Personalized Video-based Education for Chronic Stroke Survivors: A Randomized Clinical Trial
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- Patient satisfaction with stroke education (90 days)
研究概览
简要总结
This is a single-center randomized control trial assessing the impact of a personalized video-based educational platform on patients satisfaction and stroke knowledge in the context of chronic stroke.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •History of ischemic stroke between 1 and 10 years prior to enrollment
- •Receiving outpatient stroke care at the Hospital of the University of Pennsylvania
- •At least 18 years old
- •Access to a smart phone, tablet, or computer
- •Willingness to complete 2 follow-up surveys (7 days and 90 day post-enrollment)
排除标准
- •Unwilling or unable to access the customized app with a smartphone, tablet, or computer
- •Complete dependence on caregiver for all activities of daily living
- •Stroke occurred less than 1 year or greater than 10 years prior to screening/enrollment
- •Patient has severe aphasia (score of greater than or equal to 2 on National Institutes of Health Stroke Scale item 9)
研究组 & 干预措施
Standard Education
Standard stroke patient education as per the medical providers
MyStroke
Access to a personalized video-based stroke educational platform
干预措施: MyStroke (Behavioral)
结局指标
主要结局
Patient satisfaction with stroke education (90 days)
时间窗: 90 days
5-point Likert-scale (Q: I am satisfied with the quality of my stroke education; Answers range from strongly disagree to strongly agree)
Stroke risk factor recognition (90 days)
时间窗: 90 days
The proportion of patients who correctly identify at least one of their vascular risk factors
Stroke etiology recognition (90 days)
时间窗: 90 days
The proportion of patients who correctly identify their stroke etiology
次要结局
- Stroke patient education retention (SPER) survey (90 days)(90 days)
- Patient satisfaction with stroke education (7 days)(7 days)
- Stroke etiology recognition (7 days)(7 days)
- Stroke patient education retention (SPER) survey (7 days)(7 days)
- Stroke prevention medication recognition (90 days)(90 days)
- Stroke prevention medication recognition (7 days)(7 days)
- EuroQOL - visual analog scale (7 days)(7 days)
- Medication adherence (7 days)(7 days)
- Stroke risk factor recognition (7 days)(7 days)
- EuroQOL - visual analog scale (90 days)(90 days)
- modified Rankin Scale(90 days)
- Medication adherence (90 days)(90 days)
研究者
Christopher Favilla
Assistant Professor of Neurology
University of Pennsylvania