Implementation of an Augmented Reality System to Complement Discharge Information in Hospitalized Cardiology Patients
Overview
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Hospital Universitario Getafe
- Enrollment
- 303
- Locations
- 1
- Primary Endpoint
- PRIMARY OUTCOME: PREM and treatment adherence at one and six months
Overview
Brief Summary
The goal of this clinical trial is to find out whether a simple augmented reality tool provided at hospital discharge can improve patients' understanding of their care, adherence to treatment, and health outcomes, compared with the usual discharge information.
This study includes adult patients who are admitted to a cardiology department because of:
- Ischaemic heart disease
- Atrial fibrillation
- Heart failure
- Or who need a pacemaker implantation
The main questions this study aims to answer are:
- Does providing augmented reality information at discharge improve patients' perceived quality of care?
- Does it improve patients' adherence to their prescribed treatment?
- Does it reduce major cardiovascular events such as hospital readmission, heart attack, stroke, or cardiovascular death?
Researchers will compare two groups of participants:
- A control group, who will receive the usual medical discharge report.
- An intervention group, who will receive the usual medical discharge report plus an information card with a drawing and a QR code that gives access to an augmented reality application.
Participants will:
- Receive their discharge information according to the group they are assigned to.
- Use the augmented reality application if they are in the intervention group.
- Be followed over time to assess treatment adherence, patient experience, and cardiovascular events.
This is a low-intervention, randomized, single-centre clinical trial conducted in Getafe, Madrid, Spain. Participation in this study does not involve taking any additional medication.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Participants must have access to a mobile device (such as a smartphone or tablet).
- •Participants must have been admitted to the Cardiology Department of Getafe University Hospital for ischemic heart disease, heart failure, atrial fibrillation, or pacemaker implantation.
Exclusion Criteria
- •No access to a mobile device.
- •Untreated visual or hearing impairments that prevent viewing or understanding the videos.
- •Inability to understand Spanish
Arms & Interventions
Intervention Group
This group receives the usual medical discharge report plus an information card with a drawing and a QR code that gives access to an augmented reality application explaining their disease.
Intervention: Augmented reality app (Device)
Control group
This group receives the usual medical discharge report.
Outcomes
Primary Outcomes
PRIMARY OUTCOME: PREM and treatment adherence at one and six months
Time Frame: Follow up at one and six months from enrollment
To assess PREM (Patient-Reported Experience Measures) in the intervention group and in the control group at discharge and at follow-up.
Secondary Outcomes
- MACE at one and six months(From enrollment at one and six months)