eEduHeart I: a Multi-center Randomized, Controlled Trial Investigating the Effectiveness of a Cardiac Web-based eLearning Platform
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 1,000
- 试验地点
- 2
- 主要终点
- Health-related quality of life
研究概览
简要总结
In the trial cardiac patients will be provided with unrestricted access to the web-based eLearing platform for a one-month period.
详细描述
Patients participating in the trial will be provided with a cardiac web-based eLearning platform for one month during study period. The medical content of the packages will be gathered from a multidisciplinary input of both medics (e.g. cardiologists) and paramedics (e.g. psychologists).
E-Learning packages type I: videos with information from caregivers. In these videos, medics and paramedics are interviewed to highlight the etiology, pathophysiology and treatment of coronary artery disease; the associated comorbidities and the ways to prevent recurrence.
E-Learning packages type II: videos in which patients are interviewed. Patients can help each other to adhere to their treatment plan, by sharing stories from their own experience about their illness and the rehabilitation afterwards. Short clips of maximum 2 minutes will be provided to study participants.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Single (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
- •Patients suffering from coronary artery disease for which they are treated conservatively, with a percutaneous coronary intervention or with coronary artery bypass grafting
排除标准
- •Patients with dementia or cognitive impairment not being able to sufficiently understand the E-Learning packages content
- •(Foreign) patients unable to speak Dutch, thereby not being able to understand the content of the E-Learning packages
- •Patients with advanced visual and/or auditory impairments, hindering them to adequately understand the E-earning packages
- •Patients participating in another trial during the Pilot study period
- •Patients refusing to provide signed consent
研究组 & 干预措施
Intervention group
The intervention group patients have access to the eLearning platform in addition to conventional cardiac care.
干预措施: Intervention group (Other)
Control group
The control group patients receive conventional cardiac care alone.
干预措施: Control group (Other)
结局指标
主要结局
Health-related quality of life
时间窗: 3 months
Health-related quality of life, assessed by HeartQol
次要结局
- Adherence to the E-learning packages(3 months)
- Effectiveness of E-learning packages(3 months)
- User experience of eLearning platform(3 months)
研究者
prof. dr. Paul Dendale
prof. dr.
Hasselt University