Clinical Trials Directory

Trials / Completed

CompletedNCT04770597

Monitors to Improve Indoor Carbon Dioxide (CO2) Concentrations in the Hospital

Monitors to Improve Indoor Carbon Dioxide (CO2) Concentrations in the Hospital: a Randomized, Sham-controlled, Open Label Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
12 (actual)
Sponsor
Imelda Hospital, Bonheiden · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

Ventilation with fresh outdoor air has recently gained considerable attention as a means to reduce the potential risk of indoor aerosol transmission of respiratory pathogens such as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus causing coronavirus disease 2019 (COVID-19). Commercial carbon dioxide (CO2) monitors are increasingly used in schools, long-term care facilities, offices and public buildings to monitor indoor ventilation. However, no formal evidence is available to support the effectiveness of feedback from CO2 monitoring devices. Moreover, modern hospitals have superior indoor air quality control systems. The aim of this prospective pilot randomized controlled trial (RCT) is to evaluate whether CO2 monitoring devices would be useful as a means to further maintain lower indoor CO2 concentrations in hospitals.

Detailed description

In this pilot, randomized, sham-controlled open-label RCT, hospital rooms will be fitted with Aranet4 Home CO2 sensors. Each device will continuously measure indoor CO2 concentrations at 1-minute intervals during 4 time periods: 1\. Baseline: staff blinded to CO2 levels displayed on sensor 2-3. Sham/Intervention period: sensors on the same ward will be randomized to placebo (sensor not showing CO2 levels to staff) or Intervention (sensor displaying CO2 levels to staff) in a cross-over design 4\. Post-intervention phase (3 weeks post-intervention): staff blinded to CO2 levels Each measurement period will consist of 7 days with no washout period. Our primary hypothesis is that CO2 sensors will record less time (minutes) with elevated CO2 levels during the intervention period, compared to the Sham periods. However, carry-over effects will be investigated by comparing the Intervention periods to the Baseline and Post-intervention phases. Note \[February 27, 2021\]: due to technical problems with the Aranet4 device Bluetooth connection, outcome data will be analyzed according to measurement data at 2-5 minute intervals (measurements can be made every minute, but data cannot be downloaded with the current version of the app due to technical problems).

Conditions

Interventions

TypeNameDescription
DEVICEAranet4 Home CO2 monitorThe sensor is placed in the room at a height between 1 and 2 meters and not near the window or door.

Timeline

Start date
2021-02-21
Primary completion
2021-05-02
Completion
2021-05-02
First posted
2021-02-25
Last updated
2021-05-11

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT04770597. Inclusion in this directory is not an endorsement.