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DRIIVE (Data and Research on Interventions to Improve the Vehicular Environment)

DRIIVE (Data and Research on Interventions to Improve the Vehicular Environment)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02381626
Enrollment
39
Registered
2015-03-06
Start date
2014-12-31
Completion date
2020-10-18
Last updated
2021-10-05

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

Conditions

Vehicular Environment

Keywords

HEPA filter, 14-247

Brief summary

The purpose of this study is to look at air quality in cabs and see if the air quality inside taxi cabs is connected to increased risks for lung and heart health problems. Another purpose of the study is to see if putting an air filter inside the car may help improve the air quality and lower health risks. This is important because air pollution can be harmful to health. Air pollution is made up of very tiny particles (things) floating in the air around us, called particulate matter. Particulate matter is made up of dust, smoke, dirt, and gas fumes and can get into our bodies as we breathe. It has been linked to risk for lung cancer and heart disease. It is important because taxi drivers spend many hours of their day inside their cars. The investigators hope that this study will help them find out if using air filters inside cabs will help lower the levels of pollution in cabs and reduce its effects on the health of taxi drivers. They will use these results to educate the taxi driver community.

Detailed description

DRIIVE (Data and Research on Interventions to Improve the Vehicular Environment) is a community-engaged translational pilot project that will utilize a three parallel arm design to obtain preliminary data on associations between Particulate Matter (PM)/air pollution and physiologic measurements and biomarkers in taxi drivers, and to determine the impact of a HEPA filter (to remove PM and volatile organic compounds) intervention on such physiologic measurements and biomarkers. DRIIVE is funded by the New York State Department of Health Empire Clinical Research Investigator Program (ECRIP), which trains physicians in clinical research in New York. Drivers will be randomized to one of two groups: Intervention or Wait-list Control. In total, two groups of 14 participants in each group will be recruited: 1) Wait List Control group, who will receive a HEPA filter at the end of the 1 month participation period, and 2) Intervention group, who will receive a HEPA filter two weeks into their participation period. The project will be completed within a 2 year timeframe.

Interventions

DEVICEHEPA air purifier

air purifiers to remove PM and volatile organic compounds will be placed in drivers cars

BEHAVIORALquestionnaires
OTHERLog-book

PM and biological measurements

OTHERUrine sample

PAH (Polycyclic Aromatic Hydrocarbon) will be assessed via urine sample collection of Urinary 1 hydroxy pyrene and particulate matter collected via Polyurethane Foam Filter (PUF) sampler

Sponsors

New York University
CollaboratorOTHER
New York State Department of Health
CollaboratorOTHER_GOV
The City College of New York
CollaboratorOTHER
Memorial Sloan Kettering Cancer Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
21 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

Drivers: * Full-time New York City cab drivers; * Non Smokers (assessed by modified BRFSS smoking question within screening tool) ; * Male; * Between the ages of 21 and 90; * No immediate plans (within the next 3 months) to leave the City for vacation or for trips back to their home country * Driver for at least 3 years\*; * Driving schedule does not include overnight shifts, nor does driver have an additional job overnight; * Own a smart phone (in order to collect heart rate variability data) * Should self-report at least Very well level of English fluency (according to the standard US census question) * Have working cigarette lighter receptacle/socket inside taxi cab \*The requirement to have worked at least 3 years in the U.S. should minimize any acute health effects/disease due to high levels of contaminants associated with country of origin

Exclusion criteria

Drivers: * Smoker or uses smokeless tobacco products; * Resides in a smoking household (where 1 or more household members smoke); * Has a sleep disorder (including insomnia, delayed sleep phase syndrome (DSPS), narcolepsy, night terror, sleep apnea, sleep walking); * Has a current or previous diagnosis of any type of cancer; * Has a diagnosis of an inflammatory, autoimmune, or chronic infectious disease (including rheumatoid arthritis, lupus, chronic liver disease, multiple sclerosis, fibromyalgia, inflammatory bowel disease, psoriasis, HIV); * Has a serious cardiopulmonary medical condition (including cardiovascular disease, congestive heart failure (CHF), chronic obstructive pulmonary disease (COPD), restrictive lung disease, interstitial lung disease, asthma, acute or chronic bronchitis, cystic fibrosis, pneumonia, tuberculosis, pneumoconiosis, pulmonary hypertension, pulmonary embolism, pleural effusion, pneumothorax, obesity hypoventilation syndrome, neuromuscular lung disease). * Self reports -well‖ level of English fluency and indicates a preference for an interpreter.

Design outcomes

Primary

MeasureTime frameDescription
Collect Preliminary Data on In-vehicle Excess Particulate Matter (PM) Exposure2 yearsmonitor/report the PM levels as time-averaged sample (hourly averages) that will be monitored at work site and at homes across all groups

Countries

United States

Participant flow

Participants by arm

ArmCount
Intervention Group
During the first 2 weeks, measurements (e.g. biological markers and air monitoring) will be taken under usual conditions. At the end of the initial two weeks, portable HEPA air purifiers (136) will be placed in the Intervention Group drivers' cars and the air monitoring and biological parameters will be repeated for another 2-week period, to determine changes in PM levels and physiological measurements as a result of this targeted intervention. HEPA air purifier: air purifiers to remove PM and volatile organic compounds will be placed in drivers cars questionnaires Log-book: PM and biological measurements Urine sample: PAH (Polycyclic Aromatic Hydrocarbon) will be assessed via urine sample collection of Urinary 1 hydroxy pyrene and particulate matter collected via Polyurethane Foam Filter (PUF) sampler
17
Wait-list Control Group
During the first 2 weeks, measurements (e.g. biological markers and air monitoring) will be taken under usual conditions. The Wait-list Control Group drivers will not receive a HEPA air purifier at this time, but will also have the air monitoring and biological parameters repeated for another 2 weeks. At the end of the 1 month period of measurements for both groups of drivers, the Wait-list drivers will then receive a HEPA air purifier, so that they may also potentially benefit from the intervention being tested in this study, but no further measurements will be taken. HEPA air purifier: air purifiers to remove PM and volatile organic compounds will be placed in drivers cars questionnaires Log-book: PM and biological measurements Urine sample: PAH (Polycyclic Aromatic Hydrocarbon) will be assessed via urine sample collection of Urinary 1 hydroxy pyrene and particulate matter collected via Polyurethane Foam Filter (PUF) sampler
16
Peer Non-driver
Peer non-driver (peer is matched to driver assigned to the HEPA filter intervention group)
6
Total39

Baseline characteristics

CharacteristicIntervention GroupTotalPeer Non-driverWait-list Control Group
Age, Continuous46.5 years48.1 years48.7 years49.5 years
Ethnicity (NIH/OMB)
Hispanic or Latino
1 Participants4 Participants0 Participants3 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
16 Participants35 Participants6 Participants13 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
2 Participants4 Participants0 Participants2 Participants
Race (NIH/OMB)
Black or African American
12 Participants29 Participants6 Participants11 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
1 Participants3 Participants0 Participants2 Participants
Race (NIH/OMB)
White
2 Participants3 Participants0 Participants1 Participants
Region of Enrollment
United States
17 Participants39 Participants6 Participants16 Participants
Sex: Female, Male
Female
0 Participants0 Participants0 Participants0 Participants
Sex: Female, Male
Male
17 Participants39 Participants6 Participants16 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
deaths
Total, all-cause mortality
0 / 170 / 160 / 6
other
Total, other adverse events
0 / 170 / 160 / 6
serious
Total, serious adverse events
0 / 170 / 160 / 6

Outcome results

Primary

Collect Preliminary Data on In-vehicle Excess Particulate Matter (PM) Exposure

monitor/report the PM levels as time-averaged sample (hourly averages) that will be monitored at work site and at homes across all groups

Time frame: 2 years

Population: Data were not collected

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026