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Effect of Commute Traffic on Vascular Function

8. juli 2022 opdateret af: Joel Daniel Kaufman, University of Washington
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.

Studieoversigt

Status

Afsluttet

Betingelser

Intervention / Behandling

Detaljeret beskrivelse

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.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

16

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

    • Washington
      • Seattle, Washington, Forenede Stater, 98195
        • University of Washington Medical Center

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år til 49 år (Voksen)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • healthy

Exclusion Criteria:

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

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Forebyggelse
  • Tildeling: Randomiseret
  • Interventionel model: Crossover opgave
  • Maskning: Firedobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Ingen indgriben: Typical Commute
Participants spend two hours in automobile, on heavily trafficked roadways, without active filtration of air pollutants
Andet: Typical Commute, Filtered Air
Participants spend two hours in automobile, on heavily trafficked roadways, with active filtration of air pollutants
The vehicle is fitted with a (High-Efficiency Particulate Absorbing, HEPA) filter device incorporating a charcoal filter, as well as an augmented cabin filter

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change in Brachial Artery Diameter from Pre-Drive to Post-Drive
Tidsramme: 30 minutes before 120 minute driving session; 30 minutes post driving session
Ultrasound assessment of brachial artery diameter, in millimeters.
30 minutes before 120 minute driving session; 30 minutes post driving session
Change in Blood Pressure from Pre-Drive to During-Drive and Post-drive
Tidsramme: 10 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
10 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.
Change in Retinal Arteriolar Diameter from Pre-Drive to Post-Drive
Tidsramme: 30 minutes before 120 minute driving session; 30 minutes post driving session
measured by retinal photography, image analysis, in micrometers
30 minutes before 120 minute driving session; 30 minutes post driving session
Gene Expression and DNA methylation
Tidsramme: 30 minutes before 120 minute driving session; 30 minutes, 5 hour, and 24 hours post-driving session
analysis in circulating mononuclear cells; determined via fold change in abundance
30 minutes before 120 minute driving session; 30 minutes, 5 hour, and 24 hours post-driving session

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
circulating stress hormone
Tidsramme: 30 minutes before 120 minute driving session; 5 hour and 24 hours post-driving session
cortisol by chemiluminescence (ng/mL)
30 minutes before 120 minute driving session; 5 hour and 24 hours post-driving session
complete blood count with differential
Tidsramme: 30 minutes before 120 minute driving session; 5 hour and 24 hours post-driving session
laboratory values for hematologic indices (cells/uL)
30 minutes before 120 minute driving session; 5 hour and 24 hours post-driving session
inflammatory marker interleukin-6
Tidsramme: 30 minutes before 120 minute driving session; 5 hour and 24 hours post-driving session
interleukin-6 determined by chemiluminescence (pg/mL)
30 minutes before 120 minute driving session; 5 hour and 24 hours post-driving session
inflammatory marker c-reactive protein
Tidsramme: 30 minutes before 120 minute driving session; 5 hour and 24 hours post-driving session
C-reactive protein by immunoturbidimetry (ug/mL)
30 minutes before 120 minute driving session; 5 hour and 24 hours post-driving session

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: Joel Kaufman, MD, University of Washington

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. januar 2015

Primær færdiggørelse (Faktiske)

1. juli 2016

Studieafslutning (Faktiske)

1. december 2016

Datoer for studieregistrering

Først indsendt

31. juli 2015

Først indsendt, der opfyldte QC-kriterier

8. juli 2022

Først opslået (Faktiske)

12. juli 2022

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

12. juli 2022

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

8. juli 2022

Sidst verificeret

1. juli 2022

Mere information

Begreber relateret til denne undersøgelse

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • STUDY00001196
  • K24ES013195 (U.S. NIH-bevilling/kontrakt)
  • RD-83479601 (Andet bevillings-/finansieringsnummer: US Environmental Protection Agency STAR)

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Kliniske forsøg med Hjerte-kar-sygdomme

Kliniske forsøg med Filtered Air

Abonner