跳至主要内容
临床试验/NCT07348081
NCT07348081招募中不适用

Real World Evidence to Assess the Value of a Digital Care Coordination and Monitoring Program for Supporting Caregivers of Adults Discharged From the Emergency Department.

Fondation Hôpital Saint-Joseph1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2025年12月12日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
100
试验地点
1
主要终点
Change in the score on the 12-item Zarit Burden Interview questionnaire (ZBI-12, Appendix 1), measured on days 0, 30, and 90, among family caregivers participating in the study.

研究概览

简要总结

The RW-HOMECARE study is a prospective, longitudinal, real-world pilot trial designed to assess the impact of proposing the Monka digital solution to non-professional caregivers of patients discharged from emergency or short-stay units. The primary objective is to measure changes in caregiver burden using the ZBI-12 scale at baseline, 30 days, and 90 days. Secondary objectives include evaluating caregivers' physical and mental quality of life (SF-12), patient frailty (Clinical Frailty Scale), and the incidence of adverse events such as emergency visits, unplanned hospitalizations, falls, institutionalization, and death within 90 days. The study also examines the usability, acceptability, and satisfaction with Monka digital solution through standardized questionnaires, the correlation between algorithm-generated vulnerability scores and established measures, and reasons for non-adoption.

Eligible dyads (patient and caregiver) are recruited at discharge from emergency or short-stay units. After informed consent, caregivers receive free access to Monka digital solution for 3 months, along with a user guide. Follow-up assessments are conducted by phone at Day 30 and Day 90 (±14 days). All interventions by the coordinating nurse are tracked and analyzed quantitatively and qualitatively.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
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

  • FOR THE PATIENT
  • Person aged 18 or over, treated in the Emergency Department or Emergency Beds
  • Affiliated with Social Security
  • Having an adult non-professional relative helping them with one or more activities of daily living
  • Having a medical decision to return home within the next 72 hours
  • Who has given their free, informed, and express consent FOR THE CAREGIVER
  • Individuals aged 18 or older
  • Who are non-professional caregivers as defined in Article L. 113-1-3 of the Social Action and Families Code, living with or separately from the person being cared for (20)
  • Providing assistance to the patient with one or more activities of daily living, i.e., shopping, medical appointments, coordination of care, administrative tasks, and moral support
  • Access to a cell phone, computer, or tablet with an internet connection
  • Having given their free, informed, and express consent

排除标准

  • FOR THE PATIENT
  • Non-French speakers
  • People living in a medical institution or scheduled for institutionalization within the next 3 months
  • People receiving home hospitalization (HAD) or palliative care at home
  • People under legal protection, deprived of their liberty, or under legal guardianship (tutelage or curatelle) FOR THE CAREGIVER
  • Non-French speakers
  • People with cognitive or psychiatric disorders that prevent them from understanding and using the MONKA solution
  • People under legal protection, deprived of their liberty, or under legal guardianship (tutelage or curatelle)

研究组 & 干预措施

Patient and caregiver dyad experiencing the MyMonka solution in real-life conditions

Experimental

干预措施: Caregivers supporting vulnerable patients and using the MyMonka solution. (Other)

结局指标

主要结局

Change in the score on the 12-item Zarit Burden Interview questionnaire (ZBI-12, Appendix 1), measured on days 0, 30, and 90, among family caregivers participating in the study.

时间窗: Days 0, 30 and 90

次要结局

  • Change in the physical and mental quality of life of caregivers, expressed as the difference between SF-12 questionnaire scores at baseline, on day 30, and on day 90.(Days 30 and 90)
  • Change in patient frailty expressed as the difference between the Clinical Frailty Scale score obtained at inclusion and on day 90.(Days 0 and 90)
  • Percentage of people affected by the following adverse events within three months of returning home: new emergency room visits, unscheduled hospitalizations and their duration, falls, home hospitalizations, institutionalization, and death.(Days 90)
  • Evaluation of the use, acceptability, usability, and impact of the Monka digital solution for caregivers through intervention tracking, algorithm-based vulnerability assessment, and standardized questionnaires over a 90-day period.(Days 0 and 90)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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