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Effect of Commute Traffic on Vascular Function

Effect of Commute Traffic on Vascular Function

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05454930
Enrollment
16
Registered
2022-07-12
Start date
2015-01-31
Completion date
2016-12-31
Last updated
2022-07-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Diseases

Keywords

air pollution, traffic, vascular function, gasoline exhaust, diesel exhaust

Brief summary

The investigators will assess the vascular effects of riding in a car in heavily trafficked roadways, and whether filtering the car's air reduces those effects.

Detailed description

In this double-blind, crossover trial, randomized to order, recruited participants will be screened and then will accompany the study team on three typical commutes on separate days with sufficient washout (i.e., three weeks) between drives. One day this will occur with an effective filter system in the vehicle and the other two days without effective filtration; ineffective filtration is the most typical actual vehicle condition. Subjects will be unaware of the filtration conditions of the commute on that day. Each subject's experimental sessions will occur at the same time of day and will be separated by at least 21 days. The two sessions (either filtered air or traffic-derived entrained air) will be 120 minutes in duration and will encompass routes on heavily traveled roadways in the Seattle area. Before subjects begin the commute trials, they will go through the consent process and a series of screening tests. The study investigators will assess a series of measures regarding vascular function before and after each drive.

Interventions

The vehicle is fitted with a (High-Efficiency Particulate Absorbing, HEPA) filter device incorporating a charcoal filter, as well as an augmented cabin filter

Sponsors

Environmental Protection Agency (EPA)
CollaboratorFED
National Institute of Environmental Health Sciences (NIEHS)
CollaboratorNIH
University of Washington
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 49 Years
Healthy volunteers
Yes

Inclusion criteria

* healthy

Exclusion criteria

* asthma, * high blood pressure, * diabetes, * high cholesterol, * other chronic conditions requiring ongoing medical care.

Design outcomes

Primary

MeasureTime frameDescription
Gene Expression and DNA methylation30 minutes before 120 minute driving session; 30 minutes, 5 hour, and 24 hours post-driving sessionanalysis in circulating mononuclear cells; determined via fold change in abundance
Change in Brachial Artery Diameter from Pre-Drive to Post-Drive30 minutes before 120 minute driving session; 30 minutes post driving sessionUltrasound assessment of brachial artery diameter, in millimeters.
Change in Blood Pressure from Pre-Drive to During-Drive and Post-drive10 minutes before driving session; 15, 30, 45, 60, 75, 90, 100, 120 minutes following start of (120 minute) driving session; 10 minutes, 1.5 hours, 3.5 hours, 6 hours, 24 hours after end of driving session.systolic and diastolic blood pressure measured in mmHg
Change in Retinal Arteriolar Diameter from Pre-Drive to Post-Drive30 minutes before 120 minute driving session; 30 minutes post driving sessionmeasured by retinal photography, image analysis, in micrometers

Secondary

MeasureTime frameDescription
circulating stress hormone30 minutes before 120 minute driving session; 5 hour and 24 hours post-driving sessioncortisol by chemiluminescence (ng/mL)
complete blood count with differential30 minutes before 120 minute driving session; 5 hour and 24 hours post-driving sessionlaboratory values for hematologic indices (cells/uL)
inflammatory marker interleukin-630 minutes before 120 minute driving session; 5 hour and 24 hours post-driving sessioninterleukin-6 determined by chemiluminescence (pg/mL)
inflammatory marker c-reactive protein30 minutes before 120 minute driving session; 5 hour and 24 hours post-driving sessionC-reactive protein by immunoturbidimetry (ug/mL)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026