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NCT05064423 Clinical Trial

Clinical Trials Outreach & Education

Knowledge, Attitudes, Practice Clinical Trial

Official title:
Clinical Trials Outreach & Education

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05064423
Other study ID # MCC-21235
Secondary ID 3P30CA076292-21S
Status Recruiting
Phase N/A
First received
Last updated
Start date June 15, 2021
Est. completion date September 1, 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 education and information about clinical trials and clinical trials participation. Investigators also aim to see if education makes a difference in increasing knowledge of clinical trials and clinical trials participation.

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date September 1, 2024
Est. primary completion date September 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - English or Spanish speaking - Able to provide informed consent - Reside in the Tampa Bay Area (Hillsborough, Pinellas, Polk or Pasco county)

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Clinical Trials Education Program
The Community Health Educator (CHE) will provide CT education and outreach to increase clinical trial knowledge and the importance of clinical trials research and participation. The clinical trials educational activities will include the use of NCI Colorectal Cancer resources and materials, including a PowerPoint presentation, clinical trials information, and online resources. The CHE will tailor the PowerPoint slides to ensure that they are culturally tailored, visually appealing, low-literacy, language appropriate and include appropriate visuals. The CTs educational sessions will be delivered in Spanish and English and will take approximately 45 minutes to 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 Participants Clinical Trials Knowledge To assess the impact of the educational intervention on participants knowledge and beliefs about clinical trials, participants will be asked to complete a survey prior to and after the educational intervention. The pre-assessment and post assessment survey includes 11 items assessing knowledge of clinical trials, risks and benefits to clinical trials participation, and the consent process. Additionally, the assessment includes 6 items to determine intentions to seek out information related to clinical trials, speak with one's healthcare provider about appropriate clinical trials, clinical trials participation, and talking with family/friends about participating in clinical trials. Change from baseline to immediately after receiving intervention
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