Telemedicine for recovering COVID-19 patients

Completed

Conditions: 10047438
COVID-19
10024970

Registration Number: NL-OMON49189

Lead Sponsor: niversitair Medisch Centrum Utrecht

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Completed

Sex: Not specified

Target Recruitment: 100

Inclusion Criteria

- The patient is admitted to the hospital with COVID-19 pneumonia;
- The patient is recovering;
- 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 (iOS or Android);
- 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

- 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 the caregivers or CaHS can
manage.

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The primary endpoint is the difference in number of days alive at home, 30 days<br /><br>from randomization. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Secondary endpoints are the difference in mortality, hospital length of stay,<br /><br>readmission to the hospital and to the ICU, number of unplanned visits to the<br /><br>hospital and number of visits to the general practitioner, and Hospital Anxiety<br /><br>and Depression Scale score after randomization and at discharge. </p><br>