COVID-19 Respiratory Infection Clinical Trial
— UVCinLTCsOfficial title:
Do Far-UVC Light Devices Reduce the Incidence of Influenza-Like Illnesses, Respiratory Illnesses, and COVID-19 Infections in Long-term Care Facilities?
Verified date | October 2021 |
Source | Nova Scotia Health Authority |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Elderly people who have multiple health problems are at higher risk of illness from viral respiratory infections, such as influenza (the flu) and COVID-19. This is especially true for residents in long-term care because the usual methods of infection control (handwashing, mask-wearing, and distancing) are difficult to enforce due to the memory problems of many residents and the frequently shared common spaces. It can also be difficult to prevent the spread of viral infections within long-term care because many residents are unable to tell their caregivers when they are feeling ill. Also, some elderly people do not show typical symptoms of infection (like fever), instead they may suddenly become confused or weak. This study will test if a safe form of ultraviolet light (far-UVC) can be effective as an extra method of disinfection (in addition to usual manual cleaning) against airborne and surface viruses that can cause respiratory infections.
Status | Enrolling by invitation |
Enrollment | 200 |
Est. completion date | April 30, 2023 |
Est. primary completion date | February 28, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility | Exclusion Criteria: LTC residents who do not consent to participate |
Country | Name | City | State |
---|---|---|---|
Canada | Northwood Halifax Campus | Halifax | Nova Scotia |
Canada | Windsor Elms Village | Windsor | Nova Scotia |
Lead Sponsor | Collaborator |
---|---|
Kenneth Rockwood | Department of Health, Nova Scotia, Nova Scotia Health Authority, Research Nova Scotia |
Canada,
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* Note: There are 18 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | A diagnosis of COVID-19 or other respiratory viral infection | Diagnosis will be based on positive laboratory finding of SARS-CoV-2, influenza A, influenza B, respiratory syncytial virus, or other respiratory viral infections (as per available testing). Testing will be performed on nasal swabs collected from participants who are positive for any of the symptoms in the screening protocol. | Over 2 flu seasons, approximately 24 months | |
Secondary | Time to recovery or death | Number of days from diagnosis of respiratory viral infection until recovery or death. Participant will be deemed "recovered" once their overall health status (vital, functional, and cognitive) has been stable for one week. This return to stable state will be determined by participant's clinical care team and is part of usual care. | From the date of diagnosis until the date of recovery or date of death, whichever comes first, assessed up to 30 days. |