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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03248661
Other study ID # 14-0662-P3H
Secondary ID
Status Completed
Phase Phase 3
First received
Last updated
Start date August 1, 2015
Est. completion date September 25, 2018

Study information

Verified date January 2019
Source University of Kentucky
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will randomly assign 220 men and women to either a social media intervention or a standard reminder system to have a repeat screening test for colo-rectal cancer.


Description:

Only persons initially screening by FIT (through a Rural Cancer Prevention Center service program) will be eligible for study participation. The objective is to test a social media-based intervention designed to promote annual repeat colo-rectal cancer screening using the Fecal Immunochemical Test (FIT) among person who have taken the FIT test once before. 220 men and women (50 to 75 years of age) will be recruited and randomly assigned to either the intervention condition (monthly social media contact) or a control condition (standard of care reminder for repeat testing one month before the annual test is due). The dependent variable will be whether volunteers requested and retuned a FIT kit with 60 days of the annual due date (one year from their initial screening).


Recruitment information / eligibility

Status Completed
Enrollment 220
Est. completion date September 25, 2018
Est. primary completion date September 25, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 30 Years to 75 Years
Eligibility Inclusion Criteria:

- must have completed and returned an initial FIT kit to us as part of a Rural Cancer Prevention Center service program to the community

Exclusion Criteria:

- visible blood in stool or prior diagnosis of cool-rectal cancer

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Now I'm Telling You
Messages will be sent trough Facebook, Twitter, Instagram, e-mail, texting or other electronic/social media specified by study volunteers.

Locations

Country Name City State
United States University of Kentucky Lexington Kentucky

Sponsors (2)

Lead Sponsor Collaborator
Richard Crosby Centers for Disease Control and Prevention

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Primary endpoint is a received completed FIT kit within 15 months after the participant received results from the original FIT test the endpoint is a received completed FIT kit 15 months
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