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临床试验/NCT06241937
NCT06241937已完成不适用

A Prospective, Longitudinal Study of a Revised Firearm Safety Curriculum for Pre-Clinical Medical Students

University of California, Los Angeles2 个研究点 分布在 1 个国家目标入组 176 人开始时间: 2023年8月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
176
试验地点
2
主要终点
Medical Student Knowledge about Firearm violence and Attitudes about Physician Counseling.

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

盲法说明

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.

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Medical Student Knowledge about Firearm violence and Attitudes about Physician Counseling.

时间窗: 6 months

Data will be collected from student surveys conducted prior to training, immediately after training, and 6 months after training, the latter administered immediately following the simulated patient encounter. Students will be invited to provide informed consent for use of survey data for educational research.

Prevalence of medical student screening for access to firearms and counselling about firearm safety.

时间窗: 1 Day

The proportion of first-year medical students in the Class of 2027 who assess for access to firearms and counsel about firearm safety in a simulated patient encounter will be based on reporting by the simulated patient actor after the activity, for students who consent to use of data from the activity for educational research.

Firearm Safety Counseling

时间窗: 1 Day

For students who consent to use of data recorded from videos of their simulated patient encounter, investigators will score the quality of the counseling, if performed, based on prospectively defined criteria.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Gary Holland, MD

Distinguished Professor of Ophthalmology

University of California, Los Angeles

研究点 (2)

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