NCT05777720

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
214

participants targeted

Target at P50-P75 for not_applicable covid19

Timeline
Completed

Started Jan 2023

Longer than P75 for not_applicable covid19

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 30, 2023

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

March 18, 2023

Completed
3 days until next milestone

First Posted

Study publicly available on registry

March 21, 2023

Completed
2.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2025

Completed
Last Updated

February 19, 2026

Status Verified

February 1, 2026

Enrollment Period

2.9 years

First QC Date

March 18, 2023

Last Update Submit

February 17, 2026

Conditions

Keywords

ventilationair filtrationCovid19SARS CoV 2household transmission

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 INTERVENTION

No 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

EXPERIMENTAL

Families 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.

Device: Filtration FanBehavioral: Safe-home pamphletBehavioral: Mid-week phone call

Interventions

Investigators are using box fans with attached MERV16 filters, a design that has been tested and published in the scientific literature.

Intervention

The pamphlet has information on how the filtration fans work through visual images; and images of ventilation improvements in the home through opening windows.

Intervention

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.

Intervention

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

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

Location

Stanford University Medical Center

Stanford, California, 94305, United States

Location

MeSH Terms

Conditions

COVID-19Respiratory Aspiration

Condition Hierarchy (Ancestors)

Pneumonia, ViralPneumoniaRespiratory Tract InfectionsInfectionsVirus DiseasesCoronavirus InfectionsCoronaviridae InfectionsNidovirales InfectionsRNA Virus InfectionsLung DiseasesRespiratory Tract DiseasesRespiration DisordersPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Yvonne Maldonado, MD

    Stanford University

    STUDY DIRECTOR
  • Abraar Karan, MD

    Stanford University

    PRINCIPAL INVESTIGATOR

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

Locations