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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05064410
Other study ID # MCC-19103
Secondary ID 3P30CA076292-21S
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date May 11, 2017
Est. completion date April 2024

Study information

Verified date March 2024
Source H. Lee Moffitt Cancer Center and Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to provide educational materials and information regarding colorectal cancer (CRC), CRC screenings, and United States Preventive Services Task Force's (USPSTF) screening recommendations. USPSTF recommends screening for colorectal cancer starting at age 45 years and continuing until age 75 years.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 188
Est. completion date April 2024
Est. primary completion date April 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 45 Years to 75 Years
Eligibility Inclusion Criteria: - Between 45 and 75 years of age - Spanish or English speaking - Able to provide informed consent - Reside in the Tampa Bay area (namely Hillsborough, Pinellas, Polk or Pasco county) Exclusion Criteria: - Does not meet inclusion criteria

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Educational Intervention
The colorectal cancer (CRC) educational activities will include the use of NCI CRC resources and materials, including a PowerPoint presentation, and CRC educational models and displays. The CRC education will be delivered in Spanish and English, and will consist of pre and post knowledge assessments including screening and behavioral intention questions. The educational intervention will take approximately 45 minutes-1 hour.

Locations

Country Name City State
United States Moffitt Cancer Center Tampa Florida

Sponsors (2)

Lead Sponsor Collaborator
H. Lee Moffitt Cancer Center and Research Institute National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Knowledge Related to Colorectal Cancer Risk, Prevention, and Screening Pre and post assessment surveys completed by participants will consist of 14 questions assessing knowledge of CRC, risk factors, and screening options and recommendations. Assessments also include 5 questions to determine intentions to change screening/health behaviors, speaking to one's healthcare provider about screening, getting screened, and talking with family/friends about CRC and CRC screening.
3-month follow up survey consists of 5 sections to determine CRC knowledge, screening behavior since baseline, future screening plans, talking with family and friends about CRC screening, and behavior changes in eating habits and physical activity since partaking in the educational session.
6-month survey consists of 5 questions about screening since the 3-month follow up survey. Those needing to complete the 6-month follow up survey are those that were screened at the time of the 3-month follow-up but had not received final diagnostic results.
Baseline, immediately following intervention, at 3 months and at 6 months
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