- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05685381
Indoor Air Quality for Black Adults With Uncontrolled Asthma
January 24, 2025 updated by: Maureen George, Columbia University
Contextualizing Asthma Self-Management With Measures of Indoor Air Quality for Black Adults With Uncontrolled Asthma
The aims of this project are twofold:
- to characterize indoor air quality components obtained from apartments with gas stoves and open kitchens in a cohort of Black adults with uncontrolled asthma recruited from federally qualified health centers and enrolled in the parent study.
- to conduct a comprehensive assessment of feasibility, implementation, and acceptability of the study.
Study Overview
Status
Completed
Conditions
Detailed Description
People spend as much as 90% of their time indoors, making indoor air quality (IAQ) particularly important to health.
Many homes in New York City, particularly low-income housing, contain gas kitchen appliances, which generate fuel through the combustion of natural gas, generating indoor pollutants.
Increasing evidence finds that even low levels of these pollutants are hazardous for human health.
Those most vulnerable to ambient air pollution live in homes with gas appliances and inadequate ventilation.
Moreover, individuals with pre-existing diseases like asthma are particularly susceptible to adverse health effects from poor IAQ, which gas stoves may exacerbate.
This study addresses the important problem of uncontrolled asthma among a group at high risk for asthma and its adverse effects - Black adults who reside in homes with gas stoves and open kitchens.
The investigator aims to characterize indoor air quality components in a cohort enrolled in the parent R01 (NCT05341726) and conduct a comprehensive assessment of feasibility including process, implementation and acceptability metrics.
Identifying new targets for asthma self-management that could produce better health outcomes, thus addressing an important health inequity issue.
Study Type
Observational
Enrollment (Actual)
30
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
New York
-
Beacon, New York, United States, 12508
- Sun River Health
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Brooklyn, New York, United States, 11216
- Bedford Stuyvesant Family Health Center
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Black adults with persistent asthma that receive care at partner federally qualified health centers
Description
Inclusion Criteria (participants):
Patient participants will
- be adults (> or = 18 years of age)
- self-report race as 'Black' race (African American, African, Caribbean, West Indian, multi-racial [Black AND one or more additional races]); identify their ethnicity as Hispanic OR non-Hispanic
- have clinician-diagnosed persistent asthma (defined as being prescribed inhaled corticosteroids in the last 48 months) or have had an asthma exacerbation (e.g., ER visit, course of Prednisone) regardless of controller medicine use
- receive asthma care at a partner federally qualified health center and
- screen positive for uncontrolled asthma as measured by the Asthma Control Questionnaire- 6 items (ACQ-6) and erroneous beliefs as measured by the Conventional and Alternative Management for Asthma (CAM-A) survey.
Exclusion Criteria (participants):
- non-English speaking or
- serious mental health conditions that preclude completion of study procedures or confound analyses
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
- Observational Models: Case-Control
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
|---|
|
Black adults with persistent asthma in homes with gas kitchen appliances
Black adults with persistent asthma that reside in homes with kitchen appliances (i.e., cooktops, ovens, and ranges) fueled by combustible gas.
|
|
Black adults with persistent asthma in homes without gas kitchen appliances
Black adults with persistent asthma that reside in homes with kitchen appliances (i.e., cooktops, ovens, and ranges) not fueled by combustible gas.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Completion of acceptability questionnaire
Time Frame: Post-trial visit (up to 3 months after intervention completion)
|
The number of participants who complete the acceptability questionnaire.
The acceptability questionnaire is a semi-structured interview at the time of indoor air quality sample retrieval and will be guided by the constructs of the Theoretical Framework of Acceptability (e.g., burden, user experience, attitudes, participation intentions).
|
Post-trial visit (up to 3 months after intervention completion)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Maureen George, PhD, Columbia University School of Nursing
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)
January 19, 2023
Primary Completion (Actual)
December 31, 2023
Study Completion (Actual)
February 14, 2024
Study Registration Dates
First Submitted
January 5, 2023
First Submitted That Met QC Criteria
January 5, 2023
First Posted (Actual)
January 17, 2023
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
January 24, 2025
Last Verified
January 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- AAAT0939 - sub-study
- 3R01NR019275-02S1 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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