Maximizing Extubation Outcomes Through Educational and Organizational Research: Think NIV Pilot Study
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 1,328
- 试验地点
- 2
- 主要终点
- Number of ICU Team Members (Learners) Who Received Education
研究概览
简要总结
This study will pilot test three strategies designed to speed implementation of preventive post-extubation noninvasive ventilation (NIV): one control strategy (traditional online continuing medical education) and two novel strategies (interprofessional education and just-in-time education).
详细描述
During a one-month intervention period, the investigators will pilot test the educational strategies in three participating UPMC ICUs. Prior to receiving education, participants will be invited to complete a short online survey. Participants in the control group will be invited to complete a 30-minute online continuing education module, which will conclude with a survey. Participants in the interprofessional education group will be invited to attend a 90-minute, in-person, interprofessional education session that will occur in or near the participating ICU. A trained advance practice provider will provide participants in the just-in-time education group with 5-10 minutes of education in the ICU when the ICU team is rounding on a patient who is identified to be high risk for extubation failure. The just-in-time education may occur more than once per day, depending on the number of high-risk patients identified. All educational strategies will include content on the benefits of preventive post-extubation NIV, the indications and contraindications for preventive post-extubation NIV, and the value of working together as an interprofessional ICU team when implementing preventive post-extubation NIV. Each educational intervention will include a survey designed to determine the feasibility, acceptability, and preliminary impact of the educational strategies. The investigators will also directly observe instances of interprofessional and just-in-time education and conduct in-person interviews to assess these factors in a qualitative manner. Lastly, during the intervention period and the 6 months before and after the intervention period, the investigators will collect data from the electronic health record and analyze changes in percent of high-risk patients who receive preventive post-extubation NIV, reintubation rate, duration of mechanical ventilation, ventilator-associated pneumonia, and in-hospital mortality.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 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
- 是
入选标准
- 未提供
排除标准
- 未提供
结局指标
主要结局
Number of ICU Team Members (Learners) Who Received Education
时间窗: Up to 1 month
This implementation outcome measuring reach only applies to learner participants.
Learner Attitudes Regarding Education (Mean Scores on Relevant Survey Questions)
时间窗: Up to 10 weeks
Using a 5-point Likert scale (1=strongly disagree; 5=strongly agree), learners reported their level of agreement with the statement "I liked the way the information was presented." This outcome only applies to learner participants.
次要结局
- Learner Specialization (Mean Scores on Relevant Survey Questions)(Up to 10 weeks)
- Learner Role Clarity (Mean Scores on Relevant Survey Questions)(Up to 10 weeks)
- Learner Psychological Safety (Mean Scores on Relevant Survey Questions)(Up to 10 weeks)
- Number of High-risk Patients Without Contraindications Who Received Post-extubation Noninvasive Ventilation(Participants will be followed for the duration of their hospital admission, estimated to be 1-2 weeks)
- Learner Credibility (Mean Scores on Relevant Survey Questions)(Up to 10 weeks)
- Learner Coordination (Mean Scores on Relevant Survey Questions)(Up to 10 weeks)
- Learner Perspectives on Leader Inclusiveness (Mean Scores on Relevant Survey Questions)(Up to 10 weeks)
研究者
Timothy Girard, MD, MSCI
Associate Professor
University of Pittsburgh
