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Telemonitoraggio Domiciliare Della Saturazione Arteriosa di Ossigeno in Pazienti COVID-19

Telemonitoraggio Domiciliare Della Saturazione Arteriosa di Ossigeno in Pazienti COVID-19

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05731583
Acronym
SATCoV
Enrollment
300
Registered
2023-02-16
Start date
2021-01-06
Completion date
2024-01-31
Last updated
2023-02-16

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

Conditions

COVID-19

Brief summary

The COVID-19 pandemic created an urgent need to implement digital health solutions for remote clinical management of infected patients who could be monitored at home. The Gemelli Polyclinic in Rome provided a digital health program (SATCOV) to monitor at home newly diagnosed COVID-19 patient, or after an early discharge from the COVID units. A digital application and a wireless oximeter were provided to patients. Oxygen saturation, heart rate and body temperature were monitored. The aim is to evaluate the feasibility and safety of the oxygen saturation telemonitoring in COVID-19 patients. Clinicians personalized their remote assistance defining specific alerts for each patient and/or required a timely hospitalization in a dedicated COVID unit if necessary.

Interventions

A digital application and a wireless oximeter were provided to both groups. Oxygen saturation, heart rate and (optional) body temperature were monitored at least twice a day.

Sponsors

Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* adult patients (age\>18) * confirmed diagnosis of Sars-CoV-2 infection by a positive nasopharyngeal and oropharyngeal swab (PCR or rapid test) * clinical condition compatible with hospital discharge (for recoving COVID group) or home management (for ongoing COVID group)

Exclusion criteria

* non-autonomous patients * patients without a smartphone and home internet connection * patients unable to refer to emergency room in less than 2 hours or unable to observe home isolation * the presence of severe comorbidities that could compromise the safety of telemonitoring

Design outcomes

Primary

MeasureTime frameDescription
Number of patients without missing days of telemonitoring/total patients14 daysNumber of patients without missing days of telemonitoring/total patients

Secondary

MeasureTime frameDescription
Oxygen saturation measurements14 daysNumber of oxygen saturation measurements performed/total measurements required by protocol
Number of subject hospitalized/total patients3 yarsNumber of subject hospitalized/total patients
Descriptive statistics14 daysGroups' description of their clinical and demographics characteristics
Correlation between the number of comorbidities and smoking status and SpO2 nadir14 daysCorrelation between the number of comorbidities and smoking status and SpO2 nadir
Cost efficacy14 daysCalculation of resources spent per patient

Countries

Italy

Contacts

Primary ContactLuca Richeldi, MD
luca.richeldi@policlinicogemelli.it+390630157852

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026