BridgeMD
New treatment option for ICU Acquired Weakness
Official title ICU-Recover Box 2.0, Smart Technology for Home Monitoring of ICU Patients
ClinicalTrials.gov ID: NCT07162948
What this study is testing
- What it's testing
- Smart technology could improve quality of care in patients who have been admitted to the ICU and have been discharged from ICU and hospital, by early diagnosis of complications and early (ambulatory) treatment. With the ICU-Recover Box and its smart technology the investigators see new opportunities to improve patient health and to recognize early if escalation of medical care is needed.
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
- Patient has been admitted to the ICU of the LUMC for \> 24 hours.
- Patient has received mechanical ventilation.
- Patient masters the English or Dutch language.
- Patient is able to use smart technology at home. (i.e. Wi-Fi available, sufficient comprehension of smart technology).
- Patient can be contacted and informed about the ICU-Recover box on one of the clinical wards of the LUMC.
You likely can't join if
- Patient is \< 18 years old.
- Patient is pregnant.
- Patient breastfeeds during the course of the study.
- Patient is discharged for palliative care.
- Patient is considered an incapacitated adult.
- Patient is unwilling to sign the informed consent form.
See the full eligibility criteria
- Patient has been admitted to the ICU of the LUMC for \> 24 hours.
- Patient has received mechanical ventilation.
- Patient masters the English or Dutch language.
- Patient is able to use smart technology at home. (i.e. Wi-Fi available, sufficient comprehension of smart technology).
- Patient can be contacted and informed about the ICU-Recover box on one of the clinical wards of the LUMC.
- Patient is discharged from a ward within the LUMC to home or an extra-hospital facility.
- Patient is \< 18 years old.
- Patient is pregnant.
- Patient breastfeeds during the course of the study.
- Patient is discharged for palliative care.
- Patient is considered an incapacitated adult.
- Patient is unwilling to sign the informed consent form.
- Patient is discharged to another hospital.
The study team makes the final eligibility decision.
Where it's taking place
- Leiden, South Holland, Netherlands
Compensation & support
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
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 Leiden, South Holland, Netherlands. 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.