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Early@home

Telemedicine for recovering COVID-19 patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON28634
Enrollment
62
Registered
2020-11-30
Start date
2021-01-11
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COVID-19

Interventions

Relocated hospital care with telemedicine

Sponsors

None
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - The patient is in the recovery phase of COVID-19 and receives low flow oxygen therapy or no oxygen therapy - The patient is 18 years of age or older; - The patient is admitted to the hospital with COVID-19 pneumonia; - The patient is expected to be discharged home; - A partner/primary caregiver is available at the patients home for support; - A rectal thermometer is available; - The patient is in possession of a smartphone with the ability to host the Luscii app; - The patient or the caregiver is able to use the smartphone and Luscii app; - The patient or the caregiver is able to use the pulse oximeter; - The patient or the caregiver is able to speak, read and understand the Dutch language sufficiently enough to be able to use the Luscii app;

Exclusion criteria

Exclusion criteria: - A patient with dementia or severe psychiatric disorder who is unlikely to be compliant to the intervention (to be determined by treating physician); - A patient who is discharged to a care facility or rehabilitation center; - A patient who needs more medical support than can be organized at home.

Design outcomes

Primary

MeasureTime frame
Days alive at home 30 days after randomization

Secondary

MeasureTime frame
- Mortality, in hospital and 30 days after randomization - COVID-19 specific mortality, in hospital and 30 days after randomization - Total hospital length of stay - Number of ED visits or unplanned outpatient clinic visits 30 days after randomization - Number of general practitioner visits 30 days after randomization - Number of hospital readmissions - Number of intensive care unit readmissions - Score for physchological wellbeing at start and discharge

Contacts

Public ContactHarriët van Goor

UMC Utrecht

h.m.r.vangoor-3@umcutrecht.nl0887567967

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)