- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05761782
Engaging Diverse and Underserved Communities in Cancer Awareness Training and Education (EDUCATE)
Engaging Diverse and Underserved Communities in Cancer Awareness Training and Education (EDUCATE)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Objective: To determine the effects of health education, outreach, and training activities on cancer control and prevention knowledge, attitudes, beliefs, and behaviors among the University of California Davis, Comprehensive Cancer Center's (UCDCCC) catchment area residents. There are 3 Specific Aims for EDUCATE.
Specific Aim 1: To educate catchment area residents on modifiable risk factors for cancer (e.g., screening, behavior, vaccination) and the importance of participation in cancer research.
Specific Aim 2: Provide participants with educational materials on cancer prevention, screening, and vaccination.
Specific Aim 3: Evaluate the effectiveness of the health education, outreach, and training through the analyses of quantitative and qualitative data collected from the health education activities.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Alex Gori, B.S.
- Phone Number: 916-703-5165
- Email: acgori@ucdavis.edu
Study Contact Backup
- Name: Neha Singh, B.S.
- Phone Number: 916-734-5434
- Email: nehsingh@ucdavis.edu
Study Locations
-
-
California
-
Sacramento, California, United States, 95817
- Recruiting
- University of California, Davis Comprehensive Cancer Center
-
Contact:
- Alex Gori, B.S.
- Phone Number: 916-703-5165
- Email: acgori@ucdavis.edu
-
Contact:
- Neha Singh, B.S.
- Phone Number: 916-734-5434
- Email: nehsingh@ucdavis.edu
-
Principal Investigator:
- Julie Dang, Ph.D.
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- UCDCCC (University of California, Davis Comprehensive Cancer Center) Catchment Area Population
Exclusion Criteria:
- Above age 80
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
University of California, Davis Comprehensive Cancer Center's Catchment Area Population
Behavioral Intervention: Education and Training on Cancer Prevention and Education
|
To educate catchment area residents on modifiable risk factors for cancer (e.g., screening, behavior, vaccination) and the importance of participation in cancer research.
Provide participants with educational materials on cancer prevention, screening, and vaccination.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
EDUCATE Pre-Presentation Participant Survey
Time Frame: 2 years
|
Assessment of participant's experience with cancer screening (Breast, Colorectal, Cervical, Lung or Prostate)
|
2 years
|
|
EDUCATE Post-Presentation Participant Survey and Evaluation
Time Frame: 2 years
|
Assessment of participant's likelihood to get a cancer screening (Breast, Colorectal, Cervical, Lung or Prostate)
|
2 years
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Julie Dang, Ph.D., University of California, Davis
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 1992110-1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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