ClinicalTrials.Veeva

Menu

Evaluation of an Education Program to Increase Knowledge and Participation in Clinical Trials Among Racial/Ethnic and Rural Populations

The Ohio State University logo

The Ohio State University

Status

Completed

Conditions

Malignant Solid Neoplasm
Hematopoietic and Lymphoid System Neoplasm

Treatments

Other: Educational Intervention
Other: Survey Administration
Behavioral: Health Education

Study type

Interventional

Funder types

Other

Identifiers

NCT06112002
OSU-21293
NCI-2022-04986 (Registry Identifier)

Details and patient eligibility

About

This clinical trial evaluates a culturally tailored educational outreach intervention for increasing clinical trial knowledge, referral, and participation among racial/ethnic minority and rural populations. Clinical trials are research studies that involve people. Through clinical trials, researchers are able to determine whether new treatments are safe and effective and work better than current treatments. Clinical trials can also help find new ways to prevent and detect cancer and improve the quality of life for people during and after treatment. Recruitment and retention of underrepresented groups in clinical trials remains a challenge. Racial and ethnic minority groups bear a disproportionate burden of cancer compared with other groups yet these populations continue to be underrepresented in clinical trials. This clinical trial uses community health educators (CHEs) to facilitate individual and group education sessions to improve knowledge of what constitutes a clinical trial, the value of participating in clinical trials, and why it is important for racial/ethnic minorities to participate in clinical trials.

Full description

PRIMARY OBJECTIVE:

I. To implement culturally tailored educational outreach activities with the goal of increasing clinical trial (CT) knowledge, referral and participation among racial/ethnic and rural populations.

OUTLINE:

Participants attend an educational session with CHEs and receive educational materials on study.

Enrollment

78 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Adult males and females 18 years of age and older from Ohio
  • Will not let anyone who is not cognitively able to give voluntary informed consent take part in the education sessions

Trial design

Primary purpose

Health Services Research

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

78 participants in 1 patient group

Health Services Research (educational session and materials)
Experimental group
Description:
Participants attend an educational session with CHEs and receive educational materials on study.
Treatment:
Behavioral: Health Education
Other: Survey Administration
Other: Educational Intervention

Trial contacts and locations

1

Loading...

Central trial contact

The Ohio State University Comprehensive Cancer Center

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems