Developing and Evaluating an Indoor Air Pollution Intervention Among Cardiovascular Patients: the AIRWISE Study
NCT ID: NCT06384625
Last Updated: 2025-11-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
20 participants
INTERVENTIONAL
2024-07-24
2025-11-05
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
OTHER
NONE
Study Groups
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Air pollution intervention implementation
AIRWISE intervention implementation
AIRWISE
AIRWISE (Air Improvement and Real-time Monitoring for Wellness through Interactive Strategies and Education) utilizes personal air cleaners (PACs) to filter indoor air, while enhanced aspects focus on improving compliance to PAC use. Key components include low-cost sensors (PurpleAir, Inc, USA) that change color according to air quality index (AQI) and behavioral recommendations that correspond to varying AQI levels.
Interventions
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AIRWISE
AIRWISE (Air Improvement and Real-time Monitoring for Wellness through Interactive Strategies and Education) utilizes personal air cleaners (PACs) to filter indoor air, while enhanced aspects focus on improving compliance to PAC use. Key components include low-cost sensors (PurpleAir, Inc, USA) that change color according to air quality index (AQI) and behavioral recommendations that correspond to varying AQI levels.
Eligibility Criteria
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Inclusion Criteria
* One primary residence (5+ days per week)
* Own a computer or electronic device (tablet or phone with web browser), and reliable internet connection or cell phone service (required to submit study surveys)
* Access to a working email address (required to submit study surveys)
* Electricity in the home (required to power the study equipment)
Exclusion Criteria
* Current use of stand-alone home high efficiency purified air (HEPA) filtration or PAC unit in the home
* Intention to move in the next 6 months
* Another person in the household is enrolled in this study (one person per household can enroll)
* Having any health condition that prevents the participants from having blood pressure measured using an upper-arm cuff: lymphedema, paresis or paralysis, arterial or venous lines/catheters, dialysis shunt, recent surgical wounds, or mastectomy
55 Years
ALL
No
Sponsors
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Providence Heart Institute
UNKNOWN
University of Montana
OTHER
Responsible Party
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Locations
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University of Montana
Missoula, Montana, United States
Countries
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Other Identifiers
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361378
Identifier Type: -
Identifier Source: org_study_id