Ignite Creation Date:
2024-05-06 @ 11:15 AM
Last Modification Date:
2024-10-26 @ 12:42 PM
Study NCT ID:
NCT03473587
Status:
UNKNOWN
Last Update Posted:
2018-03-22
First Post:
2018-01-18
Brief Title:
Promoting Colorectal Cancer Screening in Rural Emergency Departments
Sponsor:
University of Kentucky
Organization:
University of Kentucky
Study Overview
Official Title:
Promoting Colorectal Cancer Screening in Rural Emergency Departments
Status:
UNKNOWN
Status Verified Date:
2018-03
Last Known Status:
RECRUITING
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
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
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None