ORegon CHild Absenteeism Due to Respiratory Disease Study - Air Surveillance
| Registry | NCT07298967 |
|---|---|
| Status | Suspended - for the summer, continue enrollment this fall |
| Phase | Not applicable |
| Study type | Interventional; na, single group, masking: none, basic science |
| Enrollment | 422 (Estimated) |
| Sponsor | University of Wisconsin, Madison (Other) |
| Conditions | Acute Respiratory Infection, Influenza-like Illness |
| Interventions | Nasal swab, Indoor air quality monitor (Diagnostic test, device) |
| Dates | start 2026-01-07, primary completion 2027-06-01 (estimated), completion 2027-06-01 (estimated), first posted 2025-12-23, last updated 2026-06-12 |
| Locations | 1 site in United States |
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All trials for Acute Respiratory Infection All trials for Influenza-like Illness All trials of Nasal swab All trials of Indoor air quality monitor
The purpose of this observational study is to compare the effectiveness of air surveillance and to better understand the relationship between household transmission and viruses detected in the air.
Participants will provide nasal swabs and have an air sample surveillance device installed in their home.
The purpose of ORCHARDS-AIR is to utilize air surveillance in participant homes in conjunction with individually collected nasal specimens to assess their concordance and evaluate the significance of airborne detection with household transmission of common respiratory pathogens such as influenza and SARS-CoV-2.
The researchers postulate that households with documented and probable respiratory pathogen transmission will have higher rates of in-home air surveillance detection. Students with more severe illnesses will be absent more often and spend more time at home, potentially leading to absenteeism being associated with greater air surveillance detections and intrahousehold transmission.
| Arm | Type | Interventions | Description |
|---|---|---|---|
| Students with ARI (acute respiratoy infection) | Experimental | Diagnostic Test: Nasal swab; Device: Indoor air quality monitor | Students with ARI and their household members will provide nasal swabs |
Sex: All, ages: 4 Years to any
Inclusion Criteria - Students: * Student attends, or is eligible to attend, a school within the Oregon School District (OSD) * Study has an illness characterized by at least 2 of 6 acute respiratory infection (ARI)/ILI symptoms (nasal discharge, nasal congestion, sneezing, sore throat, cough, fever) and student scores at least 2 points on the Jackson scale Exclusion Criteria - Students: * Household member listed on Wisconsin Department of Corrections Sex Offender Registry * Illness onset more than 7 days before anticipated time of specimen collection * Anatomical defect for which nasal specimen collection is contraindicated * Student participated too recently (<7 days from day 14 during peak influenza / COVID-19 period and <30 days during other times, as determined by a medically-attended surveillance program) Inclusion Criteria - Household member: * Live in the same household as eligible student participant * Any age and gender * Fluent in English * Able to provide appropriate consent or assent
| Facility | City | Country | Status |
|---|---|---|---|
| University of Wisconsin-Madison | Madison, Wisconsin | United States |