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临床试验/NCT06171763
NCT06171763已完成不适用

The Multi-stakeholder Assessment of Economic and Managerial Determinants and Impacts of Telemedicine: a Comparison Between a Tele-homecare Solution and Traditional Care Models.

Buzzi Children's Hospital1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2022年8月8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
150
试验地点
1
主要终点
Early discharge utilizing an user-friendly mobile medical device

研究概览

简要总结

The study aims to conduct a comprehensive evaluation involving multiple stakeholders to assess the factors influencing and the consequences of telehomecare in comparison to traditional care models. The integration of technology into the healthcare sector necessitates significant changes in care of patients, organizational structures, production processes, organizational responsibilities, and the management of service delivery processes.

The delivery of telemedicine services through integrated devices represents a method of service production that demands active involvement from patients or, in the case of pediatric patients, their caregivers. This collaborative process of patient engagement in healthcare services is referred to as "co-production." In this research, telehomecare will be examined as an illustrative instance of co-producing healthcare services.

Co-production implies that the inputs into a production process are contributed not only by the organization producing a good or service but also by the users. In the case study, co-production occurs through the interaction between patients/caregivers and professionals during telehealth visits for device-mediated monitoring activities. Throughout the televisit, patients/caregivers play a crucial role in collecting and sharing the necessary parameters with professionals using the device, thereby serving as essential actors in the care process.

The investigators explored the impact of a transitional care program, utilizing an user-friendly mobile medical device, to support an early discharges in a pediatric setting. Clinical outcome and economic advantages are considered. This study will contribute to implement knowledge on the role of telemedicine on HaH healthcare in pediatrics.

详细描述

This is a single-center, two-arm, randomized, open-label, parallel-group study that was conducted at Buzzi Children's Hospital, a hospital in a metropolis located in Milan (Italy). The different arms consisted of an experimental group with an early discharge adopting telehomecare and a standard care group with in-person physical care until the end of hospitalization.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Single (Participant)

入排标准

年龄范围
12 Months 至 18 Years(Child, Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Age: 0-18 years.
  • •Gender: Both males and females
  • •Patients: Hospitalized at the end of treatment.
  • •Stable Vital Signs (heart rate, respiratory rate, oxygen saturation)
  • •Stable/Improving/Resolved biochemical Tests.
  • •Absence of Fever
  • •Consent/Assent: Willingness to participate with appropriate consent or assent based on age.
  • •Proximity to Domicile: Residence within a maximum distance of 45 minutes.
  • •Adequate Home Facilities.
  • •Language Proficiency: Adequate knowledge of the Italian language.
  • •Possession of Compatible Device

排除标准

  • •Refusal to Participate
  • •Vital Signs Instability
  • •Presence of Fever
  • •Deteriorating biochemical Test Results
  • •Residence More Than 45 Minutes Away
  • •Inadequate Home Facilities
  • •Language Barrier
  • •Lack of a Compatible Device
  • •Not owning a device with an operating system suitable for supporting the Tytocare app.

研究组 & 干预措施

Telehome care

Experimental

For patients/caregivers assigned to the tele-homecare group, before discharge, instruction on the use of the TytoCareTM system was provided by healthcare personnel trained in the use of the system. Subsequently, each patient give the device they used until the scheduled post-discharge clinical assessment. A parent/caregiver was invited to participate for each pediatric patient.

Every 24 hours, the patient was assessed remotely in synchronous teleconsultation by medical staff; during tele-visit, the physician performed the complete routine procedure, including medical history and physical examination with user friendly medical device and completed the data collection sheet.

At 72 hours after discharge, an in-person clinical assessment was scheduled for outcome evaluation. In particular, during the visit, the complete resolution of the disease state was assessed through the post-discharge objective examination.

干预措施: Telemedicine (Other)

Standard care

No Intervention

Patients remained hospitalized for the continuation of the treatment. Every 24 hours, the patient was assessed in person by medical staff; the traditional physical examination involved assessment of the clinical parameters using standard equipment such as a digital thermometer, conventional stethoscope, and otoscope and completed the same data collection sheet.

After 72 hours of hospital observation, an in-person clinical examination was conducted to evaluate the outcome. In particular, during the visit, the complete resolution of the disease state was assessed through the post-discharge objective examination.

结局指标

主要结局

Early discharge utilizing an user-friendly mobile medical device

时间窗: 12 months

Considering in-person visit as the standard care procedure, the primary objective of this study is to obtain concordance with complete resolution of the disease from in-person physical care, without re-admission to the hospital. The investigators expect non-readmission in a minimum of 90 % of cases. Outcome measure: count and percentage of patients readmitted to the hospital after early discharge

次要结局

  • Length of stay(12 months)
  • Economic impact(12 months)

研究者

发起方
Buzzi Children's Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Valeria Calcaterra

Clinical Professor

Buzzi Children's Hospital

研究点 (1)

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