Actively Recruiting

Phase Not Applicable
Age: 6Years - 90Years
All Genders
Healthy Volunteers
ID05953233

School Inner City Air Study to Evaluate Active and Sham HEPA Cleaners in Elementary Classrooms

Led by Massachusetts General Hospital · Updated on 2025-12-11

200

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

Sponsors

M

Massachusetts General Hospital

Lead Sponsor

B

Boston Children's Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the use of high efficiency particulate air (HEPA) cleaners in elementary school classrooms to see if they can reduce exposure to respiratory viruses and infections among students, teachers, and their family members. This randomized clinical trial aims to answer whether active classroom HEPA cleaners can lower virus presence and symptomatic infections compared to sham (inactive) HEPA cleaners. Classrooms will be randomly assigned to have either active HEPA cleaners or sham devices placed throughout the school year. The active cleaners are commercially available portable HEPA units, while the sham cleaners are similar devices with their filtration components removed. Both types will be used continuously during the school year in the study classrooms. Participants include students, teachers, and household members from the enrolled classrooms. Researchers will collect air samples from classrooms over time, nasal samples from participants, and symptom surveys using the Wisconsin Upper Respiratory Symptom Survey. Viral testing will be done with digital polymerase chain reaction (dPCR) to detect viral pathogens. The main outcome measured is viral presence in upper respiratory samples after one year, along with secondary outcomes such as symptomatic infections and severity, missed school or work days, and healthcare visits. The study involves monitoring for one full year.

CONDITIONS

Brief Title

School Inner City Air Study

Who Can Participate

Age: 6Years - 90Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Children in grades K-5 (ages 6 to 12 years)
  • Attend a participating school where environmental samples can be collected
  • No plans to change schools within the next 12 months
  • Ability to understand and provide informed consent (child or parent/guardian)
  • Adults aged 21 or older who are parents, caretakers, household members of participating children, or teachers in participating classrooms
  • Adults able to understand and provide informed consent
Not Eligible

You will not qualify if you...

  • Children unable or contraindicated to perform home self-collection of nasal swabs
  • Children with severe chronic diseases affecting mobility (e.g., cancer, genetic or congenital disorders)
  • Children with severe neurobehavioral, neurodevelopmental, or psychiatric disorders requiring special assistance
  • Families not fluent enough in English or Spanish to complete study surveys
  • Adults unable or contraindicated to perform home self-collection of nasal swabs
  • Adults with severe chronic diseases affecting mobility (e.g., cancer, genetic or congenital disorders)
  • Adults with severe neurobehavioral, neurodevelopmental, or psychiatric disorders requiring special assistance
  • Families not fluent enough in English or Spanish to complete study surveys

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - Up to 1 year

Active or sham HEPA cleaners are placed in classrooms throughout the school year.

Classroom air samples and respiratory samples collected longitudinally; symptom surveys completed regularly

Long-term Monitoring

Duration - Up to 1 year

Participants are observed for respiratory health outcomes and viral pathogen presence during the study period.

Ongoing symptom surveys and sample collections throughout the study

Trial Site Locations

Total: 1 location

1

Mass General Brigham

Boston, Massachusetts, United States, 02114

Actively Recruiting

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Research Team

P

Peggy Lai, MD MPH

W

Wanda Phipatanakul, MD MS

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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