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临床试验/NCT07399379
NCT07399379已完成不适用

Implementation of an Augmented Reality System to Complement Discharge Information in Hospitalized Cardiology Patients

Hospital Universitario Getafe1 个研究点 分布在 1 个国家目标入组 303 人开始时间: 2024年2月23日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
303
试验地点
1
主要终点
PRIMARY OUTCOME: PREM and treatment adherence at one and six months

研究概览

简要总结

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.

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
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

  • No access to a mobile device.
  • Untreated visual or hearing impairments that prevent viewing or understanding the videos.
  • Inability to understand Spanish

研究组 & 干预措施

Intervention Group

Active Comparator

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.

干预措施: Augmented reality app (Device)

Control group

No Intervention

This group receives the usual medical discharge report.

结局指标

主要结局

PRIMARY OUTCOME: PREM and treatment adherence at one and six months

时间窗: 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.

次要结局

  • MACE at one and six months(From enrollment at one and six months)

研究者

发起方
Hospital Universitario Getafe
申办方类型
Other
责任方
Sponsor

研究点 (1)

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