Inflammation Clinical Trial
— DESTRESSOfficial title:
Effects of Mental Stress and Diesel Exhaust on Cardiovascular Health
This study uses an experimental design to conduct a double-blind, randomized, crossover study where participants receive both diesel exhaust and a mental stress test in a controlled setting. My hypothesis is that the synergistic effect of stress and air pollution will result in higher levels of stress and inflammation (measured via biological markers) as well as poorer cardiovascular disease related outcomes compared to the independent effect of each exposure separately.
Status | Recruiting |
Enrollment | 22 |
Est. completion date | January 2020 |
Est. primary completion date | January 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 22 Years to 49 Years |
Eligibility |
Inclusion Criteria: Non-smokers without history of high blood pressure, asthma, diabetes, high cholesterol, post-traumatic stress disorder (PTSD) or any other chronic condition that requires ongoing care. Exclusion Criteria: 1. Smoking: We rule out active smoking by checking urine cotinine during our study. 2. History of high blood pressure: We objectively measure BP during in-person screening and exclude those with blood pressure (>130/85 mmHg). 3. Asthmatic: Spirometry is done at screening to rule out asthma. 4. Diabetic: We obtain fasting blood sugar to rule out diabetes at screening (>125 mg/dL) 5. Cholesterol: We obtain fasting blood lipid levels to rule out hypercholesterolemia at screening (>200 mg/dL). 6. History of PTSD: Subjects will be asked about prior PTSD diagnosis during the phone and in person screen. 7. Any other chronic condition requiring ongoing care based on medication use. 8. A body mass index (weight in kilograms divided by height in meters squared) greater than 26 and less than 18.5 9. A female of childbearing age with a positive pregnancy test 10. A female of childbearing age who is unwilling to use effective contraception during the study |
Country | Name | City | State |
---|---|---|---|
United States | University of Washington Diesel Exhaust Facility | Seattle | Washington |
Lead Sponsor | Collaborator |
---|---|
University of Washington | National Institute of Environmental Health Sciences (NIEHS) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Change in blood pressure | blood pressure in mm Hg | Change in blood pressure from baseline (pre-exposure) to 22 hours post exposure | |
Other | Change in heart rate | heart rate in beats per minute | Change in blood pressure from baseline (pre-exposure) to 60 minutes post exposure | |
Primary | Change in norepinephrine | Urinary norepinephrine in ng/mg | Change in norepinephrine from baseline (pre-exposure) to immediately after exposure | |
Primary | Change in epinephrine | Urinary epinephrine in ng/mg | Change in epinephrine from baseline (pre-exposure) to immediately after exposure | |
Primary | Change in dopamine | Urinary dopamine in ng/mg | Change in dopamine from baseline (pre-exposure) to immediately after exposure | |
Secondary | Change in d-dimer | plasma d-dimer (ug/ml) is a measure of coagulation | change in d-dimer from baseline (pre-exposure) to six hours post exposure | |
Secondary | Change in fibrinogen | plasma fibrinogen (mg/dl) is a measure of coagulation | change in fibrinogen from baseline (pre-exposure) to six hours post exposure | |
Secondary | Change in interleukin-6 (IL-6) | plasma IL-6, measured in pg/ml, is a marker of inflammation | change in IL-6 from baseline (pre-exposure) to immediately after exposure | |
Secondary | Change in tumor necrosis factor alpha (TNF-a) | plasma TNF-a, measured in pg/ml, is a marker of inflammation | change in TNF-a from baseline (pre-exposure) to immediately after exposure | |
Secondary | Change in interleukin-1b (IL-1b) | plasma IL-1b, measured in pg/ml, is a marker of inflammation | change in IL-1b from baseline (pre-exposure) to immediately after exposure |
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