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Monitoring Environmental Exposures and Behavioral Change

Utah System of Higher Education (USHE) logo

Utah System of Higher Education (USHE)

Status

Completed

Conditions

Environmental Exposure
Risk Behavior, Health
Risk Reduction

Treatments

Device: Real-Time Exposure Feedback

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05338242
R21NArapaho
R21ES032137 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The goal of this study is to examine what effect real-time feedback on particulate matter (PM) air pollution levels has on risk recognition and behavior. The hypothesis is that real-time exposure feedback will change perceptions of risk and increase behaviors that avoid exposure to environmental risks. At least one representative household member in participating households will complete a questionnaire to fully understand environmental concerns, risk perceptions, and related behaviors. Half of the households will have PM monitors that continuously display real-time concentrations and an indication of the hazard level. The other participants will have the same device but it will only display the date and time. All participants will then be surveyed again: (a) immediately after sampling is complete (i.e., when the devices are removed from the home), (b) after 3 months and, (c) after 6 months. The goal of repeated surveys is to determine changing understanding of risks, how participating in research and/or receiving real-time exposure data may have changed participant behavior, and what concerns they continue to have. The questionnaire will include questions with categorical and/or quantitative answers (e.g., frequency of specific behaviors) so that changes in risk perception and behavior can be effectively analyzed.

Enrollment

30 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Participants must live in a household where at least one adult is a member of the N. Arapaho tribe who is a Primary Participant in the related exposure assessment study.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

30 participants in 2 patient groups

Real-Time Feedback
Experimental group
Description:
Participants will receive real-time exposure monitors that continuously display real-time air concentration information and a color-coded designation for the current risk level.
Treatment:
Device: Real-Time Exposure Feedback
No Feedback
No Intervention group
Description:
Participants will have exposure levels monitored by the same device, but it will only display the date/time and will not provide real-time feedback.

Trial contacts and locations

1

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Central trial contact

Darrah K Sleeth, PhD; Scott Collingwood, PhD

Data sourced from clinicaltrials.gov

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