- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06693700
A Study Evaluating the Use of an Indoor Air Quality Monitor to Promote a Smoke-free Home
October 21, 2025 updated by: Memorial Sloan Kettering Cancer Center
Freedom to Breathe: Pilot Study Towards Achieving Environmental Justice for Cancer Patients and Their Families
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.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
10
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Michael Bellamy, PhD
- Phone Number: 212-639-2045
- Email: bellamym@mskcc.org
Study Contact Backup
- Name: Gleneara Bates-Pappas, PhD, LMSW
- Phone Number: 212-610-0507
- Email: batespag@mskcc.org
Study Locations
-
-
New Jersey
-
Basking Ridge, New Jersey, United States, 07920
- Recruiting
- Memorial Sloan Kettering Basking Ridge (Consent Only)
-
Contact:
- Gleneara Bates-Pappas, PhD, LMSW
- Phone Number: 212-610-0507
-
Middletown, New Jersey, United States, 07748
- Recruiting
- Memorial Sloan Kettering Monmouth (Consent Only)
-
Contact:
- Gleneara Bates-Pappas, PhD, LMSW
- Phone Number: 212-610-0507
-
Montvale, New Jersey, United States, 07645
- Recruiting
- Memorial Sloan Kettering Bergen (Consent Only)
-
Contact:
- Gleneara Bates-Pappas, PhD, LMSW
- Phone Number: 212-610-0507
-
-
New York
-
Commack, New York, United States, 11725
- Recruiting
- Memorial Sloan Kettering Suffolk-Commack (Consent only)
-
Contact:
- Gleneara Bates-Pappas, PhD, LMSW
- Phone Number: 212-610-0507
-
Harrison, New York, United States, 10604
- Recruiting
- Memorial Sloan Kettering Westchester (Consent only)
-
Contact:
- Gleneara Bates-Pappas, PhD, LMSW
- Phone Number: 212-610-0507
-
New York, New York, United States, 10065
- Recruiting
- Memorial Sloan Kettering Cancer Center (All Protocol Activities)
-
Contact:
- Gleneara Bates-Pappas, PhD,LMSW
- Phone Number: 212-610-0507
-
New York, New York, United States, 10031
- Not yet recruiting
- City College of New York (Data Collection AND Data Analysis)
-
Contact:
- Prash Naidu, MD
- Email: pnaidu@ccny.cuny.edu
-
Uniondale, New York, United States, 11553
- Recruiting
- Memorial Sloan Kettering Nassau (Consent Only)
-
Contact:
- Gleneara Bates-Pappas, PhD, LMSW
- Phone Number: 212-610-0507
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- 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
- Must be reachable by phone as per self-report
- Must have Wi-Fi available at home as per self-report
Exclusion Criteria:
- 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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: MSK Participants who are current smokers
10 MSK participants who are current smokers and receiving tobacco treatment will be enrolled.
|
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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Percentage of participants using the air quality monitoring device for 14 consecutive days
Time Frame: up to 8 weeks
|
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.
|
up to 8 weeks
|
|
Percentage of participants who attend the study-specific smoke-free workshop sessions
Time Frame: Up to 8 weeks
|
Assess the feasibility and acceptability of tobacco treatment adherence among individuals diagnosed with cancer.
|
Up to 8 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Gleneara Bates-Pappas, PhD, LMSW, Memorial Sloan Kettering Cancer Center
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 14, 2024
Primary Completion (Estimated)
November 14, 2027
Study Completion (Estimated)
November 14, 2027
Study Registration Dates
First Submitted
November 14, 2024
First Submitted That Met QC Criteria
November 14, 2024
First Posted (Actual)
November 18, 2024
Study Record Updates
Last Update Posted (Estimated)
October 22, 2025
Last Update Submitted That Met QC Criteria
October 21, 2025
Last Verified
October 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 24-260
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
Memorial Sloan Kettering Cancer Center supports the international committee of medical journal editors (ICMJE) and the ethical obligation of responsible sharing of data from clinical trials.
The protocol summary, a statistical summary, and informed consent form will be made available on clinicaltrials.gov
when required as a condition of Federal awards, other agreements supporting the research and/or as otherwise required.
Requests for deidentified individual participant data can be made beginning 12 months after publication and for up to 36 months post publication.
Deidentified individual participant data reported in the manuscript will be shared under the terms of a Data Use Agreement and may only be used for approved proposals.
Requests may be made to: crdatashare@mskcc.org.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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