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N/A N=33 Randomized Triple-blind Prevention

Reducing Particulate Matter-associated Cardiovascular Health Effects for Seniors

Cardiometabolic Health

Enrolled (actual)
33
Serious AEs
0.0%
Results posted
Jan 2026
Primary outcome: Primary: Systolic Blood Pressure — 127.0; 126.5 mm Hg — p=0.588

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
air filtration with air purifier with hepa filter (Other); sham (Other)
Age
Adult, Older Adult · 60+ yrs
Sex
All
Sponsor
University of Michigan
Primary completion
Nov 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Systolic Blood Pressure
127.0; 126.5 0.588
SECONDARY
Diastolic Blood Pressure
75.1; 75.3 0.748
SECONDARY
Atmospheric Particulate Matter (pm2.5) - Indoor
1.3; 8.3 <0.001 sig
SECONDARY
Atmospheric Particulate Matter (pm2.5) - Outdoor
10.3; 8.9 0.0764
SECONDARY
24-hr Personal PM2.5 (Filter-gravimetric Mass)
5.1; 12.4 <0.001 sig
SECONDARY
Black Carbon, Hourly Personal PM2.5 Levels
SECONDARY
Aortic Hemodynamics
SECONDARY
Insulin Sensitivity
SECONDARY
Adrenal Steroid Panel

Summary

Exposure to fine particulate matter (PM2.5) air pollution is an established risk factor for cardiovascular (CV) morbidity.

Eligibility Criteria

Inclusion Criteria

  • Nonsmoker
  • ≥60 years old
  • residing in Carpenter Place Apartments

Exclusion Criteria

  • Active cigarette smoker
  • daily secondhand smoke exposure (self-report)
  • any CV event (myocardial infarction, stroke, heart failure, revascularization) in the past 3 months
  • unstable CV condition or risk factor (uncontrolled diabetes, class 3-4 angina or heart failure) or any medical condition that would place the participant at risk from participation or jeopardize study integrity (per investigators)
  • expected overnight travel outside their apartment during the 14-week study period
  • unable to provide informed consent
  • lung disease requiring oxygen
  • renal dialysis
  • cancer receiving active treatment or chemotherapy
  • severe uncontrolled high BP ≥160/100 mm Hg or SBP<115 mm Hg.
  • CV medication change in the prior month. If participants are on medications for high BP, diabetes, or a CV condition, they will need to have stable therapy during the prior month with no planned changes during the study period.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04103346). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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