About this trial
The purpose of this research is to assess whether integration of an aerosol biosensor and air quality risk assessment software that integrates into a building management system will improve indoor air quality metrics in hospital environments and reduces risk factors associated with respiratory disease transmission.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Mayo Clinic Staff working in ED with a minimum of .7 FTE in Midwest (MN and WI), Phoenix (AZ), or Jacksonville (FL) and patient contact.
Mayo Clinic Staff working in primary care with a minimum of .7 FTE. in Rochester (MN), Phoenix (AZ), or Jacksonville (FL) and patient contact
Disqualifiers
Any participant who does not meet either of the inclusion criteria.
Trial design
Single group
Treatments tested in this trial
Self-swab test
Diagnostic testParticipants will self-report when they are experiencing respiratory symptoms and will be asked for a self-swab to be used for data analysis.
Treatment groups
Trial outcomes
Primary outcomes
Number of participants to experience acute respiratory infection (ARI) symptoms
Symptoms include: at least 2 upper respiratory symptoms for at least 24 hours; OR at least 2 symptoms that include an upper/lower respiratory symptom and a systemic symptom (fever, fatigue, body aches, headache, decreased appetite) for at least 24 hours
Secondary outcomes
Number of confirmed cases of acute respiratory infections
Number of cases confirmed by at least one viral panel-positive swab detected by RT-PCR
Number of confirmed cases of lower respiratory tract disease
Number of cases of lower respiratory tract disease confirmed by at least one viral panel-positive swab detected by RT-PCR
Sponsors and contacts
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Mayo Clinic
Lead sponsor
Advanced Research Projects Agency for Health
Collaborator
Roche Pharma AG
Collaborator
This trial is not recruiting at the moment. You can still explore other options: