Interprofessional Group Intervention to Promote Faculty Wellbeing and Engagement
研究概览
详细说明
To test the hypothesis that an intervention involving self-facilitated interprofessional group meetings would result in improvement in wellbeing and to determine whether use of a written curriculum provided increased benefit, the following study is conducted:
Practicing clinical faculty in the Department of Obstetrics and Gynecology at the Massachusetts General Hospital were recruited to participate in three monthly small groups over dinner. Participants were randomized to a control group, which met without any specified guidelines for discussion content, or to receive an intervention which consisted of a one-page discussion guide addressing themes relevant to challenges in the healthcare environment: reframing challenging patient interactions; embracing uncertainty in work; and coping with errors, near misses, and bad outcomes. Outcomes included burnout, empowerment and engagement in work, stress from uncertainty assessed using validated metrics, and perception of of collegiality and community.
All participants were also offered the option of participating in evaluation of biomarkers. To test the hypothesis that an increased sense of bonding and relational connection, and reduced stress levels would be reflected by changes in hormone levels during the meeting and over the course of the study. Faculty who opted into this portion of the study gave the following samples:
Urine Oxytocin before and after the first and third group meetings Salivary Oxytocin before and after the first and third group meetings Salivary Cortisol before and after the first and third group meetings Hair Cortisol at the beginning of the study and at the end of the study (a roughly three month interval).
An optional focus group was conducted after the three monthly sessions.
All participants signed a consent form prior to participating in the study.
研究类型
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
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Massachusetts
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Boston、Massachusetts、美国、02114
- Massachusetts General Hospital
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参与标准
资格标准
适合学习的年龄
- 孩子
- 成人
- 年长者
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Physican in the Department of Obstetrics and Gynecology at Massachusetts General Hospital
- Nurse Practitioner in the Department of Obstetrics and Gynecology at Massachusetts General Hospital
- Certified Nurse Midwife in the Department of Obstetrics and Gynecology at Massachusetts General Hospital
Exclusion Criteria:
- None
学习计划
研究是如何设计的?
设计细节
- 主要用途:其他
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:Intervention
Providers were placed in small groups and given the intervention of a discussion guide to facilitate discussion.
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Written list of prompts to facilitate discussion
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无干预:Control
Providers were placed in small groups and not given a discussion guide to facilitate discussion.
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Burnout
大体时间:Change over the three month study period. Baseline measurement and immediately after final intervention.
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Change from baseline in 2 item Maslach Burnout Inventory scores before and after the intervention. Minimum score: 2; Maximum score: 14 Higher score = more burnt out (worse outcome) |
Change over the three month study period. Baseline measurement and immediately after final intervention.
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Stress from Uncertainty
大体时间:Change over the three month study period. Baseline measurement and immediately after final intervention.
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Change in scores on Physician Response to Uncertainty Scale before and after intervention Minimum score: 6; Maximum score: 90 Higher score = increased stress due to uncertainty (worse outcome)
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Change over the three month study period. Baseline measurement and immediately after final intervention.
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Work Engagement
大体时间:Change over the three month study period. Baseline measurement and immediately after final intervention.
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Change in scores on Utrecht Work Engagement Scale before and after intervention Minimum score: 0; Maximum score: 54 Higher score = higher engagement at work (better outcome)
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Change over the three month study period. Baseline measurement and immediately after final intervention.
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Urine oxytocin
大体时间:Two samples were taken one hour apart at baseline, and this was repeated three months later.
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Change from baseline in the level of urine oxytocin before and after each intervention.
This is an exploratory study so the maximum and minimum values are not known, and any change up or down is interesting.
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Two samples were taken one hour apart at baseline, and this was repeated three months later.
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Salivary Oxytocin
大体时间:Two samples were taken one hour apart at baseline, and this was repeated three months later
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Change from baseline in the level of salivary oxytocin before and after each intervention.
This is an exploratory study so the maximum and minimum values are not known, and any change up or down is interesting.
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Two samples were taken one hour apart at baseline, and this was repeated three months later
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Salivary Cortisol
大体时间:Two samples were taken one hour apart at baseline, and this was repeated three months later
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Change from baseline in the level of salivary cortisol before and after each intervention.
This is an exploratory study so the maximum and minimum values are not known, and any change up or down is interesting.
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Two samples were taken one hour apart at baseline, and this was repeated three months later
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Hair Cortisol
大体时间:Change over the three month study period. Baseline measurement and immediately after final intervention.
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Change from baseline in hair cortisol levels.
Maximum and minimum levels are not known and any change up or down is interesting.
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Change over the three month study period. Baseline measurement and immediately after final intervention.
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Work Empowerment Scale
大体时间:Change over the three month study period. Baseline measurement and immediately after final intervention.
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Minimum score: 12; Maximum score: 84 Change from baseline on Work Empowerment Scale before and after intervention.
Higher score = higher empowerment at work (better outcome)
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Change over the three month study period. Baseline measurement and immediately after final intervention.
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合作者和调查者
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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