of CC&S may reduce health disparities.

Specific Aim: To evaluate the impact of participation in CC&S educational sessions on cancer prevention and screening.

Study Design: To evaluate the impact of participation in CC&S educational sessions on cancer prevention and screening. The investigators 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 screening behavior 6 months after the beginning of the study.

Goal: The overall goal is to develop a culturally appropriate and easy to disseminate educational intervention documented to improve cancer prevention and increase cancer screening behaviors in the rural Midwest. ;


Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject)


Related Conditions & MeSH terms


NCT number NCT02886325
Study type Interventional
Source University of Wisconsin, Madison
Contact Rebecca J Schwei, MPH
Phone 608-262-4955
Email rschwei@medicine.wisc.edu
Status Not yet recruiting
Phase N/A
Start date September 2016
Completion date May 2017

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