- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01424358
Web-based Education on Oral Cancer for Primary Care Physicians in Ohio
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."
Study Overview
Status
Conditions
Intervention / Treatment
Detailed 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
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Nebraska
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Omaha, Nebraska, United States, 68178
- Creighton University School of Dentistry
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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.
Study Plan
How is the study designed?
Design Details
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Web-based Educational
|
The intervention group will be invited to participate in the web-based educational program.
PCPs in the intervention group will be asked to view the educational module which will be followed by an assessment.
This group will be tested on the following knowledge outcomes: Index of knowledge of risk factor for oral cancer and Index of knowledge of diagnostic procedures for oral cancer.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Index of knowledge of diagnostic procedure for oral cancer
Time Frame: An average of 8 months from the time of the initial email sent on 7/21/11.
|
The list of participants will be sent an initial email inviting them to view the module and complete a pre test (control group) or a post test (intervention group).
Reminder emails will be sent every 2 months for up to 6 months following the initial email.
It is expected that at least a 15% higher proportion of Intervention group PCPs will attain the high score category for each of this index, as compared to the Control group PCPs.
|
An average of 8 months from the time of the initial email sent on 7/21/11.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
To determine if a change in Stage of Diagnosis of Oral Cancer occurred for the particular year of Web-based Educational Intervention.
Time Frame: 3 years
|
Three years post-web-based education intervention data will be requested from Ohio Cancer Incidence Surveillance System (OCISS).
OCISS's cleaning and processing of the data takes approximately three years.
Comparison using Chi-square will be carried out pre- and post- intervention years.
|
3 years
|
Index of knowledge of risk factors for oral cancer.
Time Frame: An average of 8 months from the time of the initial email sent on 7/21/11.
|
The list of participants will be sent an initial email inviting them to view the module and complete a pre test (control group) or a post test (intervention group).
Reminder emails will be sent every 2 months for up to 6 months following the initial email.
It is expected that at least a 15% higher proportion of Intervention group PCP's will attain the high score category for this index, as compared to the Control group PCP's.
|
An average of 8 months from the time of the initial email sent on 7/21/11.
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Alvin G Wee, DDS, MS, MPH, Creighton University
Publications and helpful links
General Publications
- Jemal A, Thomas A, Murray T, Thun M. Cancer statistics, 2002. CA Cancer J Clin. 2002 Jan-Feb;52(1):23-47. doi: 10.3322/canjclin.52.1.23. Erratum In: CA Cancer J Clin 2002 Mar-Apr;52(2):119. CA Cancer J Clin 2002 May-Jun;52(3):181-2.
- Canto MT, Devesa SS. Oral cavity and pharynx cancer incidence rates in the United States, 1975-1998. Oral Oncol. 2002 Sep;38(6):610-7. doi: 10.1016/s1368-8375(01)00109-9.
- Silverman S Jr. Demographics and occurrence of oral and pharyngeal cancers. The outcomes, the trends, the challenge. J Am Dent Assoc. 2001 Nov;132 Suppl:7S-11S. doi: 10.14219/jada.archive.2001.0382.
- Mashberg A, Garfinkel L. Early diagnosis of oral cancer: the erythroplastic lesion in high risk sites. CA Cancer J Clin. 1978 Sep-Oct;28(5):297-303. doi: 10.3322/canjclin.28.5.297. No abstract available.
- Horowitz AM, Nourjah PA. Factors associated with having oral cancer examinations among US adults 40 years of age or older. J Public Health Dent. 1996 Fall;56(6):331-5. doi: 10.1111/j.1752-7325.1996.tb02460.x.
- Canto MT, Drury TF, Horowitz AM. Use of skin and oral cancer examinations in the United States, 1998. Prev Med. 2003 Sep;37(3):278-82. doi: 10.1016/s0091-7435(03)00124-5.
- Horowitz AM, Moon HS, Goodman HS, Yellowitz JA. Maryland adults' knowledge of oral cancer and having oral cancer examinations. J Public Health Dent. 1998 Fall;58(4):281-7. doi: 10.1111/j.1752-7325.1998.tb03010.x.
- Goodman HS, Yellowitz JA, Horowitz AM. Oral cancer prevention. The role of family practitioners. Arch Fam Med. 1995 Jul;4(7):628-36. doi: 10.1001/archfami.4.7.628. No abstract available.
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 11-16008
- 7K23DE016890-07 (U.S. NIH Grant/Contract)
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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