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Clinical Trials/NCT03473587
NCT03473587
Unknown
N/A

Promoting Colorectal Cancer Screening in Rural Emergency Departments

University of Kentucky1 site in 1 country191 target enrollmentNovember 7, 2014

Overview

Phase
N/A
Intervention
Not specified
Conditions
Colorectal Cancer
Sponsor
University of Kentucky
Enrollment
191
Locations
1
Primary Endpoint
Change in colorectal cancer screening rate
Last Updated
8 years ago

Overview

Brief Summary

This trial will compare the effects of a culturally targeted intervention designed to assist participants to identify and overcome individual barriers to colorectal cancer (CRC) and to promote CRC screenings using motivational interviewing (Ml) delivered by a lay health advisor (LHA) compared to the current standard-of-care (distribution of a brochure describing CRC screening services offered by the hospital) on CRC screening compliance.

Detailed Description

The specific aim of this project is to adapt and pilot a tailored intervention to promote CRC screenings in a rural Appalachian Kentucky emergency department (ED) in order to: (a) evaluate the feasibility of providing a cancer screening promotion intervention in an emergency department (ED) that serves a rural Appalachian community; and (b) assess the effects of the intervention on barriers to CRC screening, stage of readiness to screen and CRC screening engagement. The first phase of the project will involve the adaptation and pretesting of the intervention. This phase will take approximately 6 months. The second phase of the project will involve piloting the intervention and evaluating its efficacy and feasibility and will take place over the following 18 months. We will conduct a randomized controlled trial to examine the efficacy and feasibility of delivering the LHA delivered MI intervention to promote CRC screening in persons waiting in a rural Appalachian emergency department (ED) for non urgent complaints. We will evaluate efficacy by measurement of CRC screening status at baseline and three and six months post intervention.

Registry
clinicaltrials.gov
Start Date
November 7, 2014
End Date
May 30, 2018
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jennifer Hatcher

Principal Investigator

University of Kentucky

Eligibility Criteria

Inclusion Criteria

  • 50+ years of age
  • Rural Appalachian resident
  • No personal history of colorectal cancer
  • No cognitive impairment
  • Ability to speak and understand English
  • Has not had one of the following colorectal cancer screening tests--
  • Fecal Occult Blood Test within the past year
  • Flexible sigmoidoscopy within the past five years, or
  • Colonoscopy within the past ten years

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Change in colorectal cancer screening rate

Time Frame: 6 months

Number of participants that seek out colorectal cancer screening after a motivational interview with a lay health advisor compared to standard of care (being provided a screening brochure)

Study Sites (1)

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