- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05843370
Modification of Ambient Air Pollution Exposure and Cardiopulmonary Outcomes by Socioeconomic Status and Nutrition (SENSE)
The goal of this observational study is to compare the effects of air pollution exposure and nutrition between neighborhoods with high and low social vulnerability scores. The main questions this study aims to answer are:
- Does living in a neighborhood with high or low vulnerability influence the response of the heart, lungs, and immune system to air pollution.
- Does nutritional status alter the association between air pollution exposure and changes in the heart, lungs, and immune system.
Participants (age 25-70 years) that live in neighborhoods ranked high or low on the Social Vulnerability Index (SVI) will take part in 3 visits. Each visit involves the following:
- Measurements of heart activity, lung function, and blood to measure changes that may be caused by air pollution.
- Questionnaires about the types of food eaten and activities that may modify exposure to air pollution.
- Estimation of air pollution exposure using a study iPhone. Participants will carry a study iPhone with them for 24 hours at each visit. The study iPhone runs an application (app) that estimates the amount of air pollution each participant is exposed to.
- Wearing silicone wristbands for a week before each study visit. Silicone wristbands absorb air pollutants and are later measured see the types and amounts of chemicals participants are exposed to.
Study Overview
Status
Conditions
Detailed Description
Acute and chronic exposure to air pollution are well-established risk factors for all-cause mortality, mainly driven by cardiovascular and respiratory disease. The health effects of air pollution exposure have been shown to be mediated by a range of community level and personal factors, including the presence of preexisting medical conditions, age, and socioeconomic status (SES). Individuals who reside in lower SES communities are more likely to experience increased air pollution. The effects of air pollution among those residing in less advantaged communities may be further compounded by reduced access to health care and access to nutrition. Research conducted in our facility and others has established that increased levels of micronutrients can improve subclinical indices of cardiopulmonary disease after acute and chronic air pollution. Omega-3 polyunsaturated fatty acids (PUFAs) have been demonstrated to reduce the markers of cardiopulmonary dysfunction, including heart rate variability, cholesterol, and vascular injury markers after air pollution exposure. However, levels of PUFAs, as well as other potentially protective vitamins, have been demonstrated to be significantly reduced among individuals with lower income and lower educational attainment. This may be in part due to reduced access to healthy food options, as lower income and lower educational attainment have been shown to influence access to grocery stores and nutritious foods.
Given the interplay between nutrition, air pollution exposure, SES, and cardiopulmonary disease, the investigators propose the following study to investigate how socioeconomic status can modify ambient air pollution exposure and subclinical indices of cardiovascular and pulmonary disease and inflammation, and if nutritional status can further modify this relationship. Healthy 25-70-year- old male and female subjects will be recruited from communities that are representative of high and low social vulnerability index, a composite measure of urbanicity, educational attainment, owner-occupied housing, poverty, unemployment, non-managerial occupations, single parent households, houses built since 2000, vehicle ownership, and percentage of people who pay <30% of their income on housing status. Participants will be recruited in the Raleigh-Durham-Cary combined statistical area (CSA) area of North Carolina. Qualified subjects will complete a dietary questionnaire and come to the EPA Human Studies Facility for 3 sessions. The following endpoints will be taken from subjects: blood pressure, heart rate variability (HRV), venous blood, retinal imaging, and spirometry. Blood collected will be assessed for markers of inflammation, oxidative stress, vasoconstriction, coagulation, as well as nutritional status. Air pollution exposure will be assessed for the 24-hour and weeklong period of each visit using area-specific air quality data, provided by stationary air monitors. In addition, participants will be provided with silicone wrist bands to wear for three weeklong intervals during the duration of their study. Silicone wrist bands have been shown to sorb a wide range of volatile and semi-volatile compounds and will serve as a passive personal exposure monitor to air. The investigators hypothesize that residence in a neighborhood with high social vulnerability will increase both personal exposure to air pollution and the associated health effects of air pollution exposure. The investigators further hypothesize that nutrition, specifically components in nutrition demonstrated to be anti-inflammatory, will modulate this relationship and reduce cardiopulmonary outcomes associated with exposure.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
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North Carolina
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Chapel Hill, North Carolina, United States, 27514
- EPA Human Studies Facility
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Aged 25-70 years old males and females.
- Residing in Zip Code Tabulation Area in Raleigh-Durham great triangle area representing high or low social vulnerability index (SVI).
- Continuous residence at the same address during previous one year.
Exclusion Criteria:
- Individuals with a diagnosis of COVID-19 and have persistent symptoms due to that infection (e.g., shortness of breath) or symptoms consistent with "long COVID".
- Individuals not "up to date" on their vaccinations for COVID-19. [which means a person who has received all recommended COVID-19 vaccines, including any booster dose(s) when eligible].
- Individuals who have difficulty to come to the HSF medical station on a weekday for data collection without assistance.
- Individuals have a history of heart arrhythmia, a pacemaker user, been diagnosed with arrhythmia and prescribed a medication to treat arrhythmia.
- Individuals have uncontrolled hypertension (>180 systolic, >110 diastolic)
- Individuals who are currently smoking (including vaping, hookah, e-cigarettes, including marijuana, CBD, and/or THC products) or have a smoking history within 1 year of study (defined as more than 1 pk/yr in the past year) or have a greater than/equal to a 5-pack year smoking history.
- Individuals living with a smoker who smokes inside the house.
- Individuals who are regularly exposed to high levels of vapors, dust, gases, smoke, or fumes.
- Individuals who do not understand or speak English.
- Individuals who are taking β-blocker medications.
- Individuals who are on specific extreme diets, such as liquid diet, weight loss diet, or single diet.
- Individuals who are unwilling or unable to maintain their current dietary and medication pattern for the whole study.
- Individuals with bleeding or clotting disorders.
- Individuals who have skin allergy to tape or electrodes.
- Individuals who are pregnant or attempting to become pregnant.
- Individuals currently on dialysis
- Individuals who have unspecified illnesses, which in the judgment of the investigators might increase the risk associated with clinical procedures will be a basis for exclusion.
Temporary Exclusion Criteria :
- Individuals who have had recent (within 6 months) abdominal and/or eye surgery, or been diagnosed with any type of hernia, as well as any other contraindications for raised intra-abdominal pressure.
- Individuals who have prolonged chest pain at rest (severe uncompensated angina pectoris) or inability to carry out any physical activity without chest discomfort.
- Individuals who have difficulty breathing when at rest or performing activities at daily living.
- Individuals who are having an acute respiratory illness within two weeks prior to any of the study visits.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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High SVI
Participants reside in neighborhood zip code clusters that rank at the top of the social vulnerability index (most vulnerable)
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Low SVI
Participants reside in neighborhood zip code clusters that rank at the bottom of the social vulnerability index (least vulnerable)
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Heart Rate Variability - SDNN
Time Frame: Through study completion, an average of 1-2 years
|
Time-domain measurement: standard deviation of the normal-to-normal (SDNN) in milliseconds This outcome is measured repeatedly to assess change in HRV associated with change in ambient air pollution exposure |
Through study completion, an average of 1-2 years
|
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Heart Rate Variability - rMSSD
Time Frame: Through study completion, an average of 1-2 years
|
Time-domain measurement: root-mean squared of successive differences (rMSSD) in milliseconds This outcome is measured repeatedly to assess change in HRV associated with change in ambient air pollution exposure |
Through study completion, an average of 1-2 years
|
|
Heart Rate Variability - LF absolute power
Time Frame: Through study completion, an average of 1-2 years
|
Frequency-domain measurement: Low frequency power (LF, 0.04-0.15 Hz) in ms squared divided by cycles per second (ms2/Hz). This outcome is measured repeatedly to assess change in HRV associated with change in ambient air pollution exposure |
Through study completion, an average of 1-2 years
|
|
Heart Rate Variability - VLF absolute power
Time Frame: Through study completion, an average of 1-2 years
|
Frequency-domain measurement: Very Low frequency power (VLF, 0.0033-0.04 Hz) in ms squared divided by cycles per second (ms2/Hz). This outcome is measured repeatedly to assess change in HRV associated with change in ambient air pollution exposure |
Through study completion, an average of 1-2 years
|
|
Heart Rate Variability - HF absolute power
Time Frame: Through study completion, an average of 1-2 years
|
Frequency-domain measurement: High frequency power (HF, 0.15-0.40 Hz) in ms squared divided by cycles per second (ms2/Hz). This outcome is measured repeatedly to assess change in HRV associated with change in ambient air pollution exposure |
Through study completion, an average of 1-2 years
|
|
Heart Rate Variability - LF/HF power
Time Frame: Through study completion, an average of 1-2 years
|
Frequency-domain measurement: ratio of LF power divided by HF power, expressed as ratio This outcome is measured repeatedly to assess change in HRV associated with change in ambient air pollution exposure |
Through study completion, an average of 1-2 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Pulmonary Function - FVC
Time Frame: Through study completion, an average of 1-2 years
|
Forced vital capacity (FVC) measured in Liters (L) measured via Sensor Medic Vmax pulmonary function system (dry rolling seal spirometer). This outcome is measured repeatedly to assess change in lung function associated with change in ambient air pollution exposure |
Through study completion, an average of 1-2 years
|
|
Pulmonary Function - FEV1
Time Frame: Through study completion, an average of 1-2 years
|
Forced Expiratory Volume in 1 second (FEV1) measured in Liters (L) measured via Sensor Medic Vmax pulmonary function system (dry rolling seal spirometer). This outcome is measured repeatedly to assess change in lung function associated with change in ambient air pollution exposure |
Through study completion, an average of 1-2 years
|
|
Pulmonary Function - FEV1/FVC
Time Frame: Through study completion, an average of 1-2 years
|
the ratio of Forced Expiratory Volume in 1 second (FEV1) measured in Liters (L) divided by Forced Vital Capacity (FVC) measured in Liters (L) measured via Sensor Medic Vmax pulmonary function system (dry rolling seal spirometer). Expressed as a percentage This outcome is measured repeatedly to assess change in lung function associated with change in ambient air pollution exposure |
Through study completion, an average of 1-2 years
|
|
Peripheral Venous Blood - Total Cholesterol
Time Frame: Through study completion, an average of 1-2 years
|
Total cholesterol measured in plasma in milligrams per deciliter (mg/dL) This outcome is measured repeatedly to assess change in blood lipids associated with change in ambient air pollution exposure |
Through study completion, an average of 1-2 years
|
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Peripheral Venous Blood - HDL
Time Frame: Through study completion, an average of 1-2 years
|
High density lipoproteins measured in plasma in milligrams per deciliter (mg/dL) This outcome is measured repeatedly to assess change in blood lipids associated with change in ambient air pollution exposure |
Through study completion, an average of 1-2 years
|
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Peripheral Venous Blood - LDL
Time Frame: Through study completion, an average of 1-2 years
|
Low density lipoproteins measured in plasma in milligrams per deciliter (mg/dL) This outcome is measured repeatedly to assess change in blood lipids associated with change in ambient air pollution exposure |
Through study completion, an average of 1-2 years
|
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Peripheral Venous Blood - VLDL
Time Frame: Through study completion, an average of 1-2 years
|
Very Low density lipoproteins measured in plasma in milligrams per deciliter (mg/dL) This outcome is measured repeatedly to assess change in blood lipids associated with change in ambient air pollution exposure |
Through study completion, an average of 1-2 years
|
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Peripheral Venous Blood - Triglycerides
Time Frame: Through study completion, an average of 1-2 years
|
Triglycerides measured in plasma in milligrams per deciliter (mg/dL) This outcome is measured repeatedly to assess change in blood lipids associated with change in ambient air pollution exposure |
Through study completion, an average of 1-2 years
|
|
Peripheral Venous Blood - CRP
Time Frame: Through study completion, an average of 1-2 years
|
C Reactive Protein measured in plasma in milligrams per deciliter (mg/dL) This outcome is measured repeatedly to assess change in inflammatory markers associated with change in ambient air pollution exposure |
Through study completion, an average of 1-2 years
|
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Peripheral Venous Blood - IL1B
Time Frame: Through study completion, an average of 1-2 years
|
Cytokine IL1B measured in plasma in picograms per milliliter (pg/mL) This outcome is measured repeatedly to assess change in inflammatory markers associated with change in ambient air pollution exposure |
Through study completion, an average of 1-2 years
|
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Peripheral Venous Blood - IL6
Time Frame: Through study completion, an average of 1-2 years
|
Cytokine IL6 measured in plasma in picograms per milliliter (pg/mL) This outcome is measured repeatedly to assess change in inflammatory markers associated with change in ambient air pollution exposure |
Through study completion, an average of 1-2 years
|
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Peripheral Venous Blood - IL8
Time Frame: Through study completion, an average of 1-2 years
|
Cytokine IL8 measured in plasma in picograms per milliliter (pg/mL) This outcome is measured repeatedly to assess change in inflammatory markers associated with change in ambient air pollution exposure |
Through study completion, an average of 1-2 years
|
|
Peripheral Venous Blood - TNFa
Time Frame: Through study completion, an average of 1-2 years
|
Cytokine TNFa measured in plasma in picograms per milliliter (pg/mL) This outcome is measured repeatedly to assess change in inflammatory markers associated with change in ambient air pollution exposure |
Through study completion, an average of 1-2 years
|
|
Retinal Vasculature - CRAE
Time Frame: Through study completion, an average of 1-2 years
|
Retinal images taken via non-mydriatic fundus camera are analyzed for central retinal artery equivalent (CRAE) measured in micrometer (um) This outcome is measured repeatedly to assess change in retinal vasculature associated with change in ambient air pollution exposure |
Through study completion, an average of 1-2 years
|
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Retinal Vasculature - CRVE
Time Frame: Through study completion, an average of 1-2 years
|
Retinal images taken via non-mydriatic fundus camera are analyzed for central retinal venous equivalent (CRAE) measured in micrometer (um) This outcome is measured repeatedly to assess change in retinal vasculature associated with change in ambient air pollution exposure |
Through study completion, an average of 1-2 years
|
|
Retinal Vasculature - AVR
Time Frame: Through study completion, an average of 1-2 years
|
Retinal images taken via non-mydriatic fundus camera are analyzed for arteriole to venule ratio (AVR), which is central retinal venous equivalent (CRAE) measured in micrometer (um) divided by central retinal artery equivalent (CRAE).
Expressed as a ratio T wave complexity
|
Through study completion, an average of 1-2 years
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Concentration of Air Toxics via Silicone Wrist Band
Time Frame: Through study completion, an average of 1-2 years
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Measurement of SVOCs sorbed to silicone wrist bands
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Through study completion, an average of 1-2 years
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 23-0428
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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