跳至主要内容
临床试验/NCT03207217
NCT03207217Unknown不适用

Virtual Training Role-Plays to Improve Patient Suicide Outcomes in Primary Care Settings

SIMmersion, LLC0 个研究点目标入组 91 人开始时间: 2017年7月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
91
主要终点
C-SSRS Lifeline/Recent Completion

研究概览

简要总结

SIMmersion, in collaboration with the Institute for Family Health (IFH) and the Educational Development Center (EDC) propose to develop a web-based training product, Suicide Prevention Role-plays for Interactive Training (SPiRIT), a series of 4 modules to train providers to more effectively manage patients who screen positive for risk of suicide in this Phase I/Phase II fast-track application. If funded, the team will develop the Risk Assessment module in Phase I and utilize a within group pre-post design to evaluate its feasibility. Twenty practicing clinicians will be recruited to utilize the module and complete a pre-post knowledge test. In Phase II, the team will develop Safety Planning, Access to Lethal Means, and Willingness to Accept a Referral modules. The efficacy of the product to positively influence patient outcomes will be tested with a Historically Controlled Trial (HCT) enlisting 65 practicing clinicians across five IFH sites. All providers will be trained and patient outcomes will be tracked for 6 months post training. This data set will be compared to 6 months of historical data for the same provider group. Primary outcomes of this study will measure the participants' ability in obtain improved patient outcomes related to: 1) rate of same-day C-SSRS Screening; 2) rate of suicide being added to the problem list; 3) rate of same-day safety planning; 4) rate of same day C-SSRS Lifeline/Recent Completion; 5) rate of same-day Risk Assessment; 6) rate of acceptance and attendance to within-Institute referrals for post intervention patients who are offered the referral at the first visit; 7) and lower rates of documented suicide attempts. Ultimately, the development and successful testing of this product would provide the US health care system a novel technology to scale up a clinician's confidence and skill to better manage patients who identify as at-risk for suicide. Additionally, if effective, this product will have a direct impact on patient outcomes, a vital component to any training product that attempts to train health care professionals. The utility and scalability of the proposed product will move health care systems toward the goal of zero deaths from suicide consistent with the Zero suicide approach.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Prevention
盲法
None

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

  • (1) Hold an active license issued by the State of New York for their profession and be in good standing; (2) actively see patients at an IFH site; and (3) have completed IFH's mandated suicide prevention training.

排除标准

  • (1) have not completed their IFH Suicide Prevention Training as outlined in the IFH's Suicide Prevention Training Policy; or (2) have uncorrected vision or hearing problems that prevent the person from using the software. Specific to Phase II an additional criteria is (3)participated in the Phase 1 feasibility testing.

结局指标

主要结局

C-SSRS Lifeline/Recent Completion

时间窗: Assessment will occur after a 6 month period of tracking patient records for each provider

Higher rates of same-day C-SSRS Lifeline/Recent Completion, if a positive screen;

Suicide addition to Problem List

时间窗: Assessment will occur after a 6 month period of tracking patient records for each provider

Higher rates of suicide being added to the problem list

C-SSRS Screening

时间窗: Assessment will occur after a 6 month period of tracking patient records for each provider

Higher rates of same-day C-SSRS Screening

Risk Assessment

时间窗: Assessment will occur after a 6 month period of tracking patient records for each provider

Higher rates of same-day Risk Assessment, if a positive screen

Within-Institute referrals

时间窗: Assessment will occur after a 6 month period of tracking patient records for each provider

Higher rates of acceptance and attendance to within-Institute referrals for post intervention patients who are offered the referral at the first visit

Documented suicide attempts

时间窗: Assessment will occur after a 6 month period of tracking patient records for each provider

Have lower rates of documented suicide attempts

Same-day Safety Planning, if a positive screen

时间窗: Assessment will occur after a 6 month period of tracking patient records for each provider

Higher rates of same-day Safety Planning, if a positive screen

次要结局

未报告次要终点

研究者

发起方
SIMmersion, LLC
申办方类型
Industry
责任方
Sponsor

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