- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01905618
Tobacco Treatment Medical Education in 10 Medical Schools (MSQuit)
RCT for Smoking Cessation in 10 Medical Schools
Study Overview
Status
Conditions
Detailed Description
Ten medical schools are matched and then randomized, with 5 schools being randomized to MME and 5 schools to TE.
The primary aim of the study is to refine, implement, and evaluate whether a multi-modal educational (MME) approach is more effective than traditional educational (TE) approach for developing skill in the use of the 5As counseling steps for tobacco dependence treatment.
Multi-Modal Education(MME)Approach:
The MME approach includes: 1) a web-based course during the first-year of medical school; 2) a tobacco counseling role-play exercise; 3) training preceptors in the use of the 5As, preceptor observation of students in the use of 5As and providing instruction and feedback to students during a designated third-year clerkship rotation; and 4) a booster session provided during the third-year clerkship experience. These components are designed to enhance the interpersonal (e.g. 5As self-reported skill, tobacco treatment knowledge), intrapersonal (e.g. experiences observing 5As, experiences receiving 5As instruction), and organizational factors (e.g. clinic/system reminders) associated with optimal learning. This combination, primarily due to the web-based course/role play and preceptor facilitated teaching methods, is hypothesized to enhance medical students' 5As tobacco dependence treatment skills, compared to the TE approach.
Traditional Education (TE) Approach:
The TE approach represents "usual care" and includes the current content and method for tobacco teaching among medical schools. TE content typically includes knowledge in the basic science of tobacco use (e.g. health consequences of tobacco use and passive smoking), and the knowledge and practice of tobacco dependence treatment. All schools prior to randomization met the inclusion criteria that the curriculum devoted no more than four hours to tobacco.
The RCT's secondary aims address the potential impact of the interpersonal, intrapersonal, and organizational factors on tobacco dependence treatment counseling skills. The hypothesis is that these factors mediate the relationship between the MME curriculum approach and the primary outcome, observed 5As counseling skill, and that the MME approach will outperform the TE approach in each of these areas. This study also will assess the feasibility of implementing the MME across medical schools.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Alabama
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Birmingham, Alabama, United States, 35294
- University of Alabama-Birmingham
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California
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Stanford, California, United States, 94305
- Stanford University School of Medicine
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District of Columbia
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Washington, District of Columbia, United States, 20007
- Georgetown University School of Medicine
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Iowa
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Iowa City, Iowa, United States, 52242
- University of Iowa Carver College of Medicine
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Kentucky
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Lexington, Kentucky, United States, 40536
- University of Kentucky College of Medicine
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Louiville, Kentucky, United States, 40202
- University of Louisville School of Medicine
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Louisiana
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Shreveport, Louisiana, United States, 71130
- Louisiana State University Health Sciences Center-Shreveport
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Massachusetts
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Boston, Massachusetts, United States, 02115
- Harvard School of Public Health
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Worcester, Massachusetts, United States, 01655
- University of Massachusetts Medical School
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Minnesota
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Minneapolis, Minnesota, United States, 55414
- University of Minnesota Medical School
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Nebraska
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Omaha, Nebraska, United States, 68178
- Creighton University School of Medicine
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Ohio
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Columbus, Ohio, United States, 43210
- The Ohio State University
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Pennsylvania
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Philadelphia, Pennsylvania, United States, 19104
- University of Pennsylvania Perelman School of Medicine
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
Medical schools must have:-at least 90 first year medical students
- third year OSCEs, willing to add a tobacco-related OSCE, and able to provide access to each student's OSCE
- a tobacco curriculum not exceeding a total of four hours over the four years
- the flexibility within their curriculum to add and adopt new tobacco cessation modules
- willing and able to require first year students to enroll in the web-based course and to award credit for its successful completion
- a curriculum that includes a third year Family Medicine or Internal Medicine Clerkship
- resources to allow web-based training and electronic contact with students
- the ability to allow first and third year medical students to be surveyed
Exclusion Criteria:
Medical schools are excluded if they do not have:
- at least 90 first year medical students
- a third year OSCE, and are not willing to add a tobacco-related OSCE or able to provide access to student OSCEs
- a tobacco curriculum of less than four hours over the four years
- the flexibility within their curriculum to add and adopt new tobacco cessation modules
- the capacity to require first year students to enroll in the web-based course and to award credit for successful completion of the course
- a curriculum that includes a third year Family Medicine or Internal Medicine Clerkship
- resources to allow web-based training and electronic contact with students
- the ability to allow first and third year medical students to be surveyed
Study Plan
How is the study designed?
Design Details
- Primary Purpose: PREVENTION
- Allocation: RANDOMIZED
- Interventional Model: FACTORIAL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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EXPERIMENTAL: Multi Modal Education (MME)
Medical students in the medical schools randomized to the MME will receive four interventions during the course of their medical education.
The four interventions/components are: 1) web-based curriculum on tobacco dependence treatment; 2)tobacco counseling role play; 3) preceptor training and teaching medical students, preceptor modeling the 5As, student observation, and student feedback; and 4)booster session.
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The University of Massachusetts Medical School's web-based course, "Basic Skills for Working with Smokers" was adapted for this Randomized Controlled Trial (RCT).
The goal is to provide standardized information in the following core tobacco content areas: epidemiology of tobacco use, health consequences of tobacco use, nicotine dependence and withdrawal assessment, and provision of behavioral and pharmacotherapy tobacco treatment.
The course is 3 hours in length and can be completed at the student's convenience.
The dean and the course director at each medical school required that the first year medical students complete the web-based curriculum prior to the next component of the study, the role play.
Other Names:
The goal of the role play is to provide each student with the opportunity to apply what he/she learned in the web-based curriculum (the 5 As and the physician delivered intervention approach).
The one hour session begins with a video of a patient-centered counseling approach which incorporates the 5A intervention presented in the web-based course.
This is followed by a 30 minute role play session including various scenarios with physician/patient interaction.
Students role play either as physician, patient or observer for each scenario.
Other Names:
The goal of this intervention is to train preceptors in the use of the 5As with their patients and to teach and motivate their medical students to use the 5As.
The academic detailing approach is used to provide a standardized 30 to 45 minute group training session during the third year clerkship.
All preceptors and medical students are encouraged to intervene with patients who smoke.
Preceptors are encouraged to model the 5As, observe and give feedback to the medical student in its use.
Study-tailored handouts are available for preceptors and students.
This component is implemented with the study cohort in their third year of medical school.
Other Names:
The last component of the intervention, a small group booster session, occurs during the third year of medical school.
A five minute video reviews the use of the 5As and patient-centered counseling strategies.
Faculty facilitate a small group discussion after viewing the video.
Other Names:
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NO_INTERVENTION: Traditional Education (TE)
Medical schools randomized to the Traditional Education (TE) will represent usual care and includes the current content and mode for tobacco teaching in the medical school.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Objective Structured Clinical Exam (OSCE)
Time Frame: Up to 2 years
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The primary outcome is the observed tobacco treatment 5As counseling skills as measured by the Objective Structured Clinical Examination (OSCE), the standard method for evaluating medical student skill level at all U.S. medical schools.
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Up to 2 years
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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A self-report survey instrument for tobacco treatment counseling skill level
Time Frame: Up to 3 years
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The secondary outcome is the self report survey completed by first year medical students and then the followup assessment when completing the third year of medical school.
All followup assessments will be completed by October 2013.
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Up to 3 years
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Collaborators and Investigators
Collaborators
Publications and helpful links
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
- Mental Disorders
- Chemically-Induced Disorders
- Substance-Related Disorders
- Tobacco Use Disorder
- Physiological Effects of Drugs
- Neurotransmitter Agents
- Molecular Mechanisms of Pharmacological Action
- Autonomic Agents
- Peripheral Nervous System Agents
- Cholinergic Agents
- Ganglionic Stimulants
- Nicotinic Agonists
- Cholinergic Agonists
- Nicotine
Other Study ID Numbers
- 13353
- 5R01CA136888 (NIH)
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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