Training Primary Care Physicians to Perform Melanoma Opportunistic Surveillance
Primary Purpose
Melanoma, Nevi, Skin Moles
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Educational training program
Sponsored by
About this trial
This is an interventional screening trial for Melanoma focused on measuring Training, Primary Health Care, Skin Cancer, Primary Care Physicians, Surveillance, Education
Eligibility Criteria
Inclusion Criteria for PCPs:
- is a practicing PCP in the section of General Internal Medicine of Northwestern Medicine
Exclusion Criteria for PCPs:
- is NOT a practicing PCP in the section of General Internal Medicine of Northwestern Medicine
Inclusion Criteria for Patients providing lesions to be photographed:
- is a patient of a PCP enrolled in the study
- is at least 18 years old
- able to read at a 6th grade level or higher
Exclusion Criteria for Patients providing lesions to be photographed:
- is NOT a patient of a PCP enrolled in the study
- under 18 years of age
- unable to read at a 6th grade level
Sites / Locations
- Northwestern Medicine: Division of General Internal Medicine and Geriatrics
- Northwestern University Feinberg School of Medicine Department of Dermatology
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
No Intervention
Arm Label
Educational training program
Control
Arm Description
PCPs randomized to the intervention group will receive the educational training program at the beginning of the study, extending over a maximum of five months.
PCPs randomized to the control group will have the option of receiving the educational training program at the end of the study.
Outcomes
Primary Outcome Measures
Change from baseline performance at 5 months (difference-in-difference)
The difference-in-difference (DID) approach will be used to test the hypothesis that the educational intervention improved knowledge, attitude concerning importance of skin exam, competence, confidence, and diagnostic performance. The difference-in-difference estimator compares outcomes between pre-tests and post-tests between PCPs who received the educational intervention and those who did not.
Each PCP will be the unit of observation. We will choose an appropriate functional form for each outcome.For each outcome, a DID estimator that is significant at p < 0.05 will support the hypothesis that the educational intervention improved outcomes. This analysis will be repeated for each of the five outcomes. We will use the Bonferroni correction for multiple comparisons.
Secondary Outcome Measures
Change in number of pigmented lesions referrals from three months prior and three months post randomization (Difference-in-Difference estimator)
The difference-in-difference (DID) approach will be used to test the hypothesis that the intervention reduced referrals of benign lesions. The model will be estimated using a random effects logistic regression to account for clustering due to repeated measures for each PCP (about 8 referrals before randomization and another 8 after the intervention). A 95% confidence interval for the odds ratio of α3 that falls below one will support the hypothesis.
Full Information
NCT ID
NCT02385253
First Posted
February 25, 2015
Last Updated
June 5, 2018
Sponsor
Northwestern University
1. Study Identification
Unique Protocol Identification Number
NCT02385253
Brief Title
Training Primary Care Physicians to Perform Melanoma Opportunistic Surveillance
Official Title
Training Primary Care Physicians to Perform Melanoma Opportunistic Surveillance
Study Type
Interventional
2. Study Status
Record Verification Date
September 2017
Overall Recruitment Status
Completed
Study Start Date
September 15, 2015 (Actual)
Primary Completion Date
July 23, 2017 (Actual)
Study Completion Date
July 23, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Northwestern University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This is a four-phase educational intervention for primary care practitioners (PCPs) to perform opportunistic melanoma surveillance. Based on prior research, the investigator will develop an interactive melanoma early detection skills training program for PCPs according to the principals of mastery learning. The proposed educational intervention will improve practicing PCPs' knowledge, competence, confidence, and diagnostic performance regarding pigmented lesions and attitude concerning importance of skin surveillance. In addition, this research aims to examine the clinical proficiency of PCPs regarding pigmented lesions. The proposed educational intervention will reduce the percentage of benign lesions referred to dermatology.
Detailed Description
Cutaneous melanoma is considered a potentially curable disease if detected early. Primary care physicians (PCPs) are well positioned to detect early melanomas by performing opportunistic melanoma surveillance on the at-risk population during physical examination. Opportunistic surveillance means physician performance of visual inspection of skin exposed during your physical examination focused on the presenting condition. Opportunistic surveillance requires skills in both visual inspection of the skin and with magnification of the skin by a hand-held device, a dermoscope. (This research aims to 1) develop an easily disseminated, interactive melanoma early detection skills training program for PCPs and to 2) to examine the clinical proficiency of PCPs regarding pigmented lesions.
The knowledge to be gained by PCPs is essential to the development and successful introduction of a method for physicians to learn how to perform opportunistic surveillance for melanoma. By evaluating means of encouraging and facilitating opportunistic surveillance for melanoma, an educational program may eventually be brought into widespread use in training PCPs.
In addition to a Pre-training Test and Post-training Test, each of the phases of the educational training program is described below:
Knowledge Acquisition The Knowledge Acquisition phase will be delivered via personal computer/tablet. It will take about one hour to complete. The one-hour course consists of case histories and videos in which the following are presented: 1) threshold rules of visual inspection, 2) benefit of magnification with dermoscopy to assist with diagnosis, and 3) demonstration of the 3-point checklist of dermoscopy.
Skills Assessment The Skills Assessment phase will be delivered via smartphone. The program may be intermittently accessed taking up to two weeks to complete. The PCP will be asked to review and make simulated management decisions on 20 case vignettes with clinical images of body surfaces and dermoscopy of individual lesions. Clinical practice will be simulated with the requirement that you make a decision to refer to dermatology or a decision that a referral is not needed. If a biopsy is performed in the case vignette, the pathology report will be provided, and the PCP will be asked the next step in the patient's care. Performance feedback will be provided.
Deliberate Practice The Deliberate Practice phase will be delivered via smartphone. It will take between 1-8 weeks to complete. The PCP will be asked to review additional cases with visual inspection and dermoscopy to improve aspects of your performance that have demonstrated weakness. Individual strengths and weaknesses will be assessed, and personalized feedback will be provided. After achieving competency with the simulated cases, the research staff will provide the PCP with a DermScope device (a smartphone fitted with a dermoscope) to use in the next phase.
Clinical Proficiency The Clinical Proficiency phase will take place in the clinical practice of the PCP over the course of 1-8 weeks. The PCP will be asked to use the DermScope to capture and transmit at least 12 lesions. Informed consent will be obtained from each patient prior to obtaining the non-identifying images. During image capture, each photograph is marked by the DermScope program with the date, time, and the clinical assessment form (CAF). The image will be transmitted to the teleconsultant (PI), who will assign a unique identification number to the image and the data. The PI will render an opinion within 72 hours regarding the need to refer the patient to dermatology or reassure the patient. The PCP will be asked to make a decision regarding the management of the patient and communicate this decision as needed to the patient.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Melanoma, Nevi, Skin Moles
Keywords
Training, Primary Health Care, Skin Cancer, Primary Care Physicians, Surveillance, Education
7. Study Design
Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
89 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Educational training program
Arm Type
Active Comparator
Arm Description
PCPs randomized to the intervention group will receive the educational training program at the beginning of the study, extending over a maximum of five months.
Arm Title
Control
Arm Type
No Intervention
Arm Description
PCPs randomized to the control group will have the option of receiving the educational training program at the end of the study.
Intervention Type
Behavioral
Intervention Name(s)
Educational training program
Intervention Description
The educational training program (intervention) consists of four sequential phases:
Knowledge Acquisition
Skills Assessment
Deliberate Practice
Clinical Proficiency
Primary Outcome Measure Information:
Title
Change from baseline performance at 5 months (difference-in-difference)
Description
The difference-in-difference (DID) approach will be used to test the hypothesis that the educational intervention improved knowledge, attitude concerning importance of skin exam, competence, confidence, and diagnostic performance. The difference-in-difference estimator compares outcomes between pre-tests and post-tests between PCPs who received the educational intervention and those who did not.
Each PCP will be the unit of observation. We will choose an appropriate functional form for each outcome.For each outcome, a DID estimator that is significant at p < 0.05 will support the hypothesis that the educational intervention improved outcomes. This analysis will be repeated for each of the five outcomes. We will use the Bonferroni correction for multiple comparisons.
Time Frame
Baseline and 5 months
Secondary Outcome Measure Information:
Title
Change in number of pigmented lesions referrals from three months prior and three months post randomization (Difference-in-Difference estimator)
Description
The difference-in-difference (DID) approach will be used to test the hypothesis that the intervention reduced referrals of benign lesions. The model will be estimated using a random effects logistic regression to account for clustering due to repeated measures for each PCP (about 8 referrals before randomization and another 8 after the intervention). A 95% confidence interval for the odds ratio of α3 that falls below one will support the hypothesis.
Time Frame
Three months prior randomization, Three months post intervention
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria for PCPs:
is a practicing PCP in the section of General Internal Medicine of Northwestern Medicine
Exclusion Criteria for PCPs:
is NOT a practicing PCP in the section of General Internal Medicine of Northwestern Medicine
Inclusion Criteria for Patients providing lesions to be photographed:
is a patient of a PCP enrolled in the study
is at least 18 years old
able to read at a 6th grade level or higher
Exclusion Criteria for Patients providing lesions to be photographed:
is NOT a patient of a PCP enrolled in the study
under 18 years of age
unable to read at a 6th grade level
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
June K Robinson, MD
Organizational Affiliation
Northwestern University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northwestern Medicine: Division of General Internal Medicine and Geriatrics
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Facility Name
Northwestern University Feinberg School of Medicine Department of Dermatology
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
29404948
Citation
Robinson JK, Jain N, Marghoob AA, McGaghie W, MacLean M, Gerami P, Hultgren B, Turrisi R, Mallett K, Martin GJ. A Randomized Trial on the Efficacy of Mastery Learning for Primary Care Provider Melanoma Opportunistic Screening Skills and Practice. J Gen Intern Med. 2018 Jun;33(6):855-862. doi: 10.1007/s11606-018-4311-3. Epub 2018 Feb 5.
Results Reference
background
PubMed Identifier
29637481
Citation
Robinson JK, MacLean M, Reavy R, Turrisi R, Mallett K, Martin GJ. Dermoscopy of Concerning Pigmented Lesions and Primary Care Providers' Referrals at Intervals After Randomized Trial of Mastery Learning. J Gen Intern Med. 2018 Jun;33(6):799-800. doi: 10.1007/s11606-018-4419-5. No abstract available.
Results Reference
background
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Training Primary Care Physicians to Perform Melanoma Opportunistic Surveillance
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