Web-based Education on Oral Cancer for Primary Care Physicians in Ohio

Creighton University

Status: Completed

Conditions: Oral Cancer

Treatments: Other: Web-based Educational Intervention

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT01424358

11-16008

7K23DE016890-07 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

Objective:

The experimental design is a one-site, randomized experimental web-based educational feasibility intervention trial, with approximately 50% primary care physicians (PCPs) in the intervention group and approximately 50% PCPs on the control group, giving a total of 159 participants. All 159 participants have willingly provided their e-mail addresses, as part of a survey they previously completed entitled, "Survey of Health Professionals on Oral Cancer in Ohio- Intervention to Prevent Delayed Diagnosis of Oral Cancer."

Full description

The main specific aim is to determine the short-term effectiveness of a web-based educational intervention for primary care physicians (PCPs) in Ohio to improve the following:Index of knowledge of risk factors for oral cancer, and Index of knowledge of diagnostic procedures for oral cancer

The following hypothesis will be explored: The use of a web-based educational module for PCPs in Ohio regarding oral cancer will increase the proportion of the PCPs in the high score category for the following indices: Index of knowledge of risk factors of oral cancer, and Index of knowledge of diagnostic procedures for oral cancer

Enrollment: 10 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• The PCP's who participated in Specific Aim #2 (Survey of Healthcare Professionals on Oral Cancer in Ohio ) of the NIH K23 grant proposal, "Intervention to Prevent Delayed Diagnosis of Oral Cancer", will be eligible to participate in this Web-Based Education on Oral Cancer.
• Possessing the ability to give voluntary consent to participate. Participating in the web-based educational intervention is am implication of consent.
• All participants are expected to be relatively healthy.

Exclusion criteria

• Unable to have access to the internet to be able to participate in the web-based education.

Trial design

10 participants in 1 patient group

Web-based Educational

Experimental group

Treatment:

Other: Web-based Educational Intervention