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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05338242
Other study ID # R21NArapaho
Secondary ID R21ES032137
Status Recruiting
Phase N/A
First received
Last updated
Start date July 28, 2022
Est. completion date April 2024

Study information

Verified date November 2023
Source University of Utah
Contact Darrah K Sleeth, PhD
Phone 801-585-3587
Email darrah.sleeth@hsc.utah.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Recruiting
Enrollment 72
Est. completion date April 2024
Est. primary completion date March 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design


Intervention

Device:
Real-Time Exposure Feedback
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.

Locations

Country Name City State
United States University of Utah Salt Lake City Utah

Sponsors (2)

Lead Sponsor Collaborator
University of Utah National Institute of Environmental Health Sciences (NIEHS)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Behaviors Related to Reduction in Exposure Outcomes will be measured as a change in how often (frequency) behaviors related to reduction in exposure occur At removal of device
Primary Behaviors Related to Reduction in Exposure Outcomes will be measured as a change in how often (frequency) behaviors related to reduction in exposure occur 3 months after removal of device
Primary Behaviors Related to Reduction in Exposure Outcomes will be measured as a change in how often (frequency) behaviors related to reduction in exposure occur 6 months after removal of device
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