Firearm Safety Counseling for Gun Violence Prevention
Trial Summary
What is the purpose of this trial?
The preclinical curriculum related to firearm violence and safety counseling at the UCLA David Geffen School of Medicine (DGSOM) has been expanded for the Class of 2027, informed by the results and conclusions of an initial study of firearm safety counseling by medical students (ClinicalTrials.gov ID: NCT05242627), which was conducted by the present study team. The 1-hour firearm safety counseling training session used in that study will be taught again to first-year medical students in the Class of 2027, but training will be augmented with additional instruction; the Class will receive additional comprehensive instruction on suicide risk assessment and will participate in small group breakout sessions, to facilitate the opportunity for students to discuss issues related to firearm violence as a public health issue and to practice firearm safety counseling with standardized patient actors (SPs). Assessment of access to firearms and firearm safety counseling will be added as a standard component of the Social History that students are taught to obtain from patients during clinical examinations. The goal of the expanded training is to increase the prevalence of medical student counseling when they are conducting a history and physical examination in a simulated patient encounter with an SP 6 months after the initial training session, when compared to results from the initial study. The scenario provided to the SP will be identical to that used in the initial study and is a situation in which firearm safety counseling is warranted. Students will participate in a survey to ascertain their knowledge of firearm violence and their attitudes about physician counseling about firearm safety, prior to formal instruction. Informed consent will be obtained from students to use their responses in educational research. Following the didactic and small group sessions, students will be asked to complete a post-training survey that is similar to the original survey, as a means of assessing knowledge gained and any change in attitudes about physician counseling. The simulated patient encounter will occur approximately 6 months later, after which students will complete another survey to determine retention of knowledge and their experience during the simulated patient encounter. Students will not be told before the encounter that they will be evaluated regarding firearm safety counseling. The SP will identify which students did and did not raise the issue of firearm safety. Videos recorded of each students' sessions (routinely obtained for grading purposes) will be viewed by investigators for those students who provide informed consent, to determine the quality of counseling, if it was conducted. Results from this follow-up study will be compared to the results of the initial study as a historical control, to determine whether augmentation of firearm safety counseling training above a 1-hour didactic session increases firearm safety counseling by medical students in a clinical setting and whether it improves retention of knowledge about firearm violence.
Will I have to stop taking my current medications?
The trial does not specify whether participants need to stop taking their current medications.
What data supports the effectiveness of the treatment Expanded Clinical Firearm Safety Counseling Training?
Is Firearm Safety Counseling safe for participants in clinical trials?
How is the Expanded Clinical Firearm Safety Counseling Training different from other treatments for gun violence prevention?
This treatment is unique because it focuses on training healthcare providers, particularly in family practice and pediatrics, to effectively counsel patients on firearm safety, which is not commonly included in medical education. It uses resources like video training and curriculum guides to improve providers' confidence and knowledge in discussing safe firearm practices with patients.348910
Eligibility Criteria
This trial is for members of the UCLA David Geffen School of Medicine (DGSOM) Class of 2027. It aims to assess and enhance their skills in firearm safety counseling.Inclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Training
Students receive a 1-hour firearm safety counseling training session, augmented with additional instruction on suicide risk assessment and small group breakout sessions.
Simulated Patient Encounter
Approximately 6 months after the initial training, students participate in a simulated patient encounter to assess retention of knowledge and application of firearm safety counseling.
Follow-up
Participants are monitored for retention of knowledge and effectiveness of training through surveys conducted prior to training, immediately after training, and 6 months after training.
Treatment Details
Interventions
- Expanded Clinical Firearm Safety Counseling Training
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Who Is Running the Clinical Trial?
University of California, Los Angeles
Lead Sponsor
University of California, Davis
Collaborator