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Official title 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.
ClinicalTrials.gov ID: NCT07348081
What this study is testing
- What it's testing
- 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.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- 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
You likely can't join if
- 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
See the full eligibility criteria
- 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
- 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)
The study team makes the final eligibility decision.
Where it's taking place
- Paris, France
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Paris, France. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.