Study Assessing the Effectiveness of a Cardiac Web-based eLearning Platform (eEduHeart I)

Hasselt University

Status: Completed

Conditions: Coronary Artery Disease

Treatments: Other: Control group; Other: Intervention group

Study type: Interventional

Funder types: Other

Identifiers

NCT02475967

PDEN-IFRE 01

Details and patient eligibility

About

In the trial cardiac patients will be provided with unrestricted access to the web-based eLearing platform for a one-month period.

Full description

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.

Enrollment: 1,000 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients suffering from coronary artery disease for which they are treated conservatively, with a percutaneous coronary intervention or with coronary artery bypass grafting

Exclusion criteria

• 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

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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1,000 participants in 2 patient groups

Intervention group

Experimental group

Description:

The intervention group patients have access to the eLearning platform in addition to conventional cardiac care.

Treatment:

Other: Intervention group

Control group

Active Comparator group

Description:

The control group patients receive conventional cardiac care alone.

Treatment:

Other: Control group