Clinical Trials Outreach & Education

NCT05064423 | Completed

• 2 other identifiers: MCC-212353P30CA076292-21S3
• Study Type: interventional
• Target: 85
• Locations: 1 country
• Sites: 1

Brief 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.

Conditions

Knowledge, Attitudes, Practice

Outcome Measures

Primary Outcomes (1)

• 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

Study Arms (1)

Clinical Trials Education

EXPERIMENTAL

Community Health Educators (CHE) will provide Clinical Trial Education to increase knowledge of Clinical Trials and the importance of Clinical Trial participation.

Behavioral: Clinical Trials Education Program

Interventions

Clinical Trials Education Program BEHAVIORAL

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.

Clinical Trials Education

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• English or Spanish speaking
• Able to provide informed consent
• Reside in the Tampa Bay Area (Hillsborough, Pinellas, Polk or Pasco county)

Sponsors & Collaborators

• National Cancer Institute (NCI): collaborator
• H. Lee Moffitt Cancer Center and Research Institute: lead

Study Sites (1)

Moffitt Cancer Center

Tampa, Florida, 33612, United States

Location

MeSH Terms

Conditions

Behavior

Study Officials

• Clement K Gwede, PhD, MPH, RN, FAAN

  Moffitt Cancer Center

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: HEALTH SERVICES RESEARCH
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 22, 2021
• First Posted: October 1, 2021
• Study Start: June 15, 2021
• Primary Completion: March 23, 2022
• Study Completion: March 23, 2022
• Last Updated: February 9, 2026

Record last verified: 2026-02

Locations

US (1)