Medical Student Firearm Safety Counseling Follow-Up Study

NCT ID: NCT06241937

Last Updated: 2025-07-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

176 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-08-15

Study Completion Date

2025-06-01

Brief Summary

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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.

Detailed Description

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Conditions

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Medical Student Knowledge of Firearm Violence Epidemiology Medical Student Knowledge About Firearm Safety Procedures Medical Student-initiated Clinical Firearm Safety Counseling

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Survey responses and student performances during the simulated patient encounter for members of the DGSOM Class of 2027 who consent to study participation will be compared with those of the students in the DGSOM Classes of 2023 and 2024 in the investigators' previous study of firearm safety counseling training, who consented to the future use of their study data (ClinicalTrials.Gov ID: NCT05242627). Surveys and simulated patient encounter scenario will be identical in both studies, to allow for optimal comparison to the historical controls.
Primary Study Purpose

OTHER

Blinding Strategy

NONE

The simulated patient encounter used for this study is a regular component of the DGSOM curriculum used to assess student skills in history taking and physical examination. Students will not be told specifically before the activity that one of the assessments will be whether or not they counseled the simulated patient about firearm safety. Following the activity, the students will be invited to provide informed consent for investigators to view video recordings of the activity for educational research. The firearm screening and counseling performance will not be a factor in a student's grade for the simulated patient encounter.

Study Groups

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DGSOM Class of 2027

Group Type EXPERIMENTAL

Expanded Clinical Firearm Safety Counseling Training

Intervention Type BEHAVIORAL

Members of the DGSOM class of 2027 will participate in a mandatory 3.5 hour training session as a part of the regular curriculum that will include: (1) didactic information on firearm violence epidemiology; (2) suicide epidemiology and introduction to lethal means restriction; (3) firearm safety counseling techniques; (4) a panel of firearm violence survivors / trauma interventionists; and (5) a small group session with discussions of the aforementioned topics and a demonstration of a patient encounter using a standardized patient actor depicting a clinical scenario warranting firearm safety counseling. The training will be taught by faculty members, invited subject matter experts, senior medical students, and the DGSOM Standardized Patient Program.

Interventions

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Expanded Clinical Firearm Safety Counseling Training

Members of the DGSOM class of 2027 will participate in a mandatory 3.5 hour training session as a part of the regular curriculum that will include: (1) didactic information on firearm violence epidemiology; (2) suicide epidemiology and introduction to lethal means restriction; (3) firearm safety counseling techniques; (4) a panel of firearm violence survivors / trauma interventionists; and (5) a small group session with discussions of the aforementioned topics and a demonstration of a patient encounter using a standardized patient actor depicting a clinical scenario warranting firearm safety counseling. The training will be taught by faculty members, invited subject matter experts, senior medical students, and the DGSOM Standardized Patient Program.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

Eligibility Criteria is limited to being a member of the DGSOM Class of 2027.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of California, Davis

OTHER

Sponsor Role collaborator

University of California, Los Angeles

OTHER

Sponsor Role lead

Responsible Party

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Gary Holland, MD

Distinguished Professor of Ophthalmology

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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David Geffen School of Medicine at UCLA

Los Angeles, California, United States

Site Status

Countries

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United States

Other Identifiers

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20-000968A

Identifier Type: -

Identifier Source: org_study_id

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