A Study Evaluating the Use of an Indoor Air Quality Monitor to Promote a Smoke-free Home

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMemorial Sloan Kettering Cancer Center

About this trial

The purpose of this study is to evaluate how using an indoor air quality monitor can promote a smoke-free home for cancer patients who are enrolled in MSK's Tobacco Treatment Program.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Adult (aged >18 years) MSK patients as per the EHR

Has been referred and enrolled in the MSK TTP and completed the initial counseling session as per the TTP clinical database

Reports current (within the past 30 days) tobacco use (i.e., cigarettes and/or any other tobacco products) as per the TTP Intake form

Must be English-speaking in the EHR

Disqualifiers

Patient reports that no smoking is allowed, by them or anyone else, in the home as per the TTP intake form and/or per self-report

Trial design

Design model

Single group

Treatments tested in this trial

  • Indoor Air Quality Monitor AirGradient ONE

    Other intervention

    Participants will be asked to set up an Indoor Air Quality Monitor AirGradient ONE (Model: I-9PSL) which is an award winning commercially available indoor air quality monitor designed to enable anyone to monitor their air quality in their home for about 60 days (8 weeks). Indoor air pollution levels within participating households will be measured using these AQMs.

Treatment groups

10 Participants
are divided into 1 treatment group
Group A: MSK Participants who are current smokersExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Percentage of participants using the air quality monitoring device for 14 consecutive days

Assess the feasibility and acceptability of collecting environmental data on biomarkers of household air quality (AQ) and smoke exposure using low-cost, AQMs as an intermediate endpoint of a smoke-free-home.

Time frame
up to 8 weeks
2

Percentage of participants who attend the study-specific smoke-free workshop sessions

Assess the feasibility and acceptability of tobacco treatment adherence among individuals diagnosed with cancer.

Time frame
Up to 8 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.