Digital Intervention for Healthcare Workers
2026年8月27日 更新者：University of Illinois at Chicago
Enhancing Sustained Engagement in Digital Mental Health Interventions (DMHIs)
The goal of this clinical trial is to test which engagement strategies lead to more participation in a digital mental health program among healthcare workers. The main questions it aims to answer is:
- Does content tailoring increase engagement with the digital program?
- Does human support increase engagement with the digital program?
Researchers will compare the general intervention to a tailored intervention and to the tailored intervention with human support coaching to see what leads to more engagement with/use of the program.
Participants will:
- Use a digital program weekly for 6 weeks
- Complete questionnaires at 5 times: Start of study, Week 2, Week 3 (mid-program), Week 6 (end of program), and Week 10 (follow-up)
研究概览
研究类型
介入性
注册 (估计的)
201
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息，以及有关进行该研究的地点的信息。
学习联系方式
- 姓名：Jennifer Duffecy, PhD
- 电话号码：312-413-1225
- 邮箱：jduffecy@uic.edu
学习地点
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Illinois
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Chicago、Illinois、美国、60612
- Neuropsychiatric Institute
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接触：
- Jennifer Duffecy, PhD
- 电话号码：312-413-1225
- 邮箱：jduffecy@uic.edu
-
-
参与标准
研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
不
描述
Inclusion Criteria:
- Age 18 years or older, all sexes
- Currently working in healthcare in the US with at least 4 hours per week of direct patient contact
- Stable access to internet
- Have a total score between 3-14 on the PHQ-9 (Patient Health Questionnaire-9), suggestive of mild to moderate depressive symptoms
Exclusion Criteria:
- Have a total score of ≥15 on the PHQ-9, indicating Severe Depressive symptoms.
- Currently diagnosed with a psychotic disorder or bipolar disorder, based on self-report.
- Currently receiving psychotherapy for depression or anxiety based on self-report; If on medications for depression or anxiety, must be on a stable dose of medication for at least 2 weeks.
学习计划
本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。
研究是如何设计的？
设计细节
- 主要用途：预防
- 分配：随机化
- 介入模型：阶乘赋值
- 屏蔽：无（打开标签）
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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有源比较器：Control Group
Infographic onboarding and the Cognitive Behavioral Therapy (CBT)-based 6-week digital mental health intervention.
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The digital mental health intervention is based on Cognitive Behavioral Therapy principles and consists of learning modules covering basic skills (e.g., behavioral activation) and interactive tools to assist in learning and implementing the skills associated with the learning modules.
Interactive tools are designed to support implementation of cognitive behavioral skills including activity scheduling and monitoring, cognitive restructuring, goal setting, relaxation, and mood tracking.
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实验性的：Content Tailoring Group
Healthcare-worker-tailored infographic onboarding and the Cognitive Behavioral Therapy (CBT)-based 6-week digital mental health intervention with healthcare worker tailoring.
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The digital mental health intervention is based on Cognitive Behavioral Therapy principles and consists of learning modules covering basic skills (e.g., behavioral activation) and interactive tools to assist in learning and implementing the skills associated with the learning modules.
Interactive tools are designed to support implementation of cognitive behavioral skills including activity scheduling and monitoring, cognitive restructuring, goal setting, relaxation, and mood tracking.
This version of the intervention contains content tailored specifically for healthcare workers, based on findings from a co-design, qualitative focus group process.
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实验性的：Content Tailoring Plus Human Support Group
An onboarding engagement call with a human coach and the Cognitive Behavioral Therapy (CBT)-based 6-week digital mental health intervention with healthcare worker tailoring, plus human support via messaging (coaching).
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The digital mental health intervention is based on Cognitive Behavioral Therapy principles and consists of learning modules covering basic skills (e.g., behavioral activation) and interactive tools to assist in learning and implementing the skills associated with the learning modules.
Interactive tools are designed to support implementation of cognitive behavioral skills including activity scheduling and monitoring, cognitive restructuring, goal setting, relaxation, and mood tracking.
This version of the intervention contains content tailored specifically for healthcare workers, based on findings from a co-design, qualitative focus group process.
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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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Engagement with the intervention (subjective)
大体时间：From start of intervention to end of intervention period at 6 weeks.
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The primary outcome is engagement with intervention.
Subjective engagement will be measured via the TWente Engagement with Ehealth Technologies Scale (TWEETS), a 9-item measure aimed at assessing behavioral engagement, cognitive engagement, and affective engagement.
A higher total score reflects a greater, more positive engagement with the digital health intervention.
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From start of intervention to end of intervention period at 6 weeks.
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Engagement - Number of Lessons
大体时间：From start of intervention to end of intervention period at 6 weeks.
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An objective measure of engagement with the digital intervention is number of lessons read (i.e., module completion).
More lessons read reflects more engagement with the intervention.
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From start of intervention to end of intervention period at 6 weeks.
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Engagement - Number of Tools
大体时间：From start of intervention to end of intervention period at 6 weeks.
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An objective measure of engagement with the digital intervention is number of tools completed (i.e., tool usage).
More tools completed reflects more engagement with the intervention.
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From start of intervention to end of intervention period at 6 weeks.
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Engagement - Duration of Time
大体时间：From start of intervention to end of intervention period at 6 weeks.
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An objective measure of engagement with the digital intervention is the duration of time participants spend on the digital intervention site.
More time on the site reflects more engagement with the intervention.
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From start of intervention to end of intervention period at 6 weeks.
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Burnout
大体时间：From baseline to follow-up at 10 weeks.
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Burnout is measured via the Oldenburg Burnout Inventory, a validated 16-item survey with positively and negatively framed items that cover 2 areas: exhaustion (physical, cognitive, and affective aspects) and disengagement from work (negative attitudes toward work objects, work content, or work in general).
Scores on the Oldenburg Burnout Inventory can be presented as an overall total (range 16 to 64).
Higher total scores indicate a higher level of burnout.
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From baseline to follow-up at 10 weeks.
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Depressive Symptoms
大体时间：From baseline to follow-up at 10 weeks.
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Depressive symptoms are measured via the Patient Health Questionnaire (PHQ-9), a validated 9-item multipurpose instrument for screening, monitoring, and measuring depression, asking participants to rate their frequency of DSM symptoms over the past 2 weeks.
PHQ-9 scores are obtained by adding score for each question (total points).
Total scores of 5, 10, 15, and 20 represent cut-points for mild, moderate, moderately severe and severe depression, respectively.
Higher scores reflect more depressive symptoms.
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From baseline to follow-up at 10 weeks.
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Anxiety symptoms
大体时间：From baseline to follow-up at 10 weeks.
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The Generalized Anxiety Disorder Screener (GAD-7) is a validated 7-item practical self-report anxiety questionnaire, asking participants to rate their frequency of symptoms over the past 2 weeks.
GAD-7 score obtained by adding score for each question (total points).
Total scores of 5, 10, and 15 represent cut-points for mild, moderate, and severe anxiety.
Higher scores reflect more anxiety.
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From baseline to follow-up at 10 weeks.
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (估计的)
2026年11月1日
初级完成 (估计的)
2028年1月1日
研究完成 (估计的)
2028年3月1日
研究注册日期
首次提交
2026年8月24日
首先提交符合 QC 标准的
2026年8月27日
首次发布 (实际的)
2026年8月28日
研究记录更新
最后更新发布 (实际的)
2026年8月28日
上次提交的符合 QC 标准的更新
2026年8月27日
最后验证
2026年8月1日
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- 2025-0594
- UM1TR005438 (美国 NIH 拨款/合同)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)？
不
药物和器械信息、研究文件
研究美国 FDA 监管的药品
不
研究美国 FDA 监管的设备产品
不
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