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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05953233
Other study ID # IRB-P00045373
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 2023
Est. completion date August 2030

Study information

Verified date August 2023
Source Massachusetts General Hospital
Contact Peggy Lai, MD MPH
Phone 617-875-9878
Email plai@mgh.harvard.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this randomized clinical trial is to test the efficacy of high efficiency particulate air (HEPA) cleaners in reducing respiratory viral exposure and infections in elementary school classrooms. Classrooms will be randomized to active vs. sham HEPA cleaners. The main questions it aims to answer are: - Do classroom HEPA cleaners reduce exposure to viruses? - Do classroom HEPA cleaners reduce student and teacher infections? - Do classroom HEPA cleaners reduce infections in family members?


Description:

Classrooms from participating schools will be randomized to active vs. sham HEPA cleaners. From enrolled classrooms, we will enroll students, teachers, and members of the household. We will collect the following: - longitudinal classroom air samples - longitudinal upper respiratory samples - longitudinal symptom surveys using the Wisconsin Upper Respiratory Symptom Survey (WURSS) Viral testing on collected air and respiratory samples will be performed using digital polymerase chain reaction (dPCR).


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 200
Est. completion date August 2030
Est. primary completion date August 2029
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 6 Years to 90 Years
Eligibility Inclusion Criteria: Children - Grades K-5 (age 6-12 years) - Attend one of the schools that the study team has permission to obtain classroom/school environmental samples - Have no plans to move schools within the upcoming 12 months - Subject and/or parent guardian must be able to understand and provide informed consent and also willing to participate in the study Adults - Adult (age 21 or older) parent, caretaker, or household member of child participating in this study, or teacher in classroom participating in study - Able to understand and provide informed consent Exclusion Criteria: Children - Contraindication to or inability to participate in home self-collection of nasal swab samples - Severe chronic diseases (e.g. cancer, genetic or congenital disorders interfering with mobility) - Severe neurobehavioral, neurodevelopmental or psychiatric disorders requiring special assistance - Families who do not speak English or Spanish well enough to complete the survey questions, as validated versions in other languages are not available for all of the measures Adults - Contraindication to or inability to participate in home self-collection of nasal swab samples - Severe chronic diseases (e.g. cancer, genetic or congenital disorders interfering with mobility) - Severe neurobehavioral, neurodevelopmental or psychiatric disorders requiring special assistance - Families who do not speak English or Spanish well enough to complete the survey questions, as validated versions in other languages are not available for all of the measures

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Active classroom HEPA cleaner
Commercially available portable HEPA cleaner
Sham classroom HEPA cleaner
Commercially available portable HEPA cleaner with filtration device removed

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Massachusetts General Hospital Boston Children's Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Viral pathogen detected in upper respiratory sample Presence/absence of a respiratory virus in upper respiratory sample 1 year
Secondary Symptomatic respiratory infection (student, teacher) Presence/absence of a cold based on 30 day recall 1 year
Secondary Symptomatic respiratory infection (household member) Presence/absence of a cold based on 30 day recall 1 year
Secondary Viral detection in classroom bioaerosol sample Viral detection in classroom bioaerosol sample (viral copy number per cubic meter of air) 1 year
Secondary Severity of a cold in child using the WURSS-K - Kids Daily Symptom Report Severity of a cold (when present) in child will be graded using the Wisconsin Upper Respiratory Symptom Survey Kids Daily Symptom Report (WURSS-K). Range 0 - 42; higher indicates more severe. 1 year
Secondary Severity of a cold in adult using the WURSS-24 Severity of a cold (when present) in adult will be graded using the Wisconsin Upper Respiratory Symptom Survey 24 Daily Symptom Report (WURSS-24). Range 0 - 161; higher indicates more severe. 1 year
Secondary Number of missed school or work days in last 30 days 30 day recall of missed school or work days. Range 0 - 30; higher indicates more severe. 1 year
Secondary Number of days requiring inpatient or outpatient care in last 30 days 30 day recall of healthcare utilization defined as number of days requiring outpatient or inpatient hospital care. Range 0 - 30; higher indicates more severe. 1 year
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