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NCT02973022 Clinical Trial

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

Cancer Clinical Trial

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02973022
Other study ID # UW16048
Secondary ID 2016-0941A534253
Status Completed
Phase
First received
Last updated
Start date October 7, 2016
Est. completion date September 17, 2018

Study information
Verified date February 2019
Source University of Wisconsin, Madison
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.

Other known NCT identifiers
  • NCT02886325

Recruitment information / eligibility
Status Completed
Enrollment 66
Est. completion date September 17, 2018
Est. primary completion date September 17, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 25 Years and older
Eligibility Inclusion Criteria:

- Wisconsin resident

Exclusion Criteria:

- None

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• CC&S
Three educational modules -- Cancer Basics, Cancer Prevention, and Cancer Screening -- intended to increase cancer awareness. The full CC&S curriculum is currently available at http://chdi.wisc.edu/cancer-clear-simple-curriculum-rural-adaptation.

Locations
Country Name City State
United States University of Wisconsin Carbone Cancer Center Madison Wisconsin

Sponsors (3)
Lead Sponsor Collaborator
University of Wisconsin, Madison American Cancer Society, Inc., National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Change in behavioral intent 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. Up to 3 weeks
Secondary Change in cancer knowledge 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. Up to 6 months
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