Cluster-Randomized Trial of Air Filtration and Ventilation to Reduce Covid19 Spread in Homes
A Cluster-randomized Controlled Trial of Air Filtration and Ventilation Improvements to Reduce SARS CoV 2 Transmission Among Household Contacts
2 other identifiers
interventional
214
1 country
2
Brief Summary
Investigators are evaluating whether an intervention consisting of box-fans with MERV 16 filters ("filtration fans") and recommendations for improving ventilation in the home can reduce secondary spread of Covid19 from an index case to susceptible contacts within the home.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable covid19
Started Jan 2023
Longer than P75 for not_applicable covid19
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 30, 2023
CompletedFirst Submitted
Initial submission to the registry
March 18, 2023
CompletedFirst Posted
Study publicly available on registry
March 21, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 30, 2025
CompletedFebruary 19, 2026
February 1, 2026
2.9 years
March 18, 2023
February 17, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Incidence of Covid19
Investigators will measure the incidence of Covid19 in susceptible contacts on day 7.
7th day since enrollment in the trial
Secondary Outcomes (2)
Incidence of new upper respiratory symptoms
7th day since enrollment in the trial
Average CO2 levels
7 days
Study Arms (2)
Control
NO INTERVENTIONNo intervention will be administered in this arm. Investigators will give families a CO2 monitor to measure average CO2 levels in the home. Investigators will provide a link to the basic CDC isolation guidelines which would be part of standard of care. Investigators will test family members at day 0-1 for baseline testing; and again on day 7 for assessing secondary transmission among susceptible contacts.
Intervention
EXPERIMENTALFamilies are provided with one filtration fan unit per room in their home (and one for the index case; if the family lives in a studio, they would receive 2 units). Investigators will advise families on ventilation improvements in their home. Investigators will provide an instructional pamphlet that describes how the fans work and the importance of ventilation. Investigators will follow-up on day 3-4 to check in and run through a checklist to ensure the fans are working and ventilation improvements are being attempted. Investigators will give families a CO2 monitor to measure average CO2 levels in the home. Investigators will test family members at day 0-1 for baseline testing; and again on day 7 for assessing secondary transmission among susceptible contacts.
Interventions
Investigators are using box fans with attached MERV16 filters, a design that has been tested and published in the scientific literature.
The pamphlet has information on how the filtration fans work through visual images; and images of ventilation improvements in the home through opening windows.
On day 3-4 of the study, the study coordinator assigned to the house will call and check in regarding the filtration fan usage and remind families about the importance of filtration and ventilation.
Eligibility Criteria
You may qualify if:
- Household members live in a shared space (apartment, home) with others (as opposed to renting single rooms in a shared space, for example)
- At least 3 other people live in the household aside from index case
You may not qualify if:
- If index case test positive day was over 2 days prior
- If half or more household members are thought to be infected already
- If household has fewer than 3 contacts interested in participating in the study
- If fewer than 3 contacts are expected to be present in the house for a majority of the following 7 days
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
San Mateo Medical Center
San Mateo, California, 94403, United States
Stanford University Medical Center
Stanford, California, 94305, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Yvonne Maldonado, MD
Stanford University
- PRINCIPAL INVESTIGATOR
Abraar Karan, MD
Stanford University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Post-Doctoral Fellow
Study Record Dates
First Submitted
March 18, 2023
First Posted
March 21, 2023
Study Start
January 30, 2023
Primary Completion
December 30, 2025
Study Completion
December 30, 2025
Last Updated
February 19, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share